| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:90587049-90587357 | Common:3; Rare:78 | ||||
| chr6:96521674-96521867 | Common:8; Rare:94 | ||||
| chr6:96897810-96898012 | Common:2; Rare:79; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:99425259-99425490 | Common:2; Rare:66 | ||||
| chr6:100881285-100881439 | Common:4; Rare:65 | ||||
| chr6:106325619-106325892 | Common:1; Rare:96 | ||||
| chr6:106629474-106629600 | Common:1; Rare:23 | ||||
| chr6:109382266-109382587 | Common:5; Rare:136; Clinvar (benign):2 | ||||
| chr6:109691167-109691315 | Common:1; Rare:36; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:110958591-110958775 | Common:4; Rare:66 | ||||
| chr6:112087474-112087634 | Rare:39 | ||||
| chr6:116100718-116100882 | Rare:59 | ||||
| chr6:116571196-116571563 | Common:2; Rare:103 | ||||
| chr6:122399351-122399696 | Common:6; Rare:125 | ||||
| chr6:122471762-122471915 | Common:2; Rare:46 |