| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:106802537-106802778 | Rare:49 | ||||
| chrX:107118777-107118889 | Common:2; Rare:23 | ||||
| chrX:108091513-108091822 | Rare:81 | ||||
| chrX:108439479-108439901 | Common:3; Rare:93 | ||||
| chrX:109733158-109733502 | Common:1; Rare:82 | ||||
| chrX:110317886-110318294 | Rare:109 | ||||
| chrX:115561017-115561251 | Common:1; Rare:40 | ||||
| chrX:118116767-118116933 | Common:1; Rare:25 | ||||
| chrX:118345818-118346171 | Common:4; Rare:64 | ||||
| chrX:119236551-119236618 | Rare:20 | ||||
| chrX:119468205-119468506 | Common:3; Rare:99 | ||||
| chrX:119574373-119574639 | Rare:55 | ||||
| chrX:119791581-119791978 | Common:2; Rare:107 | ||||
| chrX:119852932-119853276 | Common:3; Rare:56; Clinvar (benign):3 | ||||
| chrX:119871622-119871923 | Common:2; Rare:61; Clinvar (benign):3 |