| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:113970323-113970533 | Common:1; Rare:71 | ||||
| chr6:113970922-113971449 | Common:5; Rare:210 | ||||
| chr6:116100672-116100933 | Common:1; Rare:111 | ||||
| chr6:116253974-116254265 | Common:6; Rare:86 | ||||
| chr6:116279245-116279469 | Common:3; Rare:92 | ||||
| chr6:116279731-116280120 | Common:2; Rare:131 | ||||
| chr6:116571164-116571618 | Common:3; Rare:133 | ||||
| chr6:116616275-116616416 | Common:3; Rare:26 | ||||
| chr6:116680990-116681296 | Common:4; Rare:88 | ||||
| chr6:117602143-117602259 | Rare:44 | ||||
| chr6:117602397-117602648 | Common:4; Rare:66 | ||||
| chr6:117675305-117675498 | Common:3; Rare:53 | ||||
| chr6:117675747-117675921 | Rare:64 | ||||
| chr6:117907584-117907738 | Rare:44 | ||||
| chr6:118548163-118548392 | Common:2; Rare:47; Clinvar:4; Clinvar (benign):2 |