| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103536077-103536370 | Common:1; Rare:28 | ||||
| chrX:103608784-103609089 | Common:2; Rare:48 | ||||
| chrX:107674750-107675040 | Rare:38 | ||||
| chrX:107676936-107677165 | Rare:28 | ||||
| chrX:110012873-110012955 | Common:1; Rare:5 | ||||
| chrX:114059022-114059342 | Rare:65 | ||||
| chrX:115950421-115950536 | Common:5; Rare:24 | ||||
| chrX:119552598-119552756 | Common:1; Rare:23 | ||||
| chrX:123514412-123514641 | Common:2; Rare:36 | ||||
| chrX:130138624-130138834 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chrX:135032934-135033055 | Rare:15 | ||||
| chrX:136030386-136030614 | Common:1; Rare:33 | ||||
| chrX:136055731-136056008 | Common:1; Rare:24 | ||||
| chrX:136909295-136909456 | Rare:45 | ||||
| chrX:139932160-139932452 | Common:1; Rare:56 |