| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:118345859-118346165 | Common:3; Rare:52 | ||||
| chrX:118495777-118495960 | Rare:33 | ||||
| chrX:118974497-118974644 | Rare:26 | ||||
| chrX:119468205-119468501 | Common:3; Rare:98 | ||||
| chrX:119574364-119574592 | Rare:51 | ||||
| chrX:119605876-119606079 | Rare:35 | ||||
| chrX:119791577-119791978 | Common:2; Rare:108 | ||||
| chrX:119852924-119853272 | Common:3; Rare:57; Clinvar (benign):3 | ||||
| chrX:119871687-119871927 | Common:1; Rare:58; Clinvar (benign):3 | ||||
| chrX:119943263-119943295 | Common:1; Rare:8 | ||||
| chrX:120560726-120560860 | Rare:20 | ||||
| chrX:120561421-120561715 | Common:1; Rare:42 | ||||
| chrX:120629938-120630261 | Common:4; Rare:64 | ||||
| chrX:123733018-123733157 | Rare:22 | ||||
| chrX:123859690-123860114 | Common:2; Rare:62 |