| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:80004497-80004640 | Common:2; Rare:32 | ||||
| chr6:81752652-81752821 | Rare:87 | ||||
| chr6:83067612-83067750 | Common:1; Rare:47 | ||||
| chr6:83193194-83193389 | Common:3; Rare:63 | ||||
| chr6:85449529-85449727 | Common:1; Rare:50 | ||||
| chr6:85449854-85450090 | Common:1; Rare:62 | ||||
| chr6:85593828-85594098 | Common:1; Rare:75 | ||||
| chr6:87155268-87155594 | Rare:87 | ||||
| chr6:87472900-87473004 | Common:1; Rare:40; Clinvar (benign):4 | ||||
| chr6:87589920-87590159 | Common:2; Rare:119; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr6:89638725-89638843 | Common:3; Rare:38 | ||||
| chr6:89829609-89829909 | Rare:69 | ||||
| chr6:95577404-95577553 | Common:3; Rare:41 | ||||
| chr6:96521476-96521883 | Common:10; Rare:163 | ||||
| chr6:96897807-96898077 | Common:4; Rare:102; Clinvar:3; Clinvar (benign):1 |