Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1774937-1775192 | Common:2; Rare:99; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr17:2174744-2174928 | Rare:33 | ||||
chr17:2399590-2399811 | Common:2; Rare:72 | ||||
chr17:7885908-7886193 | Common:4; Rare:58 | ||||
chr17:7916287-7916399 | Rare:31 | ||||
chr17:8480196-8480494 | Rare:95 | ||||
chr17:8697371-8697663 | Common:2; Rare:59 | ||||
chr17:17752268-17752485 | Common:1; Rare:76 | ||||
chr17:18184883-18185013 | Rare:27 | ||||
chr17:27353779-27354070 | Common:1; Rare:79 | ||||
chr17:32127510-32127617 | Rare:30 | ||||
chr17:35567873-35568147 | Common:2; Rare:85 | ||||
chr17:38452398-38452469 | Common:1; Rare:11 | ||||
chr17:43315651-43315916 | Common:6; Rare:112 | ||||
chr17:43368082-43368345 | Common:9; Rare:105 |