| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:109536930-109537290 | Common:5; Rare:135 | ||||
| chrX:109732882-109733573 | Common:2; Rare:202 | ||||
| chrX:110002340-110002723 | Rare:104 | ||||
| chrX:110002848-110003139 | Common:2; Rare:58 | ||||
| chrX:110318016-110318444 | Rare:159 | ||||
| chrX:111681053-111681326 | Rare:117; Clinvar (benign):14 | ||||
| chrX:111681480-111681810 | Common:1; Rare:173 | ||||
| chrX:115560500-115560910 | Common:3; Rare:93 | ||||
| chrX:115560987-115561245 | Common:2; Rare:75 | ||||
| chrX:116462855-116463175 | Rare:86 | ||||
| chrX:118116693-118116979 | Common:2; Rare:89 | ||||
| chrX:118345842-118346535 | Common:8; Rare:179 | ||||
| chrX:118727267-118727673 | Common:6; Rare:168 | ||||
| chrX:118975085-118975427 | Common:2; Rare:128 | ||||
| chrX:119236082-119236364 | Rare:76 |