Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:77458378-77458445 | Rare:14 | ||||
chr17:77492681-77493010 | Common:2; Rare:74; Clinvar (benign):2 | ||||
chr17:77942412-77942656 | Common:2; Rare:49 | ||||
chr17:78442827-78443139 | Common:2; Rare:77 | ||||
chr17:78862169-78862252 | Rare:18 | ||||
chr17:78882961-78883241 | Common:1; Rare:53 | ||||
chr17:78883773-78884122 | Common:1; Rare:84 | ||||
chr17:78986660-78986839 | Common:1; Rare:35 | ||||
chr17:79844109-79844290 | Rare:48 | ||||
chr17:79948870-79949233 | Common:2; Rare:107 | ||||
chr17:79949963-79950275 | Rare:60 | ||||
chr17:79953138-79953247 | Common:2; Rare:16 | ||||
chr17:79960366-79960764 | Rare:63 | ||||
chr17:79960889-79961197 | Common:2; Rare:45 | ||||
chr17:80156026-80156058 | Rare:5 |