| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:95577398-95577543 | Common:3; Rare:38 | ||||
| chr6:96521674-96521867 | Common:8; Rare:94 | ||||
| chr6:96897817-96898061 | Common:4; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:97283187-97283391 | Common:3; Rare:59 | ||||
| chr6:98947868-98948207 | Rare:89 | ||||
| chr6:99425245-99425448 | Common:2; Rare:56 | ||||
| chr6:100881261-100881498 | Common:5; Rare:96 | ||||
| chr6:104859837-104859998 | Common:1; Rare:51 | ||||
| chr6:106325586-106325873 | Common:1; Rare:101 | ||||
| chr6:106629270-106629363 | Common:3; Rare:24 | ||||
| chr6:106629462-106629661 | Common:3; Rare:47 | ||||
| chr6:106630041-106630355 | Common:1; Rare:63 | ||||
| chr6:106974585-106975042 | Common:5; Rare:106 | ||||
| chr6:106975312-106975526 | Common:1; Rare:62 | ||||
| chr6:107459510-107459708 | Common:1; Rare:47; Clinvar:1 |