| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:110981959-110982100 | Common:2; Rare:68 | ||||
| chr6:111483211-111483642 | Common:1; Rare:156 | ||||
| chr6:112087414-112087708 | Rare:91 | ||||
| chr6:113857247-113857449 | Common:1; Rare:47 | ||||
| chr6:113970312-113970370 | Rare:17 | ||||
| chr6:113970656-113970800 | Rare:43 | ||||
| chr6:113970915-113971192 | Common:2; Rare:135 | ||||
| chr6:116254046-116254251 | Common:4; Rare:58 | ||||
| chr6:116279833-116280114 | Common:2; Rare:96 | ||||
| chr6:116571164-116571613 | Common:3; Rare:132 | ||||
| chr6:116681002-116681313 | Common:4; Rare:86 | ||||
| chr6:117602451-117602677 | Common:3; Rare:64 | ||||
| chr6:117906920-117907281 | Common:4; Rare:125 | ||||
| chr6:118548282-118548362 | Common:1; Rare:14; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:118893908-118894241 | Common:3; Rare:99 |