| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:4542317-4542469 | Common:4; Rare:75 | ||||
| chr4:4859508-4859721 | Common:2; Rare:156 | ||||
| chr4:5708516-5708644 | Common:2; Rare:73; Clinvar (benign):4 | ||||
| chr4:5711065-5711288 | Rare:150; Clinvar:4 | ||||
| chr4:6269401-6270091 | Common:9; Rare:366; Clinvar:15; Clinvar (benign):2 | ||||
| chr4:6575050-6575222 | Common:6; Rare:121 | ||||
| chr4:6640519-6641089 | Common:6; Rare:274 | ||||
| chr4:6693310-6693590 | Common:2; Rare:96 | ||||
| chr4:6693656-6694052 | Common:1; Rare:153 | ||||
| chr4:6709812-6710007 | Common:2; Rare:100 | ||||
| chr4:6715956-6716227 | Common:1; Rare:187 | ||||
| chr4:6782359-6782816 | Common:5; Rare:316 | ||||
| chr4:6909361-6909494 | Rare:57 | ||||
| chr4:6909673-6909913 | Rare:177 | ||||
| chr4:6987014-6987314 | Common:3; Rare:180 |