| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30647367-30647466 | Common:2; Rare:34 | ||||
| chr6:30717240-30717437 | Common:1; Rare:40 | ||||
| chr6:30720238-30720563 | Common:1; Rare:77 | ||||
| chr6:30742462-30742550 | Common:1; Rare:19 | ||||
| chr6:30742569-30742972 | Common:2; Rare:96 | ||||
| chr6:30744503-30744605 | Common:2; Rare:37 | ||||
| chr6:30886510-30886676 | Rare:23 | ||||
| chr6:30914080-30914351 | Common:2; Rare:89; Clinvar (benign):1 | ||||
| chr6:31158155-31158605 | Common:8; Rare:113 | ||||
| chr6:31541695-31542365 | Common:9; Rare:196 | ||||
| chr6:31542422-31542538 | Rare:35 | ||||
| chr6:31547428-31547724 | Common:2; Rare:78 | ||||
| chr6:31620355-31620703 | Common:1; Rare:101 | ||||
| chr6:31620705-31620835 | Rare:44 | ||||
| chr6:31636220-31636600 | Common:4; Rare:123 |