| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109691151-109691322 | Common:3; Rare:43; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110415542-110415663 | Rare:27 | ||||
| chr6:110874616-110874796 | Common:4; Rare:61 | ||||
| chr6:110958629-110958781 | Common:2; Rare:60 | ||||
| chr6:110981950-110982109 | Common:2; Rare:81 | ||||
| chr6:111483236-111483544 | Common:1; Rare:108 | ||||
| chr6:111605830-111606104 | Common:2; Rare:50 | ||||
| chr6:112087443-112087703 | Rare:76 | ||||
| chr6:116100694-116100886 | Rare:70 | ||||
| chr6:116254062-116254222 | Common:4; Rare:43 | ||||
| chr6:116279864-116280108 | Common:2; Rare:80 | ||||
| chr6:116571196-116571627 | Common:3; Rare:123 | ||||
| chr6:116616268-116616549 | Common:3; Rare:61; Clinvar:1 | ||||
| chr6:118893913-118894313 | Common:3; Rare:122 | ||||
| chr6:119349759-119349936 | Common:2; Rare:63 |