ID: 127403179 | H3K27ac hESC enhancer GRCh37_chr5:76787603-76788526 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77491778..77492701) | | |
ID: 127403178 | NANOG-H3K4me1 hESC enhancer GRCh37_chr5:76672412-76673040 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77376587..77377215) | | |
ID: 127403177 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:76618089-76618784 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77322264..77322959) | | |
ID: 127403176 | H3K4me1 hESC enhancer GRCh37_chr5:76468397-76468898 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77172572..77173073) | | |
ID: 127403175 | H3K4me1 hESC enhancer GRCh37_chr5:76383973-76384573 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77088148..77088748) | | |
ID: 127403174 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:76383370-76383972 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77087545..77088147) | | |
ID: 127403173 | H3K27ac hESC enhancer GRCh37_chr5:76382768-76383369 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77086943..77087544) | | |
ID: 127403172 | H3K27ac hESC enhancer GRCh37_chr5:76326467-76327046 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77030642..77031221) | | |
ID: 124901009 | uncharacterized LOC124901009 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77481967..77485541, complement) | | |
ID: 124901008 | uncharacterized LOC124901008 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77127708..77131128, complement) | | |
ID: 121079946 | Sharpr-MPRA regulatory region 15273 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77144564..77144858) | | |
ID: 100419950 | high mobility group box 1 pseudogene 35 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77146568..77147157) | | |
ID: 100270912 | ribosomal protein S2 pseudogene 24 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77545371..77546303) | RPS2_11_579 | |
ID: 728723 | ZBED3 antisense RNA 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77086715..77149301) | lnc13728 | |
ID: 677828 | small nucleolar RNA, H/ACA box 47 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77080434..77080571, complement) | HBI-115 | |
ID: 84327 | zinc finger BED-type containing 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77072072..77087285, complement) | | 615250 |
ID: 55255 | WD repeat domain 41 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77430933..77620577, complement) | MSTP048 | 617502 |
ID: 55109 | angiogenic factor with G-patch and FHA domains 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77030404..77065234) | GPATC7, GPATCH7, HSU84971, HUS84971, VG5Q | 608464 |
ID: 8622 | phosphodiesterase 8B [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77086715..77428256) | ADSD, PPNAD3 | 603390 |
ID: 541 | aldehyde dehydrogenase 7 family member A1 pseudogene 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (77290184..77291997) | ATQL1 | |