| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109382371-109382624 | Common:5; Rare:99; Clinvar (benign):1 | ||||
| chr6:109440524-109440880 | Common:2; Rare:130 | ||||
| chr6:109455589-109455835 | Common:3; Rare:61 | ||||
| chr6:109483116-109483276 | Rare:71 | ||||
| chr6:109690519-109690630 | Common:2; Rare:29 | ||||
| chr6:109691029-109691384 | Common:4; Rare:86; Clinvar:5; Clinvar (benign):3 | ||||
| chr6:110179872-110180179 | Common:2; Rare:84 | ||||
| chr6:110815108-110815280 | Common:1; Rare:61 | ||||
| chr6:110815850-110816106 | Common:2; Rare:61 | ||||
| chr6:110874659-110874796 | Common:4; Rare:40 | ||||
| chr6:110958428-110958936 | Common:11; Rare:174 | ||||
| chr6:110981954-110982109 | Common:2; Rare:79 | ||||
| chr6:111483139-111483653 | Common:1; Rare:184 | ||||
| chr6:111483707-111483779 | Common:1; Rare:32 | ||||
| chr6:111483792-111483902 | Rare:49 |