| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:38220826-38221047 | Rare:49 | ||||
| chrX:38801187-38801525 | Common:2; Rare:70 | ||||
| chrX:40735520-40735716 | Rare:56 | ||||
| chrX:41085552-41085809 | Rare:56 | ||||
| chrX:41333466-41333618 | Rare:24 | ||||
| chrX:41333773-41334652 | Common:8; Rare:267 | ||||
| chrX:41334976-41335109 | Rare:19 | ||||
| chrX:46545115-46545602 | Common:2; Rare:83; Clinvar (benign):2 | ||||
| chrX:46836649-46837197 | Common:1; Rare:109; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chrX:47144668-47144853 | Common:1; Rare:31 | ||||
| chrX:47145086-47145403 | Rare:56 | ||||
| chrX:47175134-47175460 | Rare:32 | ||||
| chrX:47193791-47194012 | Common:1; Rare:33; Clinvar:1 | ||||
| chrX:47202333-47202811 | Common:1; Rare:115; Clinvar:1; Clinvar (benign):3 | ||||
| chrX:47226646-47226901 | Rare:37 |