| ID: 127827176 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:20937332-20937836 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20469173..20469677) | | |
| ID: 127827175 | H3K27ac hESC enhancer GRCh37_chr14:20929880-20930845 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20461721..20462686) | | |
| ID: 127827174 | H3K27ac hESC enhancer GRCh37_chr14:20928913-20929879 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20460754..20461720) | | |
| ID: 127827173 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:20903872-20904781 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20435713..20436622) | | |
| ID: 127827172 | H3K4me1 hESC enhancer GRCh37_chr14:20897153-20897785 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20428994..20429626) | | |
| ID: 127827171 | H3K27ac hESC enhancer GRCh37_chr14:20880498-20881414 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20412339..20413255) | | |
| ID: 127827170 | H3K27ac hESC enhancer GRCh37_chr14:20679982-20680782 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20211823..20212623) | | |
| ID: 126861879 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr14:20868788-20869987 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20400629..20401828) | | |
| ID: 126861878 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr14:20763215-20764414 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20295056..20296255) | | |
| ID: 124958010 | Sharpr-MPRA regulatory region 9617 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20457090..20457384) | | |
| ID: 124903278 | uncharacterized LOC124903278 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (19902461..19948734, complement) | | |
| ID: 109616976 | small nucleolar RNA, H/ACA box 79B [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20323179..20323326, complement) | | |
| ID: 107372315 | OSGEP/APEX1 bi-directional promoter region [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20451644..20455489) | | |
| ID: 106480347 | general transcription factor IIi pseudogene 22 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20173632..20173813, complement) | | |
| ID: 100873637 | RNA, 5S ribosomal pseudogene 382 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20414987..20415098) | RN5S382 | |
| ID: 100873636 | RNA, 5S ribosomal pseudogene 380 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20090130..20090227) | RN5S380 | |
| ID: 100422510 | solute carrier family 12 member 3 pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20438504..20439449) | | |
| ID: 100422289 | PSMB7 pseudogene 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20149235..20149872) | | |
| ID: 100421751 | ATPase Na+/K+ transporting subunit beta 3 pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (19907999..19908645, complement) | | |
| ID: 100113391 | small nucleolar RNA, C/D box 126 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20326441..20326539, complement) | MIR1201, MIRN1201 | |