| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89819681-89819856 | Rare:60 | ||||
| chr6:89829609-89829914 | Rare:70 | ||||
| chr6:95577407-95577538 | Common:3; Rare:36 | ||||
| chr6:96521679-96521876 | Common:7; Rare:96 | ||||
| chr6:96897817-96898044 | Common:4; Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:97283179-97283424 | Common:3; Rare:73 | ||||
| chr6:99425259-99425506 | Common:2; Rare:69 | ||||
| chr6:100464881-100465130 | Common:2; Rare:71 | ||||
| chr6:100881261-100881482 | Common:5; Rare:91 | ||||
| chr6:104859827-104860010 | Common:1; Rare:62 | ||||
| chr6:106086210-106086381 | Rare:42 | ||||
| chr6:106629446-106629649 | Common:3; Rare:48 | ||||
| chr6:106975270-106975510 | Common:1; Rare:70 | ||||
| chr6:107459470-107459692 | Common:1; Rare:57; Clinvar:1 | ||||
| chr6:107958069-107958398 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):3 |