| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:139028610-139028866 | Common:1; Rare:56 | ||||
| chr6:142147140-142147340 | Rare:89 | ||||
| chr6:142301848-142302179 | Common:6; Rare:94 | ||||
| chr6:142302471-142302690 | Common:1; Rare:42 | ||||
| chr6:142945145-142945459 | Common:1; Rare:73 | ||||
| chr6:142945696-142945981 | Common:1; Rare:64 | ||||
| chr6:143060391-143060488 | Rare:23 | ||||
| chr6:143060707-143060935 | Common:7; Rare:80 | ||||
| chr6:143450660-143450961 | Common:1; Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511651-143511837 | Common:4; Rare:45 | ||||
| chr6:143843151-143843443 | Common:2; Rare:94 | ||||
| chr6:144095504-144095840 | Common:6; Rare:100 | ||||
| chr6:144150331-144150586 | Common:5; Rare:69 | ||||
| chr6:144285153-144285725 | Common:5; Rare:150 | ||||
| chr6:145814649-145814971 | Common:1; Rare:140 |