ID: 127816740 | H3K4me1 hESC enhancer GRCh37_chr9:138695080-138695746 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135803234..135803900) | | |
ID: 127816739 | H3K4me1 hESC enhancer GRCh37_chr9:138675789-138676289 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135783943..135784443) | | |
ID: 127816738 | H3K4me1 hESC enhancer GRCh37_chr9:138639213-138639970 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135747367..135748124) | | |
ID: 127816737 | H3K4me1 hESC enhancer GRCh37_chr9:138619907-138620844 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135728061..135728998) | | |
ID: 127816736 | H3K4me1 hESC enhancer GRCh37_chr9:138615694-138616271 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135723848..135724425) | | |
ID: 127816735 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:138586423-138586937 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135694577..135695091) | | |
ID: 121811720 | Sharpr-MPRA regulatory region 6734 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135850723..135851017) | | |
ID: 113839538 | Sharpr-MPRA regulatory region 14740 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135718623..135718917) | | |
ID: 107987140 | uncharacterized LOC107987140 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135787929..135792041, complement) | | |
ID: 105376318 | uncharacterized LOC105376318 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135678045..135679562) | | |
ID: 105376317 | uncharacterized LOC105376317 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135675200..135685111, complement) | | |
ID: 402381 | spermatogenesis and oogenesis specific basic helix-loop-helix 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135693407..135702112, complement) | C9orf157, NOHLH, ODG5, SPATA27, SPGF32, TEB2, bA100C15.3, bHLHe80 | 610224 |
ID: 157922 | calmodulin regulated spectrin associated protein 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135808487..135907546, complement) | CDCBM12 | 613774 |
ID: 57582 | potassium sodium-activated channel subfamily T member 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135702185..135795502) | DEE14, EIEE14, ENFL5, KCa4.1, SLACK, Slo2.2, bA100C15.2 | 608167 |