| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32177042-32177411 | Common:1; Rare:63 | ||||
| chr6:32178074-32178696 | Common:3; Rare:130 | ||||
| chr6:32190137-32190346 | Rare:41 | ||||
| chr6:32838219-32838345 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr6:32838681-32839130 | Common:8; Rare:71 | ||||
| chr6:32843986-32844149 | Rare:37; Clinvar:1 | ||||
| chr6:32844328-32844854 | Common:1; Rare:115 | ||||
| chr6:32853633-32854267 | Common:5; Rare:189; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:32940891-32941184 | Common:1; Rare:53 | ||||
| chr6:32968447-32968616 | Common:3; Rare:43 | ||||
| chr6:32968788-32968933 | Common:4; Rare:48 | ||||
| chr6:32970155-32970267 | Common:1; Rare:28 | ||||
| chr6:32970612-32970956 | Common:2; Rare:89 | ||||
| chr6:32977488-32977974 | Common:4; Rare:169; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:33075713-33076140 | Common:8; Rare:65 |