| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:78104865-78105044 | Common:2; Rare:38 | ||||
| chrX:89539302-89539415 | Common:1; Rare:22 | ||||
| chrX:96465857-96465969 | Rare:15 | ||||
| chrX:102769083-102769217 | Common:2; Rare:17 | ||||
| chrX:103404703-103404846 | Common:1; Rare:23 | ||||
| chrX:109732393-109732438 | Rare:6 | ||||
| chrX:118282035-118282211 | Common:5; Rare:33 | ||||
| chrX:119606407-119606533 | Rare:23 | ||||
| chrX:126065512-126065682 | Common:3; Rare:31 | ||||
| chrX:131830571-131830809 | Rare:37 | ||||
| chrX:135521623-135521942 | Common:3; Rare:37 | ||||
| chrX:135893348-135893728 | Common:1; Rare:77 | ||||
| chrX:151538566-151538668 | Common:2; Rare:9 | ||||
| chrX:154366134-154366370 | Common:3; Rare:71; Clinvar:7; Clinvar (benign):9 | ||||
| chrX:154368886-154369150 | Rare:47 |