Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7857461-7857756 | Common:2; Rare:96 | ||||
chr17:7885187-7885349 | Rare:51 | ||||
chr17:7931869-7932235 | Common:5; Rare:96 | ||||
chr17:8152385-8152556 | Common:2; Rare:37 | ||||
chr17:8435706-8436002 | Common:4; Rare:120 | ||||
chr17:10697503-10697653 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
chr17:11997436-11997602 | Rare:56 | ||||
chr17:14069395-14069572 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):3 | ||||
chr17:14300773-14301103 | Common:2; Rare:88 | ||||
chr17:15699454-15699768 | Common:4; Rare:85 | ||||
chr17:15999611-16000005 | Common:3; Rare:175; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr17:17281170-17281233 | Rare:32 | ||||
chr17:17591626-17591936 | Common:1; Rare:90 | ||||
chr17:18087822-18088001 | Rare:51 | ||||
chr17:18254547-18254823 | Rare:98 |