| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:37493815-37494121 | Common:3; Rare:54 | ||||
| chr8:127794357-127794575 | Rare:56 | ||||
| chr9:35684248-35684503 | Rare:53; Clinvar:2; Clinvar (benign):4 | ||||
| chr9:62802625-62802781 | |||||
| chr9:111366282-111366528 | Common:2; Rare:57 | ||||
| chr9:136438947-136439097 | Rare:54 | ||||
| chr9:136728178-136728352 | Common:3; Rare:68 | ||||
| chrM:260-843 | |||||
| chrM:1388-1833 | |||||
| chrM:1841-2120 | |||||
| chrM:3872-3954 | |||||
| chrM:13272-13422 | |||||
| chrM:15381-15895 | |||||
| chrX:15675609-15675714 | Rare:18 |