| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:19650374-19650594 | Common:1; Rare:28 | ||||
| chrX:19683070-19683279 | Rare:34 | ||||
| chrX:20176293-20176452 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:23786098-23786372 | Common:1; Rare:34 | ||||
| chrX:24075122-24075183 | Rare:7 | ||||
| chrX:24076456-24076695 | Common:3; Rare:28 | ||||
| chrX:29660027-29660212 | Common:4; Rare:27 | ||||
| chrX:40097955-40098107 | Rare:15 | ||||
| chrX:43176804-43176999 | Common:1; Rare:33 | ||||
| chrX:45505289-45505417 | Common:1; Rare:13 | ||||
| chrX:45512568-45512896 | Common:2; Rare:41 | ||||
| chrX:45717019-45717143 | Rare:20 | ||||
| chrX:45719916-45720077 | Common:1; Rare:22 | ||||
| chrX:45730582-45731125 | Common:3; Rare:64 | ||||
| chrX:45731467-45731860 | Common:1; Rare:40 |