| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:142301822-142302154 | Common:6; Rare:97 | ||||
| chr6:143060724-143060920 | Common:7; Rare:67 | ||||
| chr6:143450660-143450961 | Common:1; Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:144285235-144285583 | Common:2; Rare:81 | ||||
| chr6:145814656-145814922 | Common:1; Rare:116 | ||||
| chr6:147204488-147204551 | Common:1; Rare:28 | ||||
| chr6:148342913-148343222 | Common:1; Rare:118 | ||||
| chr6:149546010-149546191 | Common:1; Rare:79 | ||||
| chr6:149749661-149749796 | Rare:77 | ||||
| chr6:151391528-151391835 | Common:3; Rare:82 | ||||
| chr6:151452016-151452548 | Common:5; Rare:189; Clinvar (benign):3 | ||||
| chr6:151808950-151809133 | Rare:41 | ||||
| chr6:155314452-155314620 | Common:2; Rare:53 | ||||
| chr6:158168225-158168388 | Common:2; Rare:59 | ||||
| chr6:158312681-158312890 | Common:5; Rare:48 |