Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:74776281-74776540 | Common:4; Rare:87 | ||||
chr17:75205370-75205730 | Common:1; Rare:108 | ||||
chr17:75261590-75261945 | Common:4; Rare:114; Clinvar (benign):2 | ||||
chr17:75271165-75271369 | Common:2; Rare:38 | ||||
chr17:75289387-75289651 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
chr17:75393760-75394023 | Common:1; Rare:59 | ||||
chr17:75667131-75667399 | Common:4; Rare:93 | ||||
chr17:75784564-75784875 | Common:2; Rare:139 | ||||
chr17:75979103-75979276 | Rare:48; Clinvar:4 | ||||
chr17:75979369-75979581 | Common:1; Rare:62; Clinvar (benign):1 | ||||
chr17:76103703-76103867 | Common:4; Rare:57 | ||||
chr17:76353609-76353865 | Common:2; Rare:91 | ||||
chr17:76726491-76726910 | Common:5; Rare:159 | ||||
chr17:76737325-76737542 | Common:2; Rare:83 | ||||
chr17:76737887-76738129 | Common:4; Rare:70 |