| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:100881084-100881482 | Common:7; Rare:130 | ||||
| chr6:105137031-105137316 | Common:2; Rare:98 | ||||
| chr6:106086192-106086381 | Rare:50 | ||||
| chr6:106325551-106325892 | Common:1; Rare:112 | ||||
| chr6:106629454-106629656 | Common:3; Rare:47 | ||||
| chr6:107459528-107459692 | Common:1; Rare:37 | ||||
| chr6:107490451-107490606 | Common:2; Rare:58 | ||||
| chr6:107958068-107958428 | Common:2; Rare:110; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108074647-108074919 | Common:1; Rare:97; Clinvar:1 | ||||
| chr6:108260764-108261023 | Rare:114 | ||||
| chr6:108294802-108295071 | Common:1; Rare:72 | ||||
| chr6:108560719-108560988 | Rare:111 | ||||
| chr6:108656011-108656331 | Common:2; Rare:65 | ||||
| chr6:108848286-108848496 | Rare:78 | ||||
| chr6:109009384-109009689 | Common:2; Rare:88 |