Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:52194386-52194583 | Common:1; Rare:52 | ||||
chr13:76882615-76882663 | Rare:10 | ||||
chr13:110174447-110174751 | Rare:100; Clinvar (benign):3 | ||||
chr13:110192829-110193003 | Common:2; Rare:56; Clinvar:4; Clinvar (pathogenic):1 | ||||
chr13:110307828-110308120 | Common:1; Rare:110 | ||||
chr13:110308510-110308601 | Common:1; Rare:20 | ||||
chr13:110424731-110424996 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
chr13:110503852-110504264 | Common:4; Rare:136; Clinvar:1; Clinvar (benign):4 | ||||
chr14:21017759-21017896 | Common:1; Rare:38 | ||||
chr14:49862636-49863039 | Common:1; Rare:183 | ||||
chr14:61570607-61570663 | Rare:8 | ||||
chr14:61721506-61721772 | Common:1; Rare:54 | ||||
chr14:61751065-61751223 | Rare:41 | ||||
chr14:81219235-81219502 | Rare:58 | ||||
chr14:85533086-85533201 | Common:1; Rare:29 |