ID: 130068271 | ATAC-STARR-seq lymphoblastoid silent region 20833 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (49053686..49053985) | | |
ID: 130068270 | ATAC-STARR-seq lymphoblastoid active region 29627 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (49002273..49002382) | | |
ID: 129664949 | ReSE screen-validated silencer GRCh37_chrX:48840212-48840468 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (48983800..48984056) | | |
ID: 127897543 | H3K27ac hESC enhancer GRCh37_chrX:48900209-48901072 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (49042683..49043546) | | |
ID: 125467748 | Sharpr-MPRA regulatory region 12141 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (48961588..48961980) | | |
ID: 121627970 | Sharpr-MPRA regulatory region 13918 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (49053340..49053635) | | |
ID: 119407414 | CRISPRi-FlowFISH-validated PQBP1 regulatory element 4 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (49047157..49047736) | | |
ID: 119407413 | CRISPRi-FlowFISH-validated HDAC6 regulatory element 4 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (49003655..49004155) | | |
ID: 114022707 | Sharpr-MPRA regulatory region 9113 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (48997017..48997311) | | |
ID: 113875032 | Sharpr-MPRA regulatory region 2669 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (49039844..49040138) | | |
ID: 106481407 | RNA, U6 small nuclear 722, pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (48959179..48959282, complement) | | |
ID: 90060 | coiled-coil domain containing 120 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (49053572..49069858) | JM11 | 300947 |
ID: 56850 | GRIP1 associated protein 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (48973723..49002264, complement) | GRASP-1 | 300408 |
ID: 7030 | transcription factor binding to IGHM enhancer 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (49028726..49043357, complement) | MRXSPF, RCCP2, RCCX1, TFEA, bHLHe33 | 314310 |
ID: 3750 | potassium voltage-gated channel subfamily D member 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (48961380..48971844, complement) | KV4.1 | 300281 |