| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:99425242-99425528 | Common:2; Rare:78 | ||||
| chr6:100881160-100881506 | Common:6; Rare:125 | ||||
| chr6:106086223-106086381 | Rare:37 | ||||
| chr6:106325415-106325518 | Common:1; Rare:15 | ||||
| chr6:106325551-106325569 | Rare:3 | ||||
| chr6:106325605-106325892 | Common:1; Rare:101 | ||||
| chr6:106629466-106629649 | Common:3; Rare:43 | ||||
| chr6:106975312-106975455 | Rare:41 | ||||
| chr6:108294674-108295070 | Common:1; Rare:99 | ||||
| chr6:108560726-108560913 | Rare:85 | ||||
| chr6:109382208-109382328 | Rare:53 | ||||
| chr6:109382348-109382863 | Common:7; Rare:172; Clinvar (benign):1 | ||||
| chr6:109440567-109440866 | Common:2; Rare:106 | ||||
| chr6:109691151-109691322 | Common:3; Rare:43; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179623-110179663 | Rare:12 |