ID: 127815783 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:124132533-124133493 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121370255..121371215) | | |
ID: 127815782 | H3K4me1 hESC enhancer GRCh37_chr9:124089303-124090216 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121327025..121327938) | | |
ID: 127815781 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:124061747-124062407 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121299469..121300129) | | |
ID: 127815780 | H3K4me1 hESC enhancer GRCh37_chr9:124056667-124057289 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121294389..121295011) | | |
ID: 127815779 | H3K4me1 hESC enhancer GRCh37_chr9:124047035-124047535 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121284757..121285257) | | |
ID: 127815778 | H3K4me1 hESC enhancer GRCh37_chr9:124023585-124024084 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121261307..121261806) | | |
ID: 127815777 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:123983210-123983860 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121220932..121221582) | | |
ID: 127815776 | H3K27ac hESC enhancer GRCh37_chr9:123963761-123964260 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121201321..121202020) | | |
ID: 127815775 | NANOG hESC enhancer GRCh37_chr9:123883693-123884194 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121121415..121121916) | | |
ID: 126860753 | MED14-independent group 3 enhancer GRCh37_chr9:124048350-124049549 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121286072..121287271) | | |
ID: 126860752 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:124043752-124044951 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121281474..121282673) | | |
ID: 124902357 | uncharacterized LOC124902357 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121176681..121176843, complement) | | |
ID: 124310633 | Sharpr-MPRA regulatory region 178 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121287411..121287705) | | |
ID: 106480492 | RNA, 7SL, cytoplasmic 181, pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121203172..121203435) | | |
ID: 102723324 | uncharacterized LOC102723324 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121369893..121463371) | | |
ID: 645482 | ATPase H+ transporting V1 subunit B2 pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121238674..121240079, complement) | | |
ID: 57000 | GSN antisense RNA 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121280768..121285530, complement) | C9orf31, MOST2 | |
ID: 51552 | RAB14, member RAS oncogene family [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121178133..121201869, complement) | FBP, RAB-14 | 612673 |
ID: 11064 | centriolin [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121074955..121177610) | CEP1, CEP110, FAN, bA165P4.1 | 605496 |
ID: 2934 | gelsolin [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (121201483..121332842) | ADF, AGEL | 137350 |