| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139083903-139084003 | Rare:17 | ||||
| chr4:139084180-139084268 | Rare:41 | ||||
| chr4:139084278-139084543 | Common:4; Rare:115 | ||||
| chr4:139300651-139300737 | Rare:10 | ||||
| chr4:139301214-139301768 | Common:6; Rare:161 | ||||
| chr4:139302290-139302323 | Rare:9 | ||||
| chr4:139302443-139302564 | Common:1; Rare:26 | ||||
| chr4:139453637-139454254 | Common:5; Rare:190; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556109-139556622 | Rare:101 | ||||
| chr4:139606677-139606747 | Rare:17 | ||||
| chr4:139665694-139666036 | Common:2; Rare:78 | ||||
| chr4:140153323-140153428 | Rare:23 | ||||
| chr4:140154062-140154195 | Common:1; Rare:41 | ||||
| chr4:140154197-140154288 | Rare:42 | ||||
| chr4:140373279-140373732 | Common:3; Rare:169 |