| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106629462-106629624 | Common:1; Rare:34 | ||||
| chr6:107459517-107459637 | Common:1; Rare:31; Clinvar:1 | ||||
| chr6:107490451-107490590 | Common:2; Rare:50 | ||||
| chr6:108074659-108074838 | Rare:57; Clinvar:1 | ||||
| chr6:108165857-108166092 | Rare:47 | ||||
| chr6:108260912-108261085 | Rare:85 | ||||
| chr6:108294782-108295070 | Common:1; Rare:77 | ||||
| chr6:108848190-108848496 | Common:1; Rare:102 | ||||
| chr6:109382377-109382577 | Common:4; Rare:85; Clinvar (benign):1 | ||||
| chr6:109440532-109440856 | Common:1; Rare:116 | ||||
| chr6:109455726-109456093 | Common:2; Rare:85 | ||||
| chr6:109483132-109483276 | Rare:63 | ||||
| chr6:109691145-109691322 | Common:3; Rare:46; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110958466-110958815 | Common:7; Rare:124 | ||||
| chr6:110981959-110982100 | Common:2; Rare:68 |