| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:137550362-137550491 | Rare:19 | ||||
| chr9:137551589-137551977 | Common:29; Rare:166 | ||||
| chr9:137578864-137579052 | Common:2; Rare:59 | ||||
| chr9:137618797-137619035 | Common:1; Rare:107 | ||||
| chrM:4312-4332 | |||||
| chrM:4434-5390 | |||||
| chrM:5426-5744 | |||||
| chrM:7387-8172 | |||||
| chrM:9953-10182 | |||||
| chrX:1391989-1392281 | Common:6; Rare:138 | ||||
| chrX:7927371-7927468 | Common:1; Rare:29 | ||||
| chrX:7927695-7927770 | Rare:13 | ||||
| chrX:11111162-11111410 | Common:4; Rare:48 | ||||
| chrX:11427739-11427928 | Rare:42 | ||||
| chrX:13734524-13734832 | Common:3; Rare:95; Clinvar (benign):1 |