Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6208680-6208868 | Common:1; Rare:51 | ||||
chr1:6419891-6420011 | Rare:37 | ||||
chr1:6602865-6603107 | Common:3; Rare:88 | ||||
chr1:6785340-6785545 | Common:2; Rare:58 | ||||
chr1:7771146-7771368 | Common:4; Rare:93 | ||||
chr1:7954188-7954293 | Rare:25 | ||||
chr1:7961455-7961785 | Common:4; Rare:110; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8878578-8878874 | Rare:157 | ||||
chr1:9943280-9943488 | Common:2; Rare:53 | ||||
chr1:11099740-11099946 | Common:3; Rare:85 | ||||
chr1:11262493-11262780 | Common:2; Rare:88 | ||||
chr1:11273430-11273515 | Common:1; Rare:29; Clinvar (benign):1 | ||||
chr1:11805921-11806265 | Common:2; Rare:91; Clinvar:1 | ||||
chr1:11934485-11934754 | Common:5; Rare:88; Clinvar:5; Clinvar (benign):1 | ||||
chr1:12616638-12616911 | Common:1; Rare:46 |