| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:101052091-101052198 | Rare:15 | ||||
| chrX:101348704-101348771 | Common:2; Rare:7 | ||||
| chrX:101407841-101408261 | Common:5; Rare:79; Clinvar:2; Clinvar (benign):11 | ||||
| chrX:103376427-103376607 | Common:1; Rare:27 | ||||
| chrX:103686663-103687046 | Common:4; Rare:54 | ||||
| chrX:104156974-104157028 | Rare:6 | ||||
| chrX:108091516-108091818 | Rare:80 | ||||
| chrX:108439502-108439853 | Common:2; Rare:82 | ||||
| chrX:110318077-110318296 | Rare:58 | ||||
| chrX:111681212-111681243 | Rare:11; Clinvar (benign):1 | ||||
| chrX:115561005-115561251 | Common:1; Rare:43 | ||||
| chrX:118345859-118346171 | Common:3; Rare:55 | ||||
| chrX:119236585-119236616 | Rare:8 | ||||
| chrX:119468205-119468506 | Common:3; Rare:99 | ||||
| chrX:119574388-119574581 | Rare:42 |