| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143843232-143843469 | Common:2; Rare:82 | ||||
| chr6:144064561-144064604 | Rare:13 | ||||
| chr6:144095501-144095840 | Common:6; Rare:101 | ||||
| chr6:144286115-144286554 | Common:6; Rare:82 | ||||
| chr6:145814664-145814958 | Common:1; Rare:135 | ||||
| chr6:145964225-145964553 | Common:1; Rare:104 | ||||
| chr6:149545994-149546191 | Common:1; Rare:85 | ||||
| chr6:149717665-149717771 | Rare:34 | ||||
| chr6:149718066-149718385 | Common:5; Rare:89 | ||||
| chr6:149749636-149749796 | Rare:89 | ||||
| chr6:151240213-151240421 | Common:2; Rare:53 | ||||
| chr6:151452019-151452578 | Common:5; Rare:202; Clinvar (benign):3 | ||||
| chr6:152983027-152983260 | Common:2; Rare:74 | ||||
| chr6:152983452-152983759 | Common:4; Rare:105 | ||||
| chr6:153002599-153002870 | Common:4; Rare:103 |