| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:80004503-80004683 | Common:3; Rare:41 | ||||
| chr6:80106450-80106741 | Common:1; Rare:106; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:82247693-82247874 | Common:1; Rare:59 | ||||
| chr6:82363496-82363843 | Common:2; Rare:101 | ||||
| chr6:83065687-83065877 | Common:1; Rare:84 | ||||
| chr6:83067589-83067758 | Common:1; Rare:56 | ||||
| chr6:83067864-83068143 | Common:2; Rare:74 | ||||
| chr6:83193200-83193496 | Common:3; Rare:94 | ||||
| chr6:83430962-83431249 | Common:5; Rare:87 | ||||
| chr6:83708763-83708810 | Common:1; Rare:13 | ||||
| chr6:83709145-83709430 | Common:4; Rare:88 | ||||
| chr6:83853263-83853510 | Common:2; Rare:85 | ||||
| chr6:83859604-83859742 | Rare:57 | ||||
| chr6:84227566-84227700 | Rare:31 | ||||
| chr6:84764575-84764682 | Rare:30 |