| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122922923-122923137 | Common:2; Rare:62 | ||||
| chr4:123399348-123399654 | Common:1; Rare:92 | ||||
| chr4:127880797-127880937 | Rare:45 | ||||
| chr4:128060994-128061329 | Common:1; Rare:118 | ||||
| chr4:129093494-129093731 | Rare:72 | ||||
| chr4:139301295-139301562 | Common:4; Rare:83 | ||||
| chr4:139302467-139302795 | Common:2; Rare:62 | ||||
| chr4:139453674-139453697 | Common:1; Rare:9 | ||||
| chr4:139453707-139454210 | Common:4; Rare:139; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:140373384-140373680 | Common:2; Rare:113 | ||||
| chr4:142846224-142846352 | Rare:30 | ||||
| chr4:143337102-143337191 | Rare:38 | ||||
| chr4:143513349-143513547 | Common:2; Rare:70 | ||||
| chr4:144019308-144019592 | Common:3; Rare:61 | ||||
| chr4:145098130-145098350 | Rare:73 |