Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54199993-54200215 | Rare:54 | ||||
chr1:54715689-54715894 | Common:4; Rare:61 | ||||
chr1:54764472-54764867 | Common:7; Rare:115 | ||||
chr1:54887162-54887431 | Common:3; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
chr1:55039369-55039630 | Common:2; Rare:64; Clinvar:4; Clinvar (benign):1 | ||||
chr1:56645245-56645394 | Common:1; Rare:56 | ||||
chr1:58700054-58700206 | Common:4; Rare:64 | ||||
chr1:58783977-58784384 | Common:1; Rare:110 | ||||
chr1:59296776-59296834 | Common:1; Rare:22 | ||||
chr1:60864804-60865103 | Common:5; Rare:53 | ||||
chr1:60865213-60865394 | Common:1; Rare:36 | ||||
chr1:60865426-60865598 | Common:3; Rare:33 | ||||
chr1:61076966-61077364 | Common:3; Rare:96 | ||||
chr1:61725037-61725198 | Rare:84 | ||||
chr1:61742393-61742540 | Rare:40 |