| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:12293630-12294412 | Common:3; Rare:175; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr6:12294450-12294532 | Rare:11 | ||||
| chr6:12295745-12295841 | Common:2; Rare:16 | ||||
| chr6:12301650-12301662 | Rare:2 | ||||
| chr6:12311190-12311555 | Common:1; Rare:58 | ||||
| chr6:12312861-12313066 | Common:2; Rare:31 | ||||
| chr6:12313334-12313400 | Rare:4 | ||||
| chr6:12313428-12313497 | Rare:9 | ||||
| chr6:12313700-12313809 | Rare:19 | ||||
| chr6:12314052-12314151 | Rare:19 | ||||
| chr6:12314194-12314441 | Common:1; Rare:39 | ||||
| chr6:12314903-12315018 | Common:1; Rare:16 | ||||
| chr6:12332092-12332373 | Rare:51 | ||||
| chr6:12483819-12484095 | Common:3; Rare:56 | ||||
| chr6:15245191-15245582 | Common:2; Rare:111 |