| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:134690755-134691103 | Common:1; Rare:109; Clinvar:7; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr9:134811329-134811599 | Rare:82; Clinvar:7; Clinvar (benign):5 | ||||
| chr9:136847844-136848057 | Rare:50 | ||||
| chr9:137129722-137129811 | Common:1; Rare:29 | ||||
| chrM:221-630 | |||||
| chrM:633-1393 | |||||
| chrM:1531-1635 | |||||
| chrM:12913-13428 | |||||
| chrM:15866-15888 | |||||
| chrM:15911-15967 | |||||
| chrX:2609154-2609444 | Common:1; Rare:93 | ||||
| chrX:2707466-2707658 | Common:1; Rare:36 | ||||
| chrX:3330348-3330687 | Rare:58 | ||||
| chrX:3345883-3346061 | Rare:25 | ||||
| chrX:3526223-3526320 | Common:1; Rare:17 |