| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:10813-11277 | |||||
| chrM:11861-12138 | |||||
| chrM:14532-14972 | |||||
| chrX:1392053-1392394 | Common:6; Rare:149 | ||||
| chrX:2929277-2929513 | Common:2; Rare:68 | ||||
| chrX:7927365-7927474 | Common:1; Rare:31 | ||||
| chrX:7927695-7927799 | Rare:24 | ||||
| chrX:11111136-11111368 | Common:3; Rare:50 | ||||
| chrX:12975005-12975168 | Common:2; Rare:40 | ||||
| chrX:13734537-13734832 | Common:3; Rare:91; Clinvar (benign):1 | ||||
| chrX:13735011-13735153 | Rare:39; Clinvar (benign):1 | ||||
| chrX:14029578-14029697 | Rare:14 | ||||
| chrX:14029800-14030029 | Common:2; Rare:69 | ||||
| chrX:14873034-14873463 | Common:1; Rare:80 | ||||
| chrX:15493204-15493437 | Common:1; Rare:37 |