| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:24054888-24054992 | Rare:39 | ||||
| chrX:24149623-24149744 | Rare:23 | ||||
| chrX:24465034-24465347 | Common:4; Rare:89 | ||||
| chrX:24647088-24647439 | Common:2; Rare:48 | ||||
| chrX:24693677-24693956 | Common:1; Rare:47 | ||||
| chrX:30653176-30653529 | Common:2; Rare:94 | ||||
| chrX:37847517-37847677 | Common:1; Rare:40 | ||||
| chrX:38327483-38327682 | Rare:52 | ||||
| chrX:38561313-38561577 | Common:3; Rare:63; Clinvar (benign):1 | ||||
| chrX:38801295-38801490 | Common:1; Rare:33 | ||||
| chrX:40580716-40581052 | Common:5; Rare:77; Clinvar (benign):3 | ||||
| chrX:40647525-40647770 | Common:4; Rare:81 | ||||
| chrX:40735798-40735948 | Common:1; Rare:35 | ||||
| chrX:41085219-41085491 | Common:3; Rare:79 | ||||
| chrX:41085711-41086000 | Common:1; Rare:68 |