Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:36473557-36473888 | Common:3; Rare:90; Clinvar (benign):1 | ||||
chr1:36475522-36475837 | Common:1; Rare:87; Clinvar:4; Clinvar (benign):2 | ||||
chr1:36479483-36479791 | Common:1; Rare:52 | ||||
chr1:36483240-36483405 | Common:1; Rare:29 | ||||
chr1:37474348-37474587 | Common:1; Rare:92 | ||||
chr1:37514729-37514824 | Rare:64 | ||||
chr1:37595888-37596126 | Common:4; Rare:76 | ||||
chr1:37634662-37634965 | Common:1; Rare:90 | ||||
chr1:37690502-37690759 | Common:6; Rare:68 | ||||
chr1:37692202-37692564 | Common:4; Rare:82 | ||||
chr1:37808177-37808644 | Common:1; Rare:111 | ||||
chr1:37859544-37859820 | Common:4; Rare:97 | ||||
chr1:37989870-37990142 | Rare:90 | ||||
chr1:38859691-38860000 | Rare:121 | ||||
chr1:38873306-38873563 | Common:3; Rare:91 |