| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48521561-48521889 | Common:1; Rare:53 | ||||
| chrX:48574390-48574558 | Common:1; Rare:63 | ||||
| chrX:48574869-48574981 | Rare:33 | ||||
| chrX:48597638-48597863 | Common:1; Rare:26 | ||||
| chrX:48911637-48911715 | Rare:19; Clinvar (benign):3 | ||||
| chrX:48958320-48958618 | Rare:70 | ||||
| chrX:49002220-49002564 | Common:2; Rare:59 | ||||
| chrX:49073991-49074183 | Rare:47 | ||||
| chrX:49079849-49079942 | Rare:15 | ||||
| chrX:49171755-49172031 | Common:4; Rare:38 | ||||
| chrX:49186283-49186482 | Common:1; Rare:34 | ||||
| chrX:53225186-53225502 | Common:2; Rare:100 | ||||
| chrX:53422605-53422906 | Common:2; Rare:86; Clinvar (benign):1 | ||||
| chrX:53434334-53434599 | Common:1; Rare:55 | ||||
| chrX:53686317-53686422 | Rare:19 |