| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:108439455-108439863 | Common:2; Rare:95 | ||||
| chrX:109733171-109733480 | Common:1; Rare:73 | ||||
| chrX:110318077-110318248 | Rare:41 | ||||
| chrX:112840822-112841004 | Rare:39 | ||||
| chrX:115561004-115561243 | Common:1; Rare:42 | ||||
| chrX:116436442-116436693 | Rare:33 | ||||
| chrX:118345861-118346165 | Common:3; Rare:51 | ||||
| chrX:119236538-119236667 | Rare:37 | ||||
| chrX:119468205-119468496 | Common:3; Rare:97 | ||||
| chrX:119574367-119574586 | Rare:49 | ||||
| chrX:119574811-119574910 | Common:2; Rare:17 | ||||
| chrX:119791584-119791994 | Common:2; Rare:111 | ||||
| chrX:119871638-119871962 | Common:1; Rare:69; Clinvar (benign):3 | ||||
| chrX:120560480-120560860 | Rare:60; Clinvar:2 | ||||
| chrX:120629912-120630356 | Common:5; Rare:88 |