Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:5680474-5681209 | Rare:215 | ||||
chr19:5681645-5681869 | Rare:49 | ||||
chr19:5720135-5720366 | Rare:82 | ||||
chr19:5791122-5791272 | Common:3; Rare:58 | ||||
chr19:5903695-5903906 | Common:1; Rare:103; Clinvar:3; Clinvar (benign):3 | ||||
chr19:5978078-5978415 | Common:3; Rare:130 | ||||
chr19:6110426-6110834 | Common:2; Rare:121 | ||||
chr19:6199453-6199866 | Common:13; Rare:129 | ||||
chr19:6216961-6217318 | Common:1; Rare:66 | ||||
chr19:6361453-6361969 | Common:2; Rare:194; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr19:6372519-6372827 | Common:5; Rare:105 | ||||
chr19:6373187-6373477 | Rare:37 | ||||
chr19:6393070-6393226 | Common:3; Rare:40 | ||||
chr19:6393366-6393769 | Common:5; Rare:119 | ||||
chr19:6393956-6394015 | Rare:19 |