| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103585455-103585670 | Common:3; Rare:44 | ||||
| chrX:103586463-103586783 | Rare:67 | ||||
| chrX:103628922-103628974 | Rare:6 | ||||
| chrX:103628990-103629003 | Rare:3 | ||||
| chrX:104156974-104157069 | Rare:15 | ||||
| chrX:107716441-107716597 | Common:1; Rare:25 | ||||
| chrX:108091516-108091818 | Rare:80 | ||||
| chrX:108439457-108439901 | Common:3; Rare:99 | ||||
| chrX:109733171-109733570 | Common:1; Rare:91 | ||||
| chrX:110317871-110318236 | Rare:97 | ||||
| chrX:118345859-118346165 | Common:3; Rare:52 | ||||
| chrX:119574373-119574594 | Rare:50 | ||||
| chrX:119791601-119791721 | Rare:49 | ||||
| chrX:119871621-119871891 | Common:2; Rare:55; Clinvar (benign):2 | ||||
| chrX:123733015-123733071 | Rare:14 |