| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:108560726-108560879 | Rare:69 | ||||
| chr6:108848325-108848475 | Rare:56 | ||||
| chr6:109009450-109009677 | Common:2; Rare:73 | ||||
| chr6:109382392-109382566 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chr6:109440562-109440728 | Rare:59 | ||||
| chr6:109455702-109455823 | Common:1; Rare:34 | ||||
| chr6:109691158-109691339 | Common:3; Rare:42; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110874626-110874810 | Common:4; Rare:60 | ||||
| chr6:110958566-110958764 | Common:4; Rare:66 | ||||
| chr6:111483154-111483393 | Common:1; Rare:74 | ||||
| chr6:111605535-111605606 | Rare:14 | ||||
| chr6:111605950-111605975 | Rare:9 | ||||
| chr6:111759901-111760149 | Common:3; Rare:52 | ||||
| chr6:111793870-111794036 | Rare:39 | ||||
| chr6:112087261-112087663 | Common:1; Rare:141 |