Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40121821-40121982 | Common:1; Rare:59 | ||||
chr17:40140212-40140569 | Common:5; Rare:182 | ||||
chr17:41812614-41813013 | Common:3; Rare:86; Clinvar:5 | ||||
chr17:42536048-42536310 | Common:3; Rare:81; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr17:42577678-42577849 | Rare:84 | ||||
chr17:42609306-42609744 | Common:8; Rare:186; Clinvar (benign):2 | ||||
chr17:42659365-42659387 | Rare:6 | ||||
chr17:42682409-42682537 | Rare:27 | ||||
chr17:42798661-42798785 | Rare:40 | ||||
chr17:42964411-42964536 | Rare:59 | ||||
chr17:42980459-42980576 | Common:1; Rare:47 | ||||
chr17:43170204-43170397 | Rare:42 | ||||
chr17:43211778-43211897 | Common:1; Rare:26 | ||||
chr17:44070583-44070940 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44123611-44123864 | Common:3; Rare:71 |