| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2245430-2245846 | Common:1; Rare:140 | ||||
| chr6:2841846-2842157 | Common:3; Rare:55 | ||||
| chr6:2971524-2971674 | Common:1; Rare:42 | ||||
| chr6:2999535-3000006 | Common:11; Rare:101 | ||||
| chr6:3118581-3118755 | Common:2; Rare:59 | ||||
| chr6:3258825-3259064 | Rare:94 | ||||
| chr6:4021218-4021435 | Rare:98 | ||||
| chr6:5003646-5003843 | Common:5; Rare:62 | ||||
| chr6:5004007-5004112 | Common:1; Rare:51 | ||||
| chr6:5260681-5261025 | Common:3; Rare:116; Clinvar (benign):4 | ||||
| chr6:5261238-5261559 | Common:9; Rare:82 | ||||
| chr6:7107517-7107838 | Rare:104 | ||||
| chr6:7313139-7313383 | Common:4; Rare:83 | ||||
| chr6:7389748-7389969 | Common:1; Rare:56 | ||||
| chr6:7541405-7541678 | Rare:84; Clinvar (benign):1 |