| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:45377793-45378198 | Common:2; Rare:132 | ||||
| chr6:46129760-46130180 | Common:5; Rare:130 | ||||
| chr6:46325586-46325823 | Common:1; Rare:36 | ||||
| chr6:46491920-46492029 | Rare:22 | ||||
| chr6:46652816-46653013 | Rare:46 | ||||
| chr6:47309862-47309989 | Common:1; Rare:24 | ||||
| chr6:47477589-47478089 | Common:4; Rare:131; Clinvar:5; Clinvar (benign):5 | ||||
| chr6:48068138-48068175 | Rare:5 | ||||
| chr6:48068444-48068932 | Common:4; Rare:165 | ||||
| chr6:49463138-49463401 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:52284705-52285006 | Common:2; Rare:102 | ||||
| chr6:52420122-52420413 | Common:3; Rare:119; Clinvar:1; Clinvar (benign):3 | ||||
| chr6:52671028-52671236 | Rare:52 | ||||
| chr6:52994231-52994291 | Rare:17 | ||||
| chr6:52995259-52995807 | Common:4; Rare:228 |