Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:50116530-50116720 | Common:1; Rare:97 | ||||
chr14:50312153-50312374 | Rare:96 | ||||
chr14:50532494-50532606 | Common:2; Rare:36 | ||||
chr14:50668295-50668556 | Common:3; Rare:95 | ||||
chr14:50944390-50944573 | Common:4; Rare:65; Clinvar:1; Clinvar (benign):2 | ||||
chr14:51240102-51240305 | Common:1; Rare:87 | ||||
chr14:51554371-51554769 | Common:1; Rare:89 | ||||
chr14:51651613-51652001 | Common:4; Rare:107 | ||||
chr14:51652010-51652163 | Common:2; Rare:38 | ||||
chr14:52695518-52695809 | Common:1; Rare:77 | ||||
chr14:52707045-52707249 | Common:1; Rare:91 | ||||
chr14:52791427-52791846 | Common:2; Rare:135 | ||||
chr14:54509603-54509929 | Common:5; Rare:106 | ||||
chr14:55027059-55027320 | Common:2; Rare:69 | ||||
chr14:55051462-55051733 | Rare:116 |