Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75012536-75012687 | Common:1; Rare:37 | ||||
chr17:75046933-75047191 | Common:1; Rare:77 | ||||
chr17:75093356-75093536 | Common:1; Rare:45 | ||||
chr17:75109853-75109969 | Common:2; Rare:32 | ||||
chr17:75261598-75261909 | Common:4; Rare:90; Clinvar (benign):1 | ||||
chr17:75639976-75640120 | Common:1; Rare:35 | ||||
chr17:75646061-75646348 | Common:4; Rare:65 | ||||
chr17:75667169-75667370 | Common:4; Rare:62 | ||||
chr17:75844703-75844960 | Common:1; Rare:54 | ||||
chr17:75979091-75979271 | Rare:51; Clinvar:4 | ||||
chr17:76726546-76726860 | Common:5; Rare:106 | ||||
chr17:76737325-76737526 | Common:2; Rare:75 | ||||
chr17:78186980-78187364 | Common:3; Rare:132 | ||||
chr17:78736798-78736977 | Common:1; Rare:34 | ||||
chr17:81295278-81295461 | Common:2; Rare:47 |