Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:45891220-45891379 | Common:1; Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
chr20:45896128-45896427 | Common:3; Rare:79 | ||||
chr20:45897477-45897788 | Common:1; Rare:60; Clinvar (pathogenic):1 | ||||
chr20:45912097-45912273 | Common:3; Rare:43 | ||||
chr20:45934471-45934730 | Common:2; Rare:110 | ||||
chr20:45935027-45935339 | Rare:130 | ||||
chr20:45971753-45971993 | Common:3; Rare:73 | ||||
chr20:46363940-46364042 | Common:1; Rare:17 | ||||
chr20:46364356-46364544 | Rare:69 | ||||
chr20:46406565-46406827 | Common:4; Rare:71 | ||||
chr20:46689416-46689726 | Common:1; Rare:80 | ||||
chr20:47318731-47318822 | Rare:28 | ||||
chr20:47318982-47319114 | Common:1; Rare:35 | ||||
chr20:47356657-47356887 | Rare:54 | ||||
chr20:47501807-47501822 | Rare:2 |