Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:23907712-23907836 | Common:1; Rare:31 | ||||
chrX:23907844-23908076 | Rare:45 | ||||
chrX:24054675-24055028 | Rare:83 | ||||
chrX:24149638-24149778 | Rare:27 | ||||
chrX:31266905-31267066 | Common:1; Rare:46 | ||||
chrX:33211487-33211699 | Rare:37; Clinvar:2; Clinvar (benign):1 | ||||
chrX:38220737-38221038 | Common:1; Rare:82 | ||||
chrX:38327472-38327682 | Rare:53 | ||||
chrX:40735850-40736033 | Common:1; Rare:30 | ||||
chrX:43656146-43656366 | Rare:45 | ||||
chrX:44542803-44543160 | Common:1; Rare:74 | ||||
chrX:46545385-46545566 | Rare:42 | ||||
chrX:47144636-47144839 | Common:1; Rare:34 | ||||
chrX:47145089-47145285 | Rare:30 | ||||
chrX:47232897-47233026 | Rare:36 |