| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:107206364-107206614 | Common:1; Rare:47 | ||||
| chrX:107716230-107716856 | Common:1; Rare:111 | ||||
| chrX:107775600-107775943 | Rare:59 | ||||
| chrX:108091500-108091818 | Rare:86 | ||||
| chrX:108439480-108439878 | Common:2; Rare:90 | ||||
| chrX:109733171-109733502 | Common:1; Rare:79 | ||||
| chrX:110318072-110318246 | Rare:43 | ||||
| chrX:111681535-111681710 | Rare:65 | ||||
| chrX:112840822-112841033 | Rare:44 | ||||
| chrX:118345880-118346174 | Common:3; Rare:51 | ||||
| chrX:119468238-119468506 | Common:3; Rare:93 | ||||
| chrX:119469090-119469282 | Rare:56 | ||||
| chrX:119574374-119574594 | Rare:50 | ||||
| chrX:119791590-119791700 | Rare:42 | ||||
| chrX:119871624-119871921 | Common:1; Rare:61; Clinvar (benign):3 |