| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89080581-89080823 | Common:1; Rare:105 | ||||
| chr6:89117950-89118093 | Common:1; Rare:57 | ||||
| chr6:89145983-89146090 | Rare:32 | ||||
| chr6:89352634-89352947 | Common:1; Rare:72 | ||||
| chr6:89411397-89411463 | Rare:12 | ||||
| chr6:89638427-89638577 | Common:1; Rare:33 | ||||
| chr6:89638721-89638829 | Common:3; Rare:38 | ||||
| chr6:89819702-89819877 | Rare:58 | ||||
| chr6:89829600-89829973 | Common:1; Rare:97 | ||||
| chr6:90586986-90587191 | Common:3; Rare:63 | ||||
| chr6:93419538-93419824 | Common:1; Rare:77 | ||||
| chr6:95577356-95577614 | Common:6; Rare:72 | ||||
| chr6:96521671-96521883 | Common:8; Rare:101 | ||||
| chr6:96897778-96898083 | Common:4; Rare:115; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:97283178-97283318 | Common:2; Rare:47 |