Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6579793-6580063 | Common:4; Rare:91 | ||||
chr1:6602867-6603122 | Common:3; Rare:87 | ||||
chr1:6701727-6701976 | Rare:74 | ||||
chr1:7771176-7771368 | Common:3; Rare:87 | ||||
chr1:7784068-7784318 | Rare:103 | ||||
chr1:7953970-7954037 | Rare:17 | ||||
chr1:7954165-7954341 | Rare:59 | ||||
chr1:7961449-7961966 | Common:6; Rare:167; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:8026304-8026500 | Common:2; Rare:86 | ||||
chr1:8878578-8878874 | Rare:157 | ||||
chr1:8879194-8879388 | Common:2; Rare:66 | ||||
chr1:8879604-8879772 | Common:1; Rare:28 | ||||
chr1:9942711-9942906 | Common:1; Rare:31 | ||||
chr1:9943016-9943500 | Common:7; Rare:125 | ||||
chr1:10032647-10032980 | Common:3; Rare:90 |