| ID: 130068414 | ATAC-STARR-seq lymphoblastoid silent region 20896 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71254706..71254755) | | |
| ID: 130068413 | ATAC-STARR-seq lymphoblastoid silent region 20895 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71254636..71254685) | | |
| ID: 130068412 | ATAC-STARR-seq lymphoblastoid active region 29741 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71198336..71198515) | | |
| ID: 130068411 | ATAC-STARR-seq lymphoblastoid active region 29740 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71196060..71196189) | | |
| ID: 130068410 | ATAC-STARR-seq lymphoblastoid active region 29739 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71182383..71182472) | | |
| ID: 130068409 | ATAC-STARR-seq lymphoblastoid active region 29738 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71181933..71181982) | | |
| ID: 129664971 | ReSE screen-validated silencer GRCh37_chrX:70365507-70365762 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71145657..71145912) | | |
| ID: 127897768 | H3K4me1 hESC enhancer GRCh37_chrX:70373033-70373532 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71153183..71153682) | | |
| ID: 127897767 | H3K4me1 hESC enhancer GRCh37_chrX:70367884-70368430 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71148034..71148580) | | |
| ID: 127897766 | H3K4me1 hESC enhancer GRCh37_chrX:70367337-70367883 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71147487..71148033) | | |
| ID: 126863275 | BRD4-independent group 4 enhancer GRCh37_chrX:70342400-70343599 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71122550..71123749) | | |
| ID: 124905197 | uncharacterized LOC124905197 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71142546..71152320, complement) | | |
| ID: 113875038 | Sharpr-MPRA regulatory region 11812 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71182039..71182333) | | |
| ID: 107985688 | uncharacterized LOC107985688 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71183382..71198193, complement) | | |
| ID: 105373247 | uncharacterized LOC105373247 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71254808..71272792) | | |
| ID: 54413 | neuroligin 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71144841..71175307) | HNL3 | 300336 |
| ID: 9968 | mediator complex subunit 12 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71118596..71142450) | ARC240, CAGH45, FGS1, HDKR, HOPA, KtoS, OHDOX, OKS, OPA1, TNRC11, TRAP230, MED12 | 300188 |
| ID: 9203 | zinc finger MYM-type containing 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71239624..71255290, complement) | DXS6673E, MYM, XFIM, XLID112, ZNF198L2, ZNF261 | 300061 |
| ID: 2705 | gap junction protein beta 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71215239..71225516) | CMTX, CMTX1, CX32 | 304040 |