| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122732459-122732762 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922955-122923137 | Common:2; Rare:59 | ||||
| chr4:127632765-127632966 | Common:1; Rare:49 | ||||
| chr4:127880764-127880940 | Rare:62 | ||||
| chr4:133149087-133149301 | Common:2; Rare:65 | ||||
| chr4:137532457-137532623 | Rare:28 | ||||
| chr4:139084323-139084548 | Common:3; Rare:101 | ||||
| chr4:139301271-139301557 | Common:4; Rare:86 | ||||
| chr4:139453770-139454185 | Common:3; Rare:104; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556193-139556383 | Rare:42 | ||||
| chr4:140373380-140373698 | Common:2; Rare:127 | ||||
| chr4:143513668-143513750 | Rare:26 | ||||
| chr4:145098148-145098361 | Rare:75 | ||||
| chr4:147617213-147617463 | Common:1; Rare:58 | ||||
| chr4:151015728-151015861 | Rare:64 |