Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:50821853-50821883 | Rare:5 | ||||
chr14:51240149-51240305 | Rare:73 | ||||
chr14:51847251-51847268 | Rare:2 | ||||
chr14:51989368-51989633 | Common:2; Rare:80 | ||||
chr14:52707045-52707232 | Common:1; Rare:83 | ||||
chr14:52729823-52730248 | Common:2; Rare:129 | ||||
chr14:53152353-53152520 | Rare:64 | ||||
chr14:54441317-54441510 | Rare:82 | ||||
chr14:54567035-54567223 | Rare:51 | ||||
chr14:54902819-54902939 | Rare:32; Clinvar (benign):1 | ||||
chr14:55027059-55027331 | Common:2; Rare:73 | ||||
chr14:55051522-55051722 | Rare:91 | ||||
chr14:55191532-55191756 | Common:5; Rare:52 | ||||
chr14:55411818-55411945 | Common:2; Rare:60 | ||||
chr14:55580083-55580290 | Common:2; Rare:90 |