| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:30653162-30653504 | Common:2; Rare:87 | ||||
| chrX:37349111-37349395 | Common:2; Rare:37 | ||||
| chrX:37847490-37847677 | Common:1; Rare:45 | ||||
| chrX:38327472-38327711 | Rare:64 | ||||
| chrX:41085196-41085498 | Common:3; Rare:88 | ||||
| chrX:41333374-41333628 | Rare:45 | ||||
| chrX:41333876-41334296 | Common:6; Rare:110 | ||||
| chrX:41334318-41334657 | Common:2; Rare:125 | ||||
| chrX:41334999-41335113 | Rare:15 | ||||
| chrX:41688943-41689071 | Common:1; Rare:10 | ||||
| chrX:44343616-44343739 | Common:4; Rare:42 | ||||
| chrX:44542815-44543061 | Common:1; Rare:50 | ||||
| chrX:46545377-46545538 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chrX:47078701-47078977 | Common:2; Rare:40 | ||||
| chrX:47144647-47144837 | Common:1; Rare:32 |