| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:110944272-110944610 | Rare:42 | ||||
| chrX:111095992-111096399 | Common:1; Rare:58 | ||||
| chrX:111410141-111410704 | Rare:64; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chrX:111410773-111411084 | Rare:59; Clinvar (pathogenic):1 | ||||
| chrX:111411673-111411862 | Common:1; Rare:23 | ||||
| chrX:111411986-111412317 | Rare:39 | ||||
| chrX:111681031-111681302 | Rare:70; Clinvar (benign):7 | ||||
| chrX:111681536-111681673 | Rare:50 | ||||
| chrX:112082894-112082990 | Common:1; Rare:23 | ||||
| chrX:112840815-112841075 | Rare:54 | ||||
| chrX:114583901-114584092 | Common:2; Rare:33; Clinvar:1 | ||||
| chrX:117973207-117973285 | Rare:10 | ||||
| chrX:118345859-118346204 | Common:4; Rare:61 | ||||
| chrX:118346471-118346506 | Rare:12 | ||||
| chrX:118823648-118823855 | Rare:52 |