Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:67245174-67245288 | Rare:38 | ||||
chr17:67717660-67717956 | Common:2; Rare:95 | ||||
chr17:68247889-68248136 | Common:6; Rare:104 | ||||
chr17:73232268-73232468 | Rare:79 | ||||
chr17:74776335-74776535 | Common:4; Rare:64 | ||||
chr17:75261598-75261915 | Common:4; Rare:94; Clinvar (benign):1 | ||||
chr17:75667179-75667398 | Common:4; Rare:74 | ||||
chr17:75756462-75756831 | Rare:152; Clinvar:4; Clinvar (benign):1 | ||||
chr17:75784564-75784856 | Common:2; Rare:129 | ||||
chr17:75904882-75905202 | Common:3; Rare:88 | ||||
chr17:75979112-75979245 | Rare:35; Clinvar:2 | ||||
chr17:76726487-76726882 | Common:5; Rare:145 | ||||
chr17:78187043-78187348 | Common:3; Rare:91 | ||||
chr17:78979943-78980202 | Common:2; Rare:54 | ||||
chr17:81666552-81666763 | Common:1; Rare:92 |