| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:37847506-37847677 | Common:1; Rare:43 | ||||
| chrX:38220766-38220929 | Rare:41 | ||||
| chrX:38220954-38221044 | Rare:25 | ||||
| chrX:41085220-41085476 | Common:3; Rare:74 | ||||
| chrX:41333693-41333942 | Common:4; Rare:64 | ||||
| chrX:41334438-41334647 | Common:2; Rare:80 | ||||
| chrX:41689013-41689070 | Common:1; Rare:6 | ||||
| chrX:44542792-44543034 | Common:1; Rare:49 | ||||
| chrX:46545377-46545547 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chrX:47144492-47144756 | Common:1; Rare:64; Clinvar (benign):1 | ||||
| chrX:47145089-47145301 | Rare:31 | ||||
| chrX:47218700-47218732 | Rare:14 | ||||
| chrX:47233310-47233456 | Rare:24 | ||||
| chrX:47482578-47482665 | Common:5; Rare:19; Clinvar:2 | ||||
| chrX:47482928-47483032 | Rare:18 |