| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:101407793-101408287 | Common:10; Rare:174; Clinvar:4; Clinvar (benign):22 | ||||
| chrX:101622832-101623209 | Common:2; Rare:57 | ||||
| chrX:103064155-103064308 | Common:2; Rare:28 | ||||
| chrX:103255108-103255222 | Rare:14 | ||||
| chrX:103356341-103356556 | Common:4; Rare:56 | ||||
| chrX:103628964-103629658 | Common:2; Rare:302 | ||||
| chrX:103686643-103686973 | Common:4; Rare:88 | ||||
| chrX:103687092-103687351 | Common:1; Rare:49 | ||||
| chrX:103918744-103918897 | Common:2; Rare:40 | ||||
| chrX:103919039-103919197 | Common:4; Rare:33 | ||||
| chrX:104112265-104112665 | Rare:113 | ||||
| chrX:104156923-104157089 | Common:2; Rare:61 | ||||
| chrX:104166205-104166575 | Common:1; Rare:80 | ||||
| chrX:106038689-106039003 | Common:2; Rare:90 | ||||
| chrX:106693420-106693850 | Common:2; Rare:86 |