Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11934539-11934774 | Common:6; Rare:149; Clinvar:10; Clinvar (benign):2 | ||||
chr1:11979940-11980323 | Common:4; Rare:126; Clinvar:1; Clinvar (benign):1 | ||||
chr1:12019233-12019590 | Common:10; Rare:233 | ||||
chr1:12595960-12596370 | Common:4; Rare:76 | ||||
chr1:12617680-12618560 | Common:13; Rare:281 | ||||
chr1:13749253-13749464 | Common:4; Rare:140 | ||||
chr1:15152431-15152569 | Rare:21 | ||||
chr1:15153602-15153797 | Common:3; Rare:100 | ||||
chr1:15356910-15357390 | Common:1; Rare:155 | ||||
chr1:15409792-15409996 | Rare:120 | ||||
chr1:15526450-15526926 | Common:4; Rare:288 | ||||
chr1:15584690-15584990 | Common:7; Rare:183 | ||||
chr1:15585016-15585223 | Common:2; Rare:51 | ||||
chr1:15617167-15617612 | Common:4; Rare:215 | ||||
chr1:15684222-15684523 | Common:4; Rare:114 |