| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119791590-119791978 | Common:2; Rare:102 | ||||
| chrX:119871603-119872013 | Common:3; Rare:83; Clinvar (benign):4 | ||||
| chrX:120560347-120560863 | Rare:90; Clinvar:2 | ||||
| chrX:120603796-120604152 | Rare:67 | ||||
| chrX:120629938-120630266 | Common:4; Rare:64 | ||||
| chrX:123733000-123733132 | Rare:23; Clinvar (benign):1 | ||||
| chrX:123961264-123961432 | Common:2; Rare:22 | ||||
| chrX:123961548-123961795 | Rare:36 | ||||
| chrX:129905928-129906212 | Rare:73 | ||||
| chrX:129982327-129982643 | Common:1; Rare:45 | ||||
| chrX:130165642-130165918 | Rare:55; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:132218101-132218287 | Rare:24 | ||||
| chrX:135032283-135032390 | Rare:30 | ||||
| chrX:135344545-135344823 | Common:2; Rare:48 | ||||
| chrX:135973683-135973879 | Rare:66 |