| ID: 127824158 | H3K4me1 hESC enhancer GRCh37_chr12:51346409-51346909 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50952626..50953126) | | |
| ID: 127824157 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:51319135-51319678 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50925352..50925895) | | |
| ID: 116268439 | CRISPRi-validated cis-regulatory element chr12.1615 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50901497..50902266) | | |
| ID: 112163601 | Sharpr-MPRA regulatory region 4642 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50933826..50934120) | | |
| ID: 106481204 | RNA, U6 small nuclear 87, pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (51014134..51014241, complement) | | |
| ID: 100147826 | RNA, U7 small nuclear 39 pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (51010999..51011057) | U7.39 | |
| ID: 613227 | HIG1 hypoxia inducible domain family member 1C [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50931110..50972592) | GM921 | 620803 |
| ID: 25840 | thiol methyltransferase 1A [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50925015..50932508) | AAM-B, AAMB, METTL7A | 618338 |
| ID: 4891 | solute carrier family 11 member 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50952263..51028886, complement) | AHMIO1, DCT1, DMT1, NRAMP2 | 600523 |