| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119398996-119399420 | Common:8; Rare:153 | ||||
| chrX:119468184-119468609 | Common:7; Rare:221 | ||||
| chrX:119469050-119469270 | Rare:103 | ||||
| chrX:119574345-119574624 | Rare:110 | ||||
| chrX:119606352-119606562 | Common:2; Rare:81 | ||||
| chrX:119693146-119693620 | Common:5; Rare:150 | ||||
| chrX:119757740-119758180 | Common:3; Rare:69 | ||||
| chrX:119791574-119791995 | Common:2; Rare:187 | ||||
| chrX:119871638-119872008 | Common:3; Rare:135; Clinvar (benign):7 | ||||
| chrX:119943603-119943862 | Rare:89 | ||||
| chrX:120250726-120250963 | Common:4; Rare:47 | ||||
| chrX:120559880-120560190 | Rare:83 | ||||
| chrX:120560687-120561185 | Rare:148 | ||||
| chrX:120561330-120561674 | Common:2; Rare:116 | ||||
| chrX:120603818-120604204 | Rare:139 |