| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:100881287-100881482 | Common:5; Rare:86 | ||||
| chr6:106325619-106325872 | Common:1; Rare:89 | ||||
| chr6:106629451-106629595 | Common:1; Rare:28 | ||||
| chr6:107459555-107459723 | Common:1; Rare:38 | ||||
| chr6:108074676-108074955 | Common:1; Rare:93; Clinvar:1 | ||||
| chr6:108260927-108261118 | Rare:88 | ||||
| chr6:109455726-109455842 | Rare:26 | ||||
| chr6:109691167-109691315 | Common:1; Rare:36; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:112087463-112087678 | Rare:60 | ||||
| chr6:116254068-116254171 | Common:1; Rare:21 | ||||
| chr6:116279903-116280038 | Rare:41 | ||||
| chr6:116571175-116571593 | Common:3; Rare:121 | ||||
| chr6:117602471-117602683 | Common:3; Rare:58 | ||||
| chr6:118893885-118894205 | Common:3; Rare:98 | ||||
| chr6:122471773-122471917 | Common:2; Rare:41 |