| ID: 127408963 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:42377053-42377557 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42337454..42337958) | | |
| ID: 127408962 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:42376548-42377052 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42336949..42337453) | | |
| ID: 127408961 | H3K27ac hESC enhancer GRCh37_chr7:42276552-42277533 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42236953..42237934) | | |
| ID: 127408960 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:42267911-42268690 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42228312..42229091) | | |
| ID: 127408959 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr7:42261657-42262165 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42222058..42222566) | | |
| ID: 127408958 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr7:42232601-42233188 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42193002..42193589) | | |
| ID: 127408957 | NANOG hESC enhancer GRCh37_chr7:42178252-42178762 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42138653..42139163) | | |
| ID: 127408956 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:42131129-42131824 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42091530..42092225) | | |
| ID: 127408955 | OCT4-NANOG hESC enhancer GRCh37_chr7:42105443-42106096 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42065844..42066497) | | |
| ID: 127408954 | H3K4me1 hESC enhancer GRCh37_chr7:42068797-42069297 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42029198..42029698) | | |
| ID: 126860014 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr7:41748736-41749935 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (41709138..41710337) | | |
| ID: 124901618 | uncharacterized LOC124901618 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (41929597..41933590, complement) | | |
| ID: 110121152 | VISTA enhancer hs1586 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42146003..42147909) | | |
| ID: 110121030 | VISTA enhancer hs1213 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42213232..42214961) | | |
| ID: 110120590 | VISTA enhancer hs111 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42152129..42154039) | | |
| ID: 105375249 | uncharacterized LOC105375249 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42326302..42338336, complement) | | |
| ID: 100131183 | high mobility group nucleosomal binding domain 2 pseudogene 30 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (42113256..42114439) | | |
| ID: 285954 | INHBA antisense RNA 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (41693919..41779378) | | |
| ID: 3624 | inhibin subunit beta A [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (41685114..41705406, complement) | EDF, FRP | 147290 |
| ID: 2737 | GLI family zinc finger 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (41960949..42264268, complement) | ACLS, GCPS-190, GLI3FL, PAP-A, PAPA, PAPA1, PAPB, PHS, PPDIV, GLI3 | 165240 |