| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103586435-103586744 | Rare:67 | ||||
| chrX:103607869-103608140 | Rare:43 | ||||
| chrX:103628533-103629003 | Common:3; Rare:60 | ||||
| chrX:103629448-103629545 | Rare:24 | ||||
| chrX:103686685-103687029 | Common:4; Rare:46 | ||||
| chrX:103687225-103687275 | Rare:11 | ||||
| chrX:103687989-103688127 | Rare:28 | ||||
| chrX:104156894-104157063 | Common:1; Rare:28 | ||||
| chrX:107628359-107628523 | Common:1; Rare:20; Clinvar (benign):1 | ||||
| chrX:107716688-107716890 | Rare:43 | ||||
| chrX:107716904-107717181 | Common:2; Rare:35 | ||||
| chrX:107775582-107775874 | Rare:49 | ||||
| chrX:107775907-107775988 | Common:1; Rare:12 | ||||
| chrX:107825471-107825751 | Common:2; Rare:25 | ||||
| chrX:108091504-108091818 | Rare:85 |