Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:65561157-65561434 | Common:1; Rare:88; Clinvar (benign):1 | ||||
chr17:67717740-67717950 | Rare:66 | ||||
chr17:68247813-68248142 | Common:6; Rare:145 | ||||
chr17:68511624-68512136 | Common:5; Rare:135 | ||||
chr17:70169319-70169550 | Common:1; Rare:61 | ||||
chr17:72120784-72121047 | Rare:70 | ||||
chr17:73192813-73193070 | Common:15; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
chr17:73232218-73232711 | Common:3; Rare:180 | ||||
chr17:74213334-74213583 | Common:4; Rare:56 | ||||
chr17:74431267-74431408 | Rare:35 | ||||
chr17:74466578-74466693 | Rare:36 | ||||
chr17:74776281-74776506 | Common:4; Rare:71 | ||||
chr17:75046929-75047171 | Common:1; Rare:74 | ||||
chr17:75109848-75109994 | Common:2; Rare:44 | ||||
chr17:75131420-75131654 | Common:1; Rare:77 |