| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47482578-47482665 | Common:5; Rare:19; Clinvar:2 | ||||
| chrX:47483169-47483241 | Common:1; Rare:10 | ||||
| chrX:47658719-47658908 | Rare:35 | ||||
| chrX:47658978-47659273 | Rare:75 | ||||
| chrX:47836791-47836953 | Common:1; Rare:38 | ||||
| chrX:48475874-48476256 | Rare:66 | ||||
| chrX:48508880-48509036 | Rare:30 | ||||
| chrX:48574211-48574549 | Common:2; Rare:94 | ||||
| chrX:48574853-48574967 | Rare:32 | ||||
| chrX:48801736-48802239 | Common:1; Rare:72 | ||||
| chrX:48911626-48911705 | Rare:17; Clinvar (benign):3 | ||||
| chrX:48958317-48958671 | Rare:74 | ||||
| chrX:49079854-49079948 | Rare:15 | ||||
| chrX:49171742-49172038 | Common:4; Rare:40 | ||||
| chrX:50814053-50814397 | Rare:74 |