Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:5950467-5950667 | Common:8; Rare:55 | ||||
chr20:13784894-13785053 | Common:2; Rare:65; Clinvar (benign):2 | ||||
chr20:17968449-17968591 | Common:4; Rare:58 | ||||
chr20:17968792-17969073 | Common:2; Rare:106 | ||||
chr20:21303247-21303372 | Rare:51 | ||||
chr20:31739107-31739358 | Common:1; Rare:63 | ||||
chr20:32207729-32207932 | Common:3; Rare:78 | ||||
chr20:35699305-35699451 | Rare:49; Clinvar (benign):3 | ||||
chr20:38033423-38033757 | Common:2; Rare:97 | ||||
chr20:44966411-44966531 | Rare:40 | ||||
chr20:45791920-45791989 | Rare:22 | ||||
chr20:45891026-45891358 | Common:3; Rare:97; Clinvar:7; Clinvar (benign):3 | ||||
chr20:49278036-49278259 | Rare:59 | ||||
chr20:50958519-50958834 | Common:1; Rare:93; Clinvar (benign):1 | ||||
chr20:56392187-56392397 | Rare:54 |