| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:19343701-19344040 | Common:6; Rare:95; Clinvar (benign):1 | ||||
| chrX:20267009-20267281 | Common:1; Rare:48 | ||||
| chrX:21658249-21658536 | Common:1; Rare:59 | ||||
| chrX:23782913-23783319 | Common:5; Rare:86 | ||||
| chrX:23783346-23783717 | Common:3; Rare:81 | ||||
| chrX:23785321-23785560 | Common:1; Rare:44 | ||||
| chrX:23907716-23907792 | Rare:17 | ||||
| chrX:23907873-23908136 | Rare:57 | ||||
| chrX:24054908-24054971 | Rare:19 | ||||
| chrX:24149594-24149786 | Rare:33 | ||||
| chrX:24465241-24465355 | Common:3; Rare:35 | ||||
| chrX:37685650-37685852 | Common:1; Rare:32 | ||||
| chrX:41085221-41085483 | Common:3; Rare:76 | ||||
| chrX:41085572-41085877 | Rare:65 | ||||
| chrX:43656127-43656433 | Rare:56 |