Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:67360062-67360402 | Common:4; Rare:89 | ||||
chr14:68793049-68793183 | Rare:32 | ||||
chr14:68979181-68979495 | Common:2; Rare:90 | ||||
chr14:69398251-69398403 | Rare:62 | ||||
chr14:69398617-69398740 | Rare:31 | ||||
chr14:69611462-69611732 | Common:1; Rare:88 | ||||
chr14:70417010-70417124 | Rare:29 | ||||
chr14:72926175-72926524 | Common:6; Rare:87 | ||||
chr14:73058303-73058585 | Common:3; Rare:85 | ||||
chr14:73569061-73569085 | Rare:4 | ||||
chr14:73644891-73645036 | Common:2; Rare:41; Clinvar:2 | ||||
chr14:73851691-73851860 | Common:1; Rare:47 | ||||
chr14:73950083-73950323 | Common:5; Rare:95; Clinvar (benign):3 | ||||
chr14:74019259-74019455 | Common:1; Rare:73 | ||||
chr14:74493249-74493777 | Common:4; Rare:168; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 |