Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:4471981-4472333 | Common:6; Rare:135 | ||||
chr19:4474689-4474900 | Common:3; Rare:49 | ||||
chr19:4723747-4724078 | Common:7; Rare:131 | ||||
chr19:5622711-5623207 | Common:5; Rare:199 | ||||
chr19:5680468-5681173 | Rare:209 | ||||
chr19:5978085-5978368 | Common:3; Rare:106 | ||||
chr19:6199501-6199827 | Common:12; Rare:103 | ||||
chr19:6361733-6361835 | Rare:43; Clinvar:1 | ||||
chr19:6372553-6372823 | Common:3; Rare:90 | ||||
chr19:6393421-6393577 | Common:2; Rare:49 | ||||
chr19:7395022-7395197 | Common:4; Rare:55 | ||||
chr19:7489006-7489123 | Rare:53 | ||||
chr19:7629535-7629848 | Common:5; Rare:111; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7680706-7680889 | Common:1; Rare:60 | ||||
chr19:7874300-7874489 | Rare:50 |