| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:2813006-2813195 | Common:2; Rare:30 | ||||
| chr4:2832652-2832820 | Common:1; Rare:46 | ||||
| chr4:2835204-2835454 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:2845387-2845558 | Rare:29 | ||||
| chr4:2936177-2936274 | Rare:17 | ||||
| chr4:3013909-3014107 | Common:1; Rare:38 | ||||
| chr4:3040054-3040360 | Common:1; Rare:56 | ||||
| chr4:3040506-3040658 | Common:1; Rare:49 | ||||
| chr4:3041209-3041708 | Common:5; Rare:112 | ||||
| chr4:3041730-3042102 | Common:4; Rare:87 | ||||
| chr4:3042116-3042158 | Rare:20 | ||||
| chr4:3042423-3042489 | Rare:8 | ||||
| chr4:3047840-3048094 | Common:2; Rare:54 | ||||
| chr4:3075185-3075775 | Common:8; Rare:142 | ||||
| chr4:3076706-3076897 | Rare:36 |