ID: 130001967 | ATAC-STARR-seq lymphoblastoid active region 28514 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86282389..86282538) | | |
ID: 130001966 | ATAC-STARR-seq lymphoblastoid silent region 19996 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86281919..86282218) | | |
ID: 130001965 | ATAC-STARR-seq lymphoblastoid silent region 19995 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86202466..86202515) | | |
ID: 130001964 | ATAC-STARR-seq lymphoblastoid silent region 19994 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86099450..86099769) | | |
ID: 130001963 | ATAC-STARR-seq lymphoblastoid silent region 19991 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (85941050..85941729) | | |
ID: 127815069 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr9:88801905-88802559 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86186990..86187644) | | |
ID: 127815068 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:88771625-88772258 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86156710..86157343) | | |
ID: 127815067 | H3K27ac hESC enhancer GRCh37_chr9:88713914-88714414 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86098999..86099499) | | |
ID: 127815066 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:88680249-88681249 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86065334..86066334) | | |
ID: 127815065 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:88679748-88680248 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86064833..86065333) | | |
ID: 127815064 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:88677599-88678515 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86062684..86063600) | | |
ID: 127815063 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:88650825-88651760 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86035910..86036845) | | |
ID: 126860667 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr9:88761003-88762202 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86146088..86147287) | | |
ID: 126860666 | BRD4-independent group 4 enhancer GRCh37_chr9:88693798-88694997 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86078883..86080082) | | |
ID: 124902194 | uncharacterized LOC124902194 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86278217..86282081, complement) | | |
ID: 124310577 | Sharpr-MPRA regulatory region 1717 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86176014..86176308) | | |
ID: 124310576 | Sharpr-MPRA regulatory region 3020 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86093754..86094048) | | |
ID: 106479213 | RN7SK pseudogene 264 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86258425..86258646, complement) | | |
ID: 101927623 | uncharacterized LOC101927623 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86127540..86157086) | | |
ID: 100287212 | allregulin pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86132624..86135008) | | |