Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73463592-73463710 | Common:1; Rare:22 | ||||
chr14:73567603-73567621 | Rare:8 | ||||
chr14:73567916-73568128 | Rare:58 | ||||
chr14:73569053-73569303 | Rare:59 | ||||
chr14:73592103-73592185 | Common:1; Rare:39 | ||||
chr14:73610663-73610945 | Common:2; Rare:35 | ||||
chr14:73787166-73787371 | Common:2; Rare:76 | ||||
chr14:73851592-73851983 | Common:4; Rare:112 | ||||
chr14:73950050-73950350 | Common:6; Rare:137; Clinvar (benign):5 | ||||
chr14:73961401-73961736 | Common:3; Rare:77; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:74019201-74019432 | Common:2; Rare:92 | ||||
chr14:74084365-74084799 | Common:7; Rare:116 | ||||
chr14:74493219-74493782 | Common:4; Rare:181; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:74713052-74713207 | Rare:87 | ||||
chr14:74809715-74809945 | Rare:65 |