| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:115561017-115561244 | Common:1; Rare:39 | ||||
| chrX:119236546-119236685 | Rare:34 | ||||
| chrX:119468205-119468456 | Common:3; Rare:70 | ||||
| chrX:119469090-119469148 | Rare:16 | ||||
| chrX:119574364-119574755 | Common:1; Rare:78 | ||||
| chrX:119791590-119791978 | Common:2; Rare:102 | ||||
| chrX:119871614-119871914 | Common:2; Rare:61; Clinvar (benign):3 | ||||
| chrX:120560501-120560859 | Rare:54; Clinvar:1 | ||||
| chrX:120561404-120561692 | Common:1; Rare:44 | ||||
| chrX:120604062-120604172 | Rare:28 | ||||
| chrX:123184315-123184374 | Rare:16 | ||||
| chrX:123733021-123733159 | Rare:22 | ||||
| chrX:123961264-123961435 | Common:2; Rare:22 | ||||
| chrX:123961533-123961860 | Rare:46 | ||||
| chrX:129779833-129779971 | Rare:21 |