| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:80266394-80266650 | Common:5; Rare:270 | ||||
| chr4:80266789-80267232 | Common:3; Rare:427; Clinvar (pathogenic):3 | ||||
| chr4:80335496-80336309 | Rare:512 | ||||
| chr4:81471796-81472196 | Common:4; Rare:311 | ||||
| chr4:82372443-82372843 | Common:1; Rare:269 | ||||
| chr4:82373020-82374567 | Common:28; Rare:2239 | ||||
| chr4:82428592-82429194 | Common:2; Rare:233 | ||||
| chr4:82429325-82430095 | Common:13; Rare:1510; Clinvar:83; Clinvar (benign):41 | ||||
| chr4:82430051-82430940 | Common:14; Rare:1084 | ||||
| chr4:82890858-82892095 | Common:21; Rare:1048 | ||||
| chr4:82899857-82900336 | Common:2; Rare:191 | ||||
| chr4:82900400-82900882 | Common:3; Rare:674 | ||||
| chr4:82900860-82901326 | Common:11; Rare:795 | ||||
| chr4:82901425-82901536 | Rare:21 | ||||
| chr4:82901634-82902034 | Common:9; Rare:61 |