| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:43973342-43973784 | Common:4; Rare:107; Clinvar (benign):2 | ||||
| chrX:44542845-44543106 | Common:1; Rare:52 | ||||
| chrX:44872873-44873219 | Common:1; Rare:59 | ||||
| chrX:46446490-46446930 | Common:2; Rare:66 | ||||
| chrX:46447087-46447335 | Rare:44 | ||||
| chrX:46545374-46545599 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chrX:46573486-46574252 | Common:4; Rare:174 | ||||
| chrX:46836681-46836982 | Rare:48 | ||||
| chrX:46912040-46912350 | Rare:53 | ||||
| chrX:46912879-46914054 | Common:6; Rare:257 | ||||
| chrX:47144372-47144509 | Common:8; Rare:39 | ||||
| chrX:47144650-47144821 | Common:1; Rare:29 | ||||
| chrX:47144994-47145299 | Rare:40 | ||||
| chrX:47190591-47190879 | Rare:41 | ||||
| chrX:47191359-47191759 | Rare:85 |