| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119791590-119791999 | Common:2; Rare:108 | ||||
| chrX:119871374-119871485 | Rare:14 | ||||
| chrX:119871585-119871969 | Common:2; Rare:72; Clinvar (benign):3 | ||||
| chrX:119943607-119943858 | Rare:45 | ||||
| chrX:120250756-120250905 | Common:3; Rare:27 | ||||
| chrX:120560468-120560860 | Rare:62; Clinvar:2 | ||||
| chrX:120561070-120561161 | Rare:14 | ||||
| chrX:120561376-120561707 | Common:1; Rare:52 | ||||
| chrX:120603797-120604008 | Rare:40 | ||||
| chrX:120604037-120604167 | Rare:27 | ||||
| chrX:120604660-120604776 | Rare:10 | ||||
| chrX:123732988-123733156 | Rare:31; Clinvar (benign):1 | ||||
| chrX:123859689-123860109 | Common:2; Rare:61 | ||||
| chrX:123860116-123860454 | Common:1; Rare:75 | ||||
| chrX:123961264-123961435 | Common:2; Rare:22 |