Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:38033423-38033767 | Common:2; Rare:100 | ||||
chr20:38962148-38962382 | Common:1; Rare:97 | ||||
chr20:43590650-43590986 | Rare:74 | ||||
chr20:44210737-44211105 | Common:5; Rare:129 | ||||
chr20:44475811-44475905 | Rare:33 | ||||
chr20:44531796-44531978 | Common:1; Rare:58 | ||||
chr20:44966370-44966557 | Rare:74 | ||||
chr20:45348394-45348593 | Common:1; Rare:58 | ||||
chr20:45857326-45857584 | Common:3; Rare:71 | ||||
chr20:45891020-45891387 | Common:3; Rare:109; Clinvar:8; Clinvar (benign):3 | ||||
chr20:46406577-46406785 | Common:1; Rare:52 | ||||
chr20:46513525-46513612 | Common:1; Rare:30 | ||||
chr20:47356664-47356887 | Rare:51 | ||||
chr20:47501764-47501993 | Common:1; Rare:78 | ||||
chr20:49278039-49278272 | Rare:65 |