| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103776553-103776882 | Common:2; Rare:32 | ||||
| chrX:104112386-104112562 | Rare:42 | ||||
| chrX:104156894-104157063 | Common:1; Rare:28 | ||||
| chrX:104566113-104566283 | Common:1; Rare:31 | ||||
| chrX:106726608-106726709 | Rare:27 | ||||
| chrX:107118571-107118899 | Common:3; Rare:61 | ||||
| chrX:107206287-107206622 | Common:2; Rare:63 | ||||
| chrX:107628268-107628517 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chrX:107716419-107716578 | Common:1; Rare:24 | ||||
| chrX:108091499-108091818 | Rare:86 | ||||
| chrX:108439453-108439883 | Common:3; Rare:97 | ||||
| chrX:108736313-108736538 | Rare:36 | ||||
| chrX:109537065-109537225 | Common:1; Rare:35 | ||||
| chrX:109733171-109733502 | Common:1; Rare:79 | ||||
| chrX:110317946-110318271 | Rare:86 |