| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106629443-106629638 | Common:3; Rare:41 | ||||
| chr6:107459485-107459676 | Common:1; Rare:49; Clinvar:1 | ||||
| chr6:107490451-107490579 | Common:2; Rare:45 | ||||
| chr6:108074647-108074866 | Common:1; Rare:77; Clinvar:1 | ||||
| chr6:108260917-108261023 | Rare:65 | ||||
| chr6:108294790-108295076 | Common:1; Rare:77 | ||||
| chr6:108560726-108560978 | Rare:104 | ||||
| chr6:108848317-108848475 | Rare:58 | ||||
| chr6:109009456-109009682 | Common:2; Rare:73 | ||||
| chr6:109095437-109095557 | Rare:23 | ||||
| chr6:109382233-109382298 | Rare:30 | ||||
| chr6:109382308-109382522 | Common:3; Rare:103; Clinvar (benign):2 | ||||
| chr6:109440575-109440872 | Common:2; Rare:104 | ||||
| chr6:109691163-109691322 | Common:3; Rare:38; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179962-110180162 | Common:2; Rare:60 |