Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:70096160-70096419 | Rare:70 | ||||
chr15:70097857-70098079 | Common:1; Rare:51 | ||||
chr15:70854126-70854248 | Rare:39 | ||||
chr15:70892516-70892855 | Common:1; Rare:69 | ||||
chr15:71547210-71547365 | Rare:38 | ||||
chr15:72118167-72118418 | Common:2; Rare:78 | ||||
chr15:72231117-72231516 | Common:3; Rare:126 | ||||
chr15:72375957-72376110 | Common:2; Rare:67; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr15:72686147-72686220 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):2 | ||||
chr15:73633368-73633573 | Common:2; Rare:61 | ||||
chr15:73926331-73926479 | Rare:42 | ||||
chr15:73994587-73994730 | Rare:27 | ||||
chr15:74461107-74461314 | Rare:64 | ||||
chr15:74540959-74541257 | Common:3; Rare:102 | ||||
chr15:74843120-74843334 | Common:1; Rare:60 |