| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:96897805-96898012 | Common:2; Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:99425259-99425486 | Common:2; Rare:65 | ||||
| chr6:100881261-100881495 | Common:5; Rare:96 | ||||
| chr6:105137081-105137264 | Common:1; Rare:70 | ||||
| chr6:106325551-106325906 | Common:1; Rare:118 | ||||
| chr6:106629442-106629588 | Common:1; Rare:30 | ||||
| chr6:108074653-108074881 | Common:1; Rare:79; Clinvar:1 | ||||
| chr6:108260915-108261284 | Common:2; Rare:149 | ||||
| chr6:109382217-109382286 | Rare:29 | ||||
| chr6:109382371-109382838 | Common:6; Rare:153; Clinvar (benign):1 | ||||
| chr6:109455706-109456035 | Common:2; Rare:86 | ||||
| chr6:109483132-109483219 | Rare:43 | ||||
| chr6:109691167-109691329 | Common:3; Rare:38; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110958225-110958575 | Common:5; Rare:73 | ||||
| chr6:110958613-110958788 | Common:4; Rare:68 |