| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42781761-42782060 | Common:12; Rare:67 | ||||
| chr6:42984302-42984592 | Rare:70 | ||||
| chr6:43013908-43014270 | Common:1; Rare:74 | ||||
| chr6:43516887-43517102 | Common:3; Rare:83; Clinvar:2 | ||||
| chr6:43770070-43770221 | Common:2; Rare:45 | ||||
| chr6:44127395-44127669 | Common:4; Rare:74 | ||||
| chr6:44246880-44247192 | Common:4; Rare:131 | ||||
| chr6:46652816-46653022 | Rare:47 | ||||
| chr6:49463166-49463401 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:50818691-50818919 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:52420085-52420349 | Common:3; Rare:114; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52995273-52995829 | Common:4; Rare:227 | ||||
| chr6:56247526-56247680 | Common:2; Rare:27 | ||||
| chr6:57046442-57046729 | Rare:102 | ||||
| chr6:62286151-62286352 | Rare:58 |