| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:118495733-118495856 | Rare:18 | ||||
| chrX:119236531-119236652 | Rare:37 | ||||
| chrX:119468204-119468506 | Common:3; Rare:99 | ||||
| chrX:119574356-119574575 | Rare:48 | ||||
| chrX:119791626-119791978 | Common:2; Rare:85 | ||||
| chrX:119871666-119871949 | Common:1; Rare:63; Clinvar (benign):3 | ||||
| chrX:120559884-120560131 | Rare:41 | ||||
| chrX:120560362-120560860 | Rare:83; Clinvar:2 | ||||
| chrX:120603991-120604217 | Rare:44 | ||||
| chrX:123733009-123733189 | Rare:33; Clinvar (benign):1 | ||||
| chrX:130110549-130110635 | Rare:21 | ||||
| chrX:130165654-130165937 | Rare:54; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:135344694-135344821 | Rare:23 | ||||
| chrX:141176501-141176747 | Rare:64 | ||||
| chrX:141177068-141177302 | Common:1; Rare:28 |