ID: 127898550 | H3K27ac hESC enhancer GRCh37_chrX:154255797-154256700 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155027522..155028425) | | |
ID: 126863349 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chrX:154195537-154196736 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154967262..154968461) | | |
ID: 125467795 | Sharpr-MPRA regulatory region 4209 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155007074..155007368) | | |
ID: 121627986 | H3K4me1 hESC enhancer GRCh37_chrX:154285543-154286044 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155057268..155057769) | | |
ID: 106146143 | int1h-1 recombination region [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155006107..155007182) | | |
ID: 100419792 | ZNF622 pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154919433..154920182, complement) | | |
ID: 65991 | FUN14 domain containing 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155026844..155060304) | DC44, HCBP6, HCC3, PD03104 | 301042 |
ID: 2157 | coagulation factor VIII [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154835792..155022723, complement) | AHF, DXS1253EB, F8C, FVIII, HEMA, THPH13, F8 | 300841 |