| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:5708272-5708805 | Common:10; Rare:361; Clinvar:6; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr4:5710890-5711610 | Common:1; Rare:470; Clinvar:13; Clinvar (benign):5 | ||||
| chr4:6200453-6200853 | Common:5; Rare:305 | ||||
| chr4:6574851-6575331 | Common:19; Rare:681 | ||||
| chr4:6639852-6640257 | Common:10; Rare:147 | ||||
| chr4:6640359-6641156 | Common:25; Rare:974 | ||||
| chr4:6692700-6693100 | Common:8; Rare:119 | ||||
| chr4:6693014-6693941 | Common:5; Rare:505 | ||||
| chr4:6709428-6710158 | Common:13; Rare:742 | ||||
| chr4:6715214-6715699 | Common:4; Rare:144 | ||||
| chr4:6715839-6716245 | Common:5; Rare:560 | ||||
| chr4:6716329-6716774 | Common:2; Rare:246 | ||||
| chr4:6781992-6782392 | Common:3; Rare:122 | ||||
| chr4:6782424-6782834 | Common:11; Rare:674 | ||||
| chr4:6909107-6910863 | Common:12; Rare:1832 |