Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:42963141-42963433 | Rare:86; Clinvar (pathogenic):1 | ||||
chr6:44251420-44252201 | Common:3; Rare:257 | ||||
chr6:57961366-57961650 | Common:2; Rare:81 | ||||
chr6:71420827-71421014 | Common:1; Rare:59 | ||||
chr6:85678668-85678955 | Rare:111 | ||||
chr6:106781604-106781661 | Rare:11 | ||||
chr6:106782457-106782892 | Common:3; Rare:78 | ||||
chr6:106787375-106787694 | Rare:53 | ||||
chr6:108562704-108562735 | Rare:10 | ||||
chr6:108622769-108622935 | Common:1; Rare:30 | ||||
chr6:113873321-113873410 | Common:1; Rare:17 | ||||
chr6:117999195-117999281 | Common:1; Rare:24 | ||||
chr6:144286211-144286438 | Common:2; Rare:45 | ||||
chr6:157461036-157461210 | Rare:33 | ||||
chr6:158771251-158771561 | Common:1; Rare:82 |