| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:17375621-17375923 | Rare:42; Clinvar:2 | ||||
| chrX:17737166-17737624 | Common:4; Rare:49 | ||||
| chrX:17738030-17738700 | Common:2; Rare:167 | ||||
| chrX:18425346-18425655 | Common:5; Rare:138; Clinvar:2; Clinvar (benign):6 | ||||
| chrX:18984010-18984920 | Common:2; Rare:324 | ||||
| chrX:18984855-18985089 | Common:1; Rare:69 | ||||
| chrX:19343674-19344021 | Common:12; Rare:183; Clinvar (benign):2 | ||||
| chrX:19515430-19515617 | Common:2; Rare:74 | ||||
| chrX:19670337-19670790 | Common:4; Rare:83 | ||||
| chrX:19670867-19671002 | Rare:45 | ||||
| chrX:19887513-19887826 | Rare:82 | ||||
| chrX:20141800-20142083 | Common:2; Rare:108 | ||||
| chrX:20266589-20266738 | Rare:56 | ||||
| chrX:20266848-20267194 | Common:1; Rare:115 | ||||
| chrX:21839486-21839751 | Rare:119 |