| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:83512310-83512640 | Common:5; Rare:81 | ||||
| chr6:83707826-83709588 | Common:17; Rare:724 | ||||
| chr6:83859524-83859759 | Rare:84 | ||||
| chr6:84033401-84034585 | Common:17; Rare:437 | ||||
| chr6:84227575-84227740 | Rare:43 | ||||
| chr6:85593681-85594071 | Common:2; Rare:125 | ||||
| chr6:85642880-85643046 | Common:2; Rare:63 | ||||
| chr6:85643256-85643719 | Common:2; Rare:164 | ||||
| chr6:85643782-85644003 | Common:3; Rare:67 | ||||
| chr6:87155241-87155632 | Rare:114 | ||||
| chr6:87322425-87322662 | Common:3; Rare:87 | ||||
| chr6:87407706-87408043 | Common:1; Rare:69 | ||||
| chr6:87408430-87408684 | Common:3; Rare:50 | ||||
| chr6:87472819-87473214 | Common:2; Rare:131; Clinvar:1; Clinvar (benign):4 | ||||
| chr6:87589950-87590190 | Common:3; Rare:113; Clinvar (benign):4; Clinvar (pathogenic):1 |