Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:33812304-33812330 | Rare:4 | ||||
chr20:35173592-35173879 | Common:2; Rare:47 | ||||
chr20:35490957-35491116 | Rare:30 | ||||
chr20:36050290-36050494 | Common:1; Rare:56 | ||||
chr20:36050498-36050729 | Common:1; Rare:90 | ||||
chr20:36950860-36950928 | Rare:10 | ||||
chr20:38146815-38147004 | Rare:58 | ||||
chr20:38446652-38446756 | Common:1; Rare:45 | ||||
chr20:40686522-40686585 | Rare:9; Clinvar (benign):1 | ||||
chr20:40687248-40687484 | Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
chr20:40687530-40687840 | Rare:56; Clinvar:2; Clinvar (benign):3 | ||||
chr20:40687891-40688037 | Rare:44 | ||||
chr20:40688192-40688282 | Rare:28 | ||||
chr20:41030607-41030664 | Rare:9 | ||||
chr20:44188921-44189091 | Rare:33 |