ID: 127882544 | H3K4me1 hESC enhancer GRCh37_chr9:130328804-130329344 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127566525..127567065) | | |
ID: 127816068 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:130332049-130332588 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127569770..127570309) | | |
ID: 127816067 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:130331508-130332048 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127569137..127569769) | | |
ID: 127816066 | H3K4me1 hESC enhancer GRCh37_chr9:130325437-130326140 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127563158..127563861) | | |
ID: 127816065 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:130324732-130325436 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127562453..127563157) | | |
ID: 127816064 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:130323322-130324026 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127561043..127561747) | | |
ID: 127816063 | H3K4me1 hESC enhancer GRCh37_chr9:130314335-130314834 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127552056..127552555) | | |
ID: 127816062 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:130293634-130294194 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127531355..127531915) | | |
ID: 127816061 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:130287309-130287861 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127525030..127525582) | | |
ID: 127816060 | H3K4me1 hESC enhancer GRCh37_chr9:130286169-130286668 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127523890..127524389) | | |
ID: 127816059 | H3K4me1 hESC enhancer GRCh37_chr9:130285667-130286168 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127523388..127523889) | | |
ID: 127816058 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:130266531-130267404 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127504252..127505125) | | |
ID: 127816057 | H3K4me1 hESC enhancer GRCh37_chr9:130262849-130263350 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127500570..127501071) | | |
ID: 124902277 | uncharacterized LOC124902277 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127587489..127592587) | | |
ID: 124902276 | uncharacterized LOC124902276 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127579278..127582579) | | |
ID: 113839509 | Sharpr-MPRA regulatory region 10550 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127576170..127576464) | | |
ID: 113839508 | Sharpr-MPRA regulatory region 14561 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127555646..127556364) | | |
ID: 108281127 | FAM129B intron CAGE-defined low expression enhancer [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127567021..127567606) | | |
ID: 105376281 | uncharacterized LOC105376281 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127536585..127542618, complement) | | |
ID: 90678 | leucine rich repeat and sterile alpha motif containing 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127451486..127503501) | CMT2P, RIFLE, TAL | 610933 |