Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:58692495-58692675 | Common:2; Rare:97; Clinvar:13; Clinvar (benign):20 | ||||
chr17:59106670-59107015 | Common:3; Rare:115; Clinvar:5; Clinvar (benign):4 | ||||
chr17:59155138-59155520 | Common:2; Rare:86 | ||||
chr17:59331445-59331791 | Common:2; Rare:114 | ||||
chr17:59619204-59619359 | Common:1; Rare:43 | ||||
chr17:59619562-59620058 | Common:3; Rare:175 | ||||
chr17:59707392-59707541 | Common:1; Rare:39; Clinvar (benign):4 | ||||
chr17:59837506-59838032 | Common:1; Rare:76 | ||||
chr17:59892744-59893161 | Common:1; Rare:115 | ||||
chr17:59964690-59964861 | Common:2; Rare:72 | ||||
chr17:60078910-60078982 | Common:4; Rare:37 | ||||
chr17:60391998-60392321 | Common:2; Rare:81 | ||||
chr17:60525907-60526290 | Common:2; Rare:128 | ||||
chr17:61927953-61928160 | Common:1; Rare:67 | ||||
chr17:62477848-62478062 | Common:1; Rare:66 |