| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:14743-15257 | |||||
| chrX:11111042-11111365 | Common:3; Rare:68 | ||||
| chrX:13734577-13734811 | Common:3; Rare:75; Clinvar (benign):1 | ||||
| chrX:14029886-14030009 | Common:2; Rare:35 | ||||
| chrX:14873037-14873338 | Common:1; Rare:57 | ||||
| chrX:15493187-15493424 | Common:1; Rare:44 | ||||
| chrX:16719444-16719683 | Rare:70 | ||||
| chrX:19670887-19671066 | Rare:31 | ||||
| chrX:20141761-20142095 | Common:1; Rare:74 | ||||
| chrX:23743226-23743478 | Common:7; Rare:50 | ||||
| chrX:44542828-44543089 | Common:1; Rare:50 | ||||
| chrX:46545397-46545520 | Rare:21 | ||||
| chrX:47144654-47144810 | Rare:27 | ||||
| chrX:47145097-47145273 | Rare:28 | ||||
| chrX:47482545-47482664 | Common:5; Rare:26; Clinvar:2 |