| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:137188547-137188744 | Common:2; Rare:98 | ||||
| chr9:137205457-137205733 | Common:1; Rare:87 | ||||
| chr9:137550382-137550477 | Rare:13 | ||||
| chr9:137618824-137619043 | Common:1; Rare:97 | ||||
| chrM:4319-4360 | |||||
| chrX:2691423-2691507 | Common:1; Rare:50 | ||||
| chrX:7927361-7927474 | Common:1; Rare:31 | ||||
| chrX:7927695-7927778 | Rare:17 | ||||
| chrX:11111175-11111474 | Common:4; Rare:52 | ||||
| chrX:12975005-12975166 | Common:1; Rare:40 | ||||
| chrX:13734576-13734849 | Common:3; Rare:83; Clinvar (benign):1 | ||||
| chrX:14873192-14873470 | Rare:48 | ||||
| chrX:18984034-18984229 | Rare:46 | ||||
| chrX:20141757-20142062 | Common:1; Rare:68 | ||||
| chrX:21658378-21658529 | Rare:34 |