Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:110213779-110214017 | Common:2; Rare:59; Clinvar (benign):2 | ||||
chr13:110308006-110308146 | Common:1; Rare:45 | ||||
chr13:110409533-110409671 | Common:2; Rare:23 | ||||
chr13:110424731-110424996 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
chr13:110503841-110504264 | Common:4; Rare:142; Clinvar:1; Clinvar (benign):4 | ||||
chr13:110870281-110870584 | Common:3; Rare:42 | ||||
chr14:22547344-22547542 | Common:2; Rare:50 | ||||
chr14:38254377-38254931 | Rare:162 | ||||
chr14:49633956-49634043 | Common:1; Rare:40; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49862655-49862969 | Common:1; Rare:151 | ||||
chr14:51396253-51396622 | Common:2; Rare:78 | ||||
chr14:73245963-73246108 | Common:2; Rare:60 | ||||
chr14:74502891-74503230 | Common:1; Rare:93; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr14:85530950-85531125 | Common:1; Rare:31 | ||||
chr14:100825971-100826139 | Rare:29 |