Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:67660227-67660365 | Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
chr16:67666699-67666862 | Rare:34 | ||||
chr16:67843650-67843953 | Rare:47 | ||||
chr16:68023212-68023323 | Common:1; Rare:28 | ||||
chr16:68310931-68311107 | Common:1; Rare:89 | ||||
chr16:69132532-69132682 | Rare:61 | ||||
chr16:69330554-69330784 | Common:2; Rare:99 | ||||
chr16:69339510-69339826 | Common:1; Rare:140; Clinvar:1; Clinvar (benign):3 | ||||
chr16:69339877-69339909 | Rare:12 | ||||
chr16:69424487-69424698 | Common:1; Rare:64 | ||||
chr16:69726444-69726726 | Common:3; Rare:75 | ||||
chr16:70346759-70346945 | Common:1; Rare:91 | ||||
chr16:70523494-70523847 | Common:3; Rare:125; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr16:71809042-71809129 | Rare:39 | ||||
chr16:71895216-71895559 | Common:2; Rare:134 |