| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139301177-139301568 | Common:6; Rare:110 | ||||
| chr4:139302422-139302552 | Rare:28 | ||||
| chr4:139453659-139453718 | Common:1; Rare:22 | ||||
| chr4:139453770-139454264 | Common:3; Rare:140; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556106-139556310 | Rare:52 | ||||
| chr4:139556383-139556611 | Rare:34 | ||||
| chr4:139606785-139606935 | Rare:32 | ||||
| chr4:139665738-139666026 | Common:2; Rare:65 | ||||
| chr4:140152982-140153234 | Rare:86 | ||||
| chr4:140373357-140373709 | Common:3; Rare:140 | ||||
| chr4:141636510-141636662 | Rare:29 | ||||
| chr4:141636769-141637010 | Common:1; Rare:50 | ||||
| chr4:143184659-143185141 | Common:8; Rare:180 | ||||
| chr4:143336793-143336920 | Rare:35 | ||||
| chr4:145098136-145098379 | Rare:81 |