| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:52420108-52420385 | Common:3; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576992-52577292 | Common:5; Rare:111 | ||||
| chr6:52671054-52671178 | Rare:35 | ||||
| chr6:52995260-52995832 | Common:4; Rare:231 | ||||
| chr6:53061687-53061935 | Rare:58 | ||||
| chr6:53065369-53065618 | Common:1; Rare:76 | ||||
| chr6:53065705-53065730 | Rare:7 | ||||
| chr6:53348847-53349076 | Common:2; Rare:110 | ||||
| chr6:53349137-53349298 | Rare:37 | ||||
| chr6:53545097-53545234 | Rare:40 | ||||
| chr6:53616583-53616787 | Common:1; Rare:33 | ||||
| chr6:56542761-56543034 | Common:2; Rare:47 | ||||
| chr6:56642364-56642735 | Common:2; Rare:95; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:56642737-56642945 | Rare:51; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:56642955-56643117 | Rare:36 |