| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:139374469-139374660 | Common:1; Rare:94 | ||||
| chr6:142147194-142147287 | Rare:36 | ||||
| chr6:142301832-142302154 | Common:6; Rare:94 | ||||
| chr6:143060724-143060926 | Common:7; Rare:71 | ||||
| chr6:143450660-143450921 | Common:1; Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511628-143511755 | Common:3; Rare:31 | ||||
| chr6:144285178-144285510 | Common:3; Rare:86 | ||||
| chr6:144286158-144286332 | Common:2; Rare:32 | ||||
| chr6:145814669-145814921 | Common:1; Rare:114 | ||||
| chr6:147204454-147204550 | Common:1; Rare:35 | ||||
| chr6:148342879-148343070 | Rare:48 | ||||
| chr6:149546010-149546135 | Rare:53 | ||||
| chr6:149718055-149718409 | Common:5; Rare:95 | ||||
| chr6:149749573-149749796 | Rare:110 | ||||
| chr6:151240240-151240421 | Common:1; Rare:49 |