| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:134641551-134641849 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:134641966-134642286 | Common:5; Rare:86; Clinvar:8; Clinvar (benign):8 | ||||
| chr9:136410609-136410666 | Rare:28 | ||||
| chr9:136849548-136849782 | Common:1; Rare:89 | ||||
| chr9:136977329-136977574 | Rare:50 | ||||
| chr9:137086823-137087119 | Common:1; Rare:123; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:137188541-137188738 | Common:2; Rare:98 | ||||
| chr9:137205444-137205719 | Common:1; Rare:87 | ||||
| chr9:137423141-137423245 | Rare:37 | ||||
| chr9:137618783-137619046 | Common:1; Rare:120 | ||||
| chrM:3167-3886 | |||||
| chrM:5488-5768 | |||||
| chrM:7398-7607 | |||||
| chrM:7745-8165 | |||||
| chrM:9953-10182 |