| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119399017-119399333 | Common:2; Rare:58 | ||||
| chrX:119468204-119468506 | Common:3; Rare:99 | ||||
| chrX:119469058-119469260 | Rare:57 | ||||
| chrX:119574333-119574645 | Rare:62 | ||||
| chrX:119791611-119791994 | Common:2; Rare:95 | ||||
| chrX:119871648-119872007 | Common:2; Rare:76; Clinvar (benign):4 | ||||
| chrX:119943221-119943302 | Common:1; Rare:18 | ||||
| chrX:119943595-119943852 | Rare:45 | ||||
| chrX:120469096-120469366 | Common:1; Rare:61; Clinvar:9; Clinvar (benign):5 | ||||
| chrX:120538489-120538768 | Rare:34 | ||||
| chrX:120559823-120560139 | Rare:49 | ||||
| chrX:120560650-120560878 | Rare:38 | ||||
| chrX:120561376-120561636 | Common:1; Rare:43 | ||||
| chrX:120603983-120604350 | Rare:62 | ||||
| chrX:120604587-120604870 | Rare:34 |