Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:34558558-34558818 | Common:1; Rare:76 | ||||
chr20:34677086-34677248 | Rare:40 | ||||
chr20:35092618-35092876 | Common:1; Rare:119 | ||||
chr20:35147290-35147386 | Rare:32 | ||||
chr20:35284713-35285027 | Common:2; Rare:79 | ||||
chr20:35664806-35665042 | Common:1; Rare:63 | ||||
chr20:35699343-35699429 | Rare:23 | ||||
chr20:36236441-36236491 | Rare:8 | ||||
chr20:38033426-38033807 | Common:2; Rare:113 | ||||
chr20:44210698-44211105 | Common:5; Rare:146 | ||||
chr20:44531835-44531963 | Rare:44 | ||||
chr20:44966370-44966493 | Rare:51 | ||||
chr20:45857326-45857621 | Common:3; Rare:79 | ||||
chr20:45891240-45891382 | Common:1; Rare:53; Clinvar:3; Clinvar (benign):1 | ||||
chr20:46406613-46406787 | Rare:40 |