| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:8252-8541 | |||||
| chrM:9007-9357 | |||||
| chrM:9551-9678 | |||||
| chrM:10393-10508 | |||||
| chrM:12096-12138 | |||||
| chrM:15011-15183 | |||||
| chrX:1392036-1392349 | Common:6; Rare:144 | ||||
| chrX:2929271-2929513 | Common:2; Rare:68 | ||||
| chrX:7927367-7927512 | Common:1; Rare:36 | ||||
| chrX:10576886-10577008 | Rare:19 | ||||
| chrX:11111136-11111382 | Common:4; Rare:53 | ||||
| chrX:12975005-12975163 | Common:1; Rare:39 | ||||
| chrX:13734569-13734815 | Common:3; Rare:79; Clinvar (benign):1 | ||||
| chrX:14029800-14029955 | Common:1; Rare:46 | ||||
| chrX:14873031-14873534 | Common:2; Rare:98 |