| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:41072389-41072728 | Rare:94 | ||||
| chr6:41286660-41286813 | Common:1; Rare:35 | ||||
| chr6:41723553-41723669 | Common:2; Rare:29 | ||||
| chr6:41921077-41921223 | Common:1; Rare:38 | ||||
| chr6:42217820-42217980 | Common:5; Rare:50 | ||||
| chr6:42451523-42451660 | Common:1; Rare:21 | ||||
| chr6:42564172-42564206 | Rare:8 | ||||
| chr6:42746069-42746352 | Rare:79 | ||||
| chr6:42879577-42879944 | Rare:108 | ||||
| chr6:42929101-42929834 | Common:6; Rare:239 | ||||
| chr6:42979174-42979324 | Common:3; Rare:47; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:42984307-42984635 | Rare:86 | ||||
| chr6:43013809-43014313 | Common:2; Rare:128 | ||||
| chr6:43053719-43054011 | Common:2; Rare:107; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:43059820-43059904 | Rare:27 |