| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:3207570-3208134 | Rare:163 | ||||
| chr4:3285541-3285855 | Common:6; Rare:128 | ||||
| chr4:3408051-3408390 | Rare:112 | ||||
| chr4:3955403-3955644 | Common:8; Rare:72 | ||||
| chr4:4473750-4473978 | Common:2; Rare:71 | ||||
| chr4:4852521-4853867 | Common:18; Rare:564 | ||||
| chr4:4856671-4857179 | Common:17; Rare:286 | ||||
| chr4:6277110-6277640 | Common:15; Rare:254; Clinvar:15; Clinvar (benign):19; Clinvar (pathogenic):1 | ||||
| chr4:6673185-6673467 | Common:6; Rare:134 | ||||
| chr4:6673815-6674130 | Common:24; Rare:282 | ||||
| chr4:6689908-6690308 | Common:6; Rare:136 | ||||
| chr4:6732665-6732851 | Common:2; Rare:74 | ||||
| chr4:6733490-6733940 | Common:4; Rare:110 | ||||
| chr4:6749370-6749740 | Common:7; Rare:96 | ||||
| chr4:6753080-6753332 | Common:5; Rare:107 |