| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109691163-109691322 | Common:3; Rare:38; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110958497-110958637 | Common:3; Rare:33 | ||||
| chr6:110958643-110958792 | Common:2; Rare:67 | ||||
| chr6:110981975-110982109 | Common:2; Rare:72 | ||||
| chr6:112087446-112087658 | Rare:66 | ||||
| chr6:113971112-113971494 | Common:3; Rare:119 | ||||
| chr6:116060753-116060983 | Common:1; Rare:44 | ||||
| chr6:116100709-116100895 | Common:1; Rare:68 | ||||
| chr6:116253982-116254214 | Common:5; Rare:72 | ||||
| chr6:116279413-116279652 | Common:3; Rare:86 | ||||
| chr6:116279750-116279938 | Common:1; Rare:73 | ||||
| chr6:116370691-116371060 | Common:1; Rare:87 | ||||
| chr6:116571170-116571618 | Common:3; Rare:131 | ||||
| chr6:117602451-117602660 | Common:3; Rare:60 | ||||
| chr6:117675314-117675498 | Common:3; Rare:51 |