| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106098702-106099006 | Rare:57 | ||||
| chr6:106325415-106325569 | Common:1; Rare:27 | ||||
| chr6:106325573-106325892 | Common:1; Rare:108 | ||||
| chr6:106629426-106629695 | Common:5; Rare:71 | ||||
| chr6:106973851-106974063 | Common:1; Rare:29 | ||||
| chr6:106975177-106975531 | Common:2; Rare:101 | ||||
| chr6:107459425-107459700 | Common:1; Rare:66; Clinvar:1 | ||||
| chr6:107490444-107490608 | Common:2; Rare:60 | ||||
| chr6:107958039-107958427 | Common:2; Rare:121; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108074647-108074846 | Rare:67; Clinvar:1 | ||||
| chr6:108260760-108261134 | Rare:148 | ||||
| chr6:108294798-108295158 | Common:2; Rare:119 | ||||
| chr6:108560726-108560917 | Rare:86 | ||||
| chr6:108656011-108656309 | Common:2; Rare:59 | ||||
| chr6:108848286-108848496 | Rare:78 |