Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:59565483-59565674 | Common:1; Rare:77 | ||||
chr17:59619557-59620025 | Common:3; Rare:162 | ||||
chr17:59620029-59620139 | Rare:39 | ||||
chr17:59707386-59707732 | Common:3; Rare:96; Clinvar (benign):4 | ||||
chr17:59892705-59893254 | Common:1; Rare:154 | ||||
chr17:59964699-59965096 | Common:2; Rare:122 | ||||
chr17:60078910-60078993 | Common:4; Rare:41 | ||||
chr17:60391998-60392248 | Common:2; Rare:62 | ||||
chr17:60525934-60525998 | Common:2; Rare:19 | ||||
chr17:60526160-60526311 | Rare:61 | ||||
chr17:63446037-63446114 | Rare:15 | ||||
chr17:63601177-63601348 | Rare:52; Clinvar:3; Clinvar (benign):1 | ||||
chr17:63741765-63741860 | Rare:27 | ||||
chr17:63773474-63773835 | Common:2; Rare:118 | ||||
chr17:63827040-63827503 | Common:5; Rare:140 |