| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:235511446-235511810 | Common:4; Rare:71 | ||||
| chr2:237577348-237577444 | Rare:34 | ||||
| chr2:237577467-237577645 | Common:2; Rare:39 | ||||
| chr2:240456697-240456705 | Rare:2 | ||||
| chr2:241233893-241234239 | Common:2; Rare:75 | ||||
| chr2:242088376-242088727 | Common:13; Rare:125 | ||||
| chr20:420581-420899 | Common:4; Rare:56; Clinvar (benign):1 | ||||
| chr20:1326754-1326929 | Rare:22 | ||||
| chr20:1427827-1427981 | Common:2; Rare:37 | ||||
| chr20:3200058-3200459 | Common:1; Rare:110 | ||||
| chr20:3203879-3204075 | Common:3; Rare:50 | ||||
| chr20:3784377-3784662 | Rare:58 | ||||
| chr20:6025589-6025709 | Common:1; Rare:19 | ||||
| chr20:6769983-6770165 | Rare:53 | ||||
| chr20:10643581-10643814 | Common:2; Rare:50; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |