Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:5680920-5681048 | Rare:37 | ||||
chr19:5978078-5978379 | Common:3; Rare:111 | ||||
chr19:6361738-6361801 | Rare:30; Clinvar:1 | ||||
chr19:6393125-6393491 | Common:4; Rare:95 | ||||
chr19:6416845-6417085 | Common:1; Rare:80 | ||||
chr19:6710772-6711065 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
chr19:6714171-6714442 | Common:1; Rare:77; Clinvar (benign):2 | ||||
chr19:6740627-6741099 | Common:1; Rare:121 | ||||
chr19:7294253-7294554 | Common:6; Rare:75 | ||||
chr19:7395025-7395185 | Common:4; Rare:48 | ||||
chr19:7488997-7489103 | Rare:48 | ||||
chr19:7535432-7535740 | Common:3; Rare:93; Clinvar:2 | ||||
chr19:7629478-7629848 | Common:7; Rare:142; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7637003-7637143 | Common:2; Rare:48; Clinvar (benign):1 | ||||
chr19:7943647-7943969 | Rare:79 |