| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:2962530-2962983 | Common:1; Rare:197 | ||||
| chr4:2963280-2963727 | Common:18; Rare:781 | ||||
| chr4:2963950-2964270 | Common:5; Rare:225 | ||||
| chr4:3073980-3074430 | Common:7; Rare:71 | ||||
| chr4:3074450-3074759 | Common:14; Rare:263 | ||||
| chr4:3292715-3293497 | Common:16; Rare:723 | ||||
| chr4:3532333-3532733 | Common:6; Rare:394 | ||||
| chr4:3765490-3765950 | Common:5; Rare:135 | ||||
| chr4:3766130-3766634 | Common:8; Rare:181 | ||||
| chr4:4247323-4247723 | Common:5; Rare:106 | ||||
| chr4:4247930-4249061 | Common:43; Rare:858 | ||||
| chr4:4289997-4290397 | Common:32; Rare:646 | ||||
| chr4:4541878-4542589 | Common:18; Rare:915 | ||||
| chr4:4859403-4860166 | Common:13; Rare:583; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr4:5051230-5051720 | Common:10; Rare:352 |