| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:85003773-85003918 | Common:1; Rare:31 | ||||
| chrX:85243697-85244191 | Common:4; Rare:107; Clinvar (benign):1 | ||||
| chrX:86047494-86047636 | Common:1; Rare:35 | ||||
| chrX:91434766-91434866 | Rare:24 | ||||
| chrX:91434961-91435008 | Rare:6 | ||||
| chrX:91435013-91435048 | Rare:3 | ||||
| chrX:91435086-91435125 | Rare:7 | ||||
| chrX:93673528-93673790 | Common:1; Rare:43 | ||||
| chrX:93673962-93674192 | Rare:30 | ||||
| chrX:100820220-100820432 | Common:2; Rare:52 | ||||
| chrX:101052072-101052179 | Rare:11 | ||||
| chrX:101390780-101391102 | Rare:97 | ||||
| chrX:101407956-101408282 | Common:2; Rare:49; Clinvar (benign):2 | ||||
| chrX:101418120-101418290 | Common:1; Rare:31 | ||||
| chrX:101485109-101485504 | Rare:56 |