| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:97283135-97283302 | Common:1; Rare:54 | ||||
| chr6:98947881-98948207 | Rare:87 | ||||
| chr6:99424750-99424971 | Rare:68 | ||||
| chr6:99425214-99425532 | Common:2; Rare:92 | ||||
| chr6:99425656-99425760 | Common:1; Rare:24 | ||||
| chr6:99515395-99515571 | Common:1; Rare:59 | ||||
| chr6:100464859-100465219 | Common:3; Rare:97 | ||||
| chr6:100881226-100881489 | Common:5; Rare:100 | ||||
| chr6:106325551-106325898 | Common:1; Rare:114 | ||||
| chr6:106629426-106629681 | Common:5; Rare:65 | ||||
| chr6:106975194-106975421 | Rare:63 | ||||
| chr6:107459479-107459676 | Common:1; Rare:52; Clinvar:1 | ||||
| chr6:107490433-107490617 | Common:3; Rare:66 | ||||
| chr6:107957261-107957371 | Rare:25 | ||||
| chr6:107958075-107958374 | Common:2; Rare:89; Clinvar:2; Clinvar (benign):3 |