Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:57182101-57182208 | Rare:22 | ||||
chr6:57194790-57194955 | Rare:36; Clinvar (pathogenic):1 | ||||
chr6:63339917-63340013 | Rare:19 | ||||
chr6:63440053-63440313 | Common:4; Rare:52 | ||||
chr6:63441380-63441907 | Common:2; Rare:98 | ||||
chr6:63442078-63442158 | Common:1; Rare:21 | ||||
chr6:63442323-63442407 | Rare:26 | ||||
chr6:63565096-63565143 | Rare:8 | ||||
chr6:63698297-63698510 | Rare:67 | ||||
chr6:75415500-75415532 | Rare:3 | ||||
chr6:75675209-75675277 | Rare:13 | ||||
chr6:75712961-75713125 | Common:1; Rare:33 | ||||
chr6:79202049-79202386 | Common:1; Rare:96 | ||||
chr6:82210710-82210892 | Common:1; Rare:39 | ||||
chr6:83302397-83302509 | Rare:21 |