Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6667510-6667930 | Common:2; Rare:195 | ||||
chr1:6701731-6702020 | Rare:161 | ||||
chr1:6784948-6785454 | Common:2; Rare:256 | ||||
chr1:7771146-7771381 | Common:8; Rare:188 | ||||
chr1:7784020-7784360 | Rare:203 | ||||
chr1:7953990-7954470 | Common:7; Rare:219 | ||||
chr1:7961439-7961793 | Common:8; Rare:239; Clinvar:5; Clinvar (benign):6 | ||||
chr1:8026304-8026450 | Rare:62 | ||||
chr1:8656012-8656750 | Common:6; Rare:263; Clinvar:2; Clinvar (benign):2 | ||||
chr1:8703081-8704050 | Common:5; Rare:388 | ||||
chr1:8817603-8817888 | Common:4; Rare:181 | ||||
chr1:8877897-8878297 | Common:3; Rare:142 | ||||
chr1:8878560-8878950 | Rare:351 | ||||
chr1:8879183-8879386 | Common:5; Rare:133 | ||||
chr1:9234547-9235012 | Common:16; Rare:355 |