Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:110314074-110314162 | Common:2; Rare:18 | ||||
chr13:110424731-110424996 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
chr13:110449486-110449786 | Common:4; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
chr13:110463281-110463444 | Common:5; Rare:22 | ||||
chr13:110503853-110504264 | Common:4; Rare:135; Clinvar:1; Clinvar (benign):3 | ||||
chr13:110870287-110870550 | Common:3; Rare:39 | ||||
chr13:114015580-114015848 | Common:2; Rare:80 | ||||
chr14:20699163-20699458 | Common:1; Rare:67 | ||||
chr14:34764906-34764953 | Rare:10 | ||||
chr14:49633932-49634043 | Common:1; Rare:51; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr14:49789562-49789622 | Rare:16 | ||||
chr14:49862624-49863123 | Common:2; Rare:211 | ||||
chr14:60156123-60156439 | Common:5; Rare:69 | ||||
chr14:61751009-61751207 | Rare:51 | ||||
chr14:68795244-68795413 | Common:3; Rare:38 |