| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:85003738-85003909 | Common:2; Rare:32 | ||||
| chrX:85243818-85244154 | Common:3; Rare:66; Clinvar (benign):1 | ||||
| chrX:86047280-86047415 | Rare:19 | ||||
| chrX:86047489-86047636 | Common:1; Rare:36 | ||||
| chrX:86148245-86148461 | Common:1; Rare:41 | ||||
| chrX:91779316-91779381 | Common:1; Rare:12 | ||||
| chrX:93673546-93673790 | Common:1; Rare:40 | ||||
| chrX:101051862-101052237 | Common:2; Rare:62 | ||||
| chrX:101348684-101348753 | Common:3; Rare:13 | ||||
| chrX:101390705-101391096 | Rare:102 | ||||
| chrX:101407845-101408292 | Common:5; Rare:84; Clinvar:2; Clinvar (benign):11 | ||||
| chrX:101418006-101418290 | Common:2; Rare:46 | ||||
| chrX:101485096-101485462 | Rare:51 | ||||
| chrX:101550402-101550618 | Rare:32 | ||||
| chrX:102155866-102156090 | Common:2; Rare:24 |