| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:78867827-78868003 | Common:1; Rare:49 | ||||
| chr6:79078137-79078614 | Common:2; Rare:390 | ||||
| chr6:79234432-79234764 | Common:3; Rare:99 | ||||
| chr6:79537300-79537680 | Common:5; Rare:229; Clinvar:9 | ||||
| chr6:80004482-80004697 | Common:7; Rare:92 | ||||
| chr6:80106401-80106702 | Common:2; Rare:101; Clinvar (pathogenic):1 | ||||
| chr6:81752590-81752860 | Rare:233 | ||||
| chr6:82247632-82248002 | Common:2; Rare:216 | ||||
| chr6:82363420-82363850 | Common:4; Rare:211 | ||||
| chr6:82364136-82364344 | Common:4; Rare:106 | ||||
| chr6:83065691-83065981 | Common:2; Rare:184 | ||||
| chr6:83067632-83067743 | Common:1; Rare:33 | ||||
| chr6:83193177-83193438 | Common:6; Rare:152 | ||||
| chr6:83430925-83431245 | Common:8; Rare:156 | ||||
| chr6:84227580-84227969 | Common:4; Rare:122 |