Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153990655-153990830 | Common:2; Rare:86 | ||||
chr1:154182986-154183290 | Rare:97 | ||||
chr1:154220499-154221004 | Common:1; Rare:172 | ||||
chr1:154272266-154272773 | Common:6; Rare:123; Clinvar:3; Clinvar (benign):3 | ||||
chr1:154501987-154502170 | Common:1; Rare:55 | ||||
chr1:154627910-154628013 | Common:2; Rare:53 | ||||
chr1:154936603-154936780 | Common:2; Rare:61 | ||||
chr1:154956085-154956258 | Common:1; Rare:51 | ||||
chr1:154961731-154962037 | Common:1; Rare:107 | ||||
chr1:154970703-154970846 | Rare:29 | ||||
chr1:154974322-154974730 | Rare:104 | ||||
chr1:154983085-154983388 | Common:2; Rare:59 | ||||
chr1:155051131-155051389 | Common:2; Rare:91 | ||||
chr1:155135707-155135892 | Common:2; Rare:80 | ||||
chr1:155207877-155207974 | Rare:24 |