| ID: 130068895 | ATAC-STARR-seq lymphoblastoid active region 30074 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155070764..155071063) | | |
| ID: 130068894 | ATAC-STARR-seq lymphoblastoid silent region 21121 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155027025..155027344) | | |
| ID: 130068893 | ATAC-STARR-seq lymphoblastoid silent region 21120 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155026665..155026754) | | |
| ID: 130068892 | ATAC-STARR-seq lymphoblastoid active region 30073 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154981060..154981109) | | |
| ID: 130068891 | ATAC-STARR-seq lymphoblastoid active region 30072 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154980910..154980959) | | |
| ID: 127898551 | H3K27ac hESC enhancer GRCh37_chrX:154299323-154300044 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155071048..155071769) | | |
| 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: 100272147 | C-X9-C motif containing 4 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155061622..155071136, complement) | C6.1B, MTCP1, MTCP1B, MTCP1NB, p8, p8MTCP1 | 301088 |
| ID: 553820 | eukaryotic translation elongation factor 1 alpha 1 pseudogene 31 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154908824..154919212, complement) | | |
| ID: 65991 | FUN14 domain containing 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155026844..155060304) | DC44, HCBP6, HCC3, PD03104 | 301042 |
| ID: 4515 | mature T cell proliferation 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155064034..155071136, complement) | P13MTCP1, TCL1C, p8MTCP1 | 300116 |
| ID: 2157 | coagulation factor VIII [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154835792..155022723, complement) | AHF, DXS1253EB, F8C, FVIII, HEMA, THPH13, F8 | 300841 |