| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:107206275-107206665 | Common:2; Rare:76 | ||||
| chrX:107628267-107628531 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chrX:107716309-107716817 | Common:1; Rare:81 | ||||
| chrX:107716844-107717089 | Common:2; Rare:30 | ||||
| chrX:107775573-107775871 | Rare:50 | ||||
| chrX:107775877-107775988 | Common:1; Rare:15 | ||||
| chrX:107775993-107776116 | Common:3; Rare:26 | ||||
| chrX:107825680-107825887 | Common:1; Rare:28 | ||||
| chrX:108091428-108091819 | Rare:101 | ||||
| chrX:108439502-108439853 | Common:2; Rare:82 | ||||
| chrX:109537065-109537237 | Common:1; Rare:36 | ||||
| chrX:109733150-109733500 | Common:1; Rare:82 | ||||
| chrX:110002252-110002452 | Common:1; Rare:29 | ||||
| chrX:110317902-110318248 | Rare:90 | ||||
| chrX:111095992-111096191 | Rare:29 |