Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:31604331-31604428 | Rare:35 | ||||
chr20:35490966-35491051 | Rare:17 | ||||
chr20:36049940-36050163 | Common:1; Rare:48 | ||||
chr20:36050281-36050729 | Common:2; Rare:153 | ||||
chr20:36890163-36890317 | Rare:25 | ||||
chr20:44180895-44181105 | Rare:33 | ||||
chr20:44188909-44189095 | Common:1; Rare:36 | ||||
chr20:44724528-44724796 | Common:1; Rare:67 | ||||
chr20:45894708-45894888 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
chr20:47352502-47352664 | Rare:28 | ||||
chr20:47357792-47357903 | Rare:17 | ||||
chr20:47358848-47358940 | Rare:17 | ||||
chr20:49483359-49483709 | Common:3; Rare:85 | ||||
chr20:50192067-50192318 | Common:2; Rare:73 | ||||
chr20:50267456-50267506 | Common:1; Rare:7 |