| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120561411-120561734 | Common:1; Rare:51 | ||||
| chrX:120604061-120604154 | Rare:23 | ||||
| chrX:120629930-120630369 | Common:5; Rare:90 | ||||
| chrX:123733005-123733156 | Rare:24; Clinvar (benign):1 | ||||
| chrX:123961264-123961432 | Common:2; Rare:22 | ||||
| chrX:123961540-123961860 | Rare:46 | ||||
| chrX:129540147-129540383 | Common:3; Rare:45 | ||||
| chrX:129738941-129739216 | Common:2; Rare:47 | ||||
| chrX:129779833-129780002 | Rare:28 | ||||
| chrX:129905957-129906201 | Rare:64 | ||||
| chrX:129982318-129982586 | Rare:35 | ||||
| chrX:130165688-130165927 | Rare:46; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:132023162-132023345 | Rare:44 | ||||
| chrX:132218030-132218299 | Rare:31 | ||||
| chrX:132219427-132219514 | Rare:6 |