Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:59619581-59619994 | Common:3; Rare:150 | ||||
chr17:59707403-59707736 | Common:3; Rare:90; Clinvar (benign):2 | ||||
chr17:59892902-59893140 | Rare:67 | ||||
chr17:63773517-63773818 | Common:2; Rare:101 | ||||
chr17:63827057-63827399 | Common:5; Rare:84 | ||||
chr17:65056592-65056937 | Common:4; Rare:142 | ||||
chr17:68247907-68248137 | Common:6; Rare:97 | ||||
chr17:73232106-73232455 | Common:1; Rare:160 | ||||
chr17:74776329-74776512 | Common:4; Rare:51 | ||||
chr17:75261598-75261939 | Common:4; Rare:106; Clinvar (benign):2 | ||||
chr17:75393764-75394066 | Common:1; Rare:65 | ||||
chr17:75667173-75667364 | Common:4; Rare:57 | ||||
chr17:75979132-75979271 | Rare:38; Clinvar:4 | ||||
chr17:76726497-76726882 | Common:5; Rare:139 | ||||
chr17:76737329-76737577 | Common:2; Rare:91 |