Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:73232220-73232438 | Rare:99 | ||||
chr17:74776288-74776512 | Common:4; Rare:67 | ||||
chr17:75046935-75047201 | Common:1; Rare:79 | ||||
chr17:75130788-75131054 | Common:2; Rare:88 | ||||
chr17:75131698-75131881 | Common:4; Rare:85 | ||||
chr17:75261588-75261969 | Common:4; Rare:128; Clinvar (benign):4 | ||||
chr17:75393737-75394020 | Common:1; Rare:68 | ||||
chr17:75667136-75667370 | Common:4; Rare:74 | ||||
chr17:75979121-75979310 | Rare:50; Clinvar:4 | ||||
chr17:75979420-75979457 | Rare:10 | ||||
chr17:76103711-76103859 | Common:3; Rare:47 | ||||
chr17:76726525-76726886 | Common:5; Rare:135 | ||||
chr17:76737329-76737698 | Common:3; Rare:126 | ||||
chr17:78186985-78187364 | Common:3; Rare:130 | ||||
chr17:80036587-80036658 | Common:2; Rare:17; Clinvar (benign):2 |