Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:42271453-42271512 | Rare:18 | ||||
chr13:52194402-52194510 | Rare:32 | ||||
chr13:52617425-52617531 | Rare:22 | ||||
chr13:75365835-75366107 | Common:1; Rare:43 | ||||
chr13:75366975-75367136 | Common:3; Rare:31 | ||||
chr13:95083823-95083942 | Common:2; Rare:14 | ||||
chr13:106376445-106376625 | Common:1; Rare:35 | ||||
chr13:110870196-110870542 | Common:3; Rare:55 | ||||
chr14:38254565-38254815 | Rare:88 | ||||
chr14:38255405-38255561 | Rare:60 | ||||
chr14:49633941-49634070 | Common:1; Rare:53; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49862655-49863025 | Common:1; Rare:172 | ||||
chr14:72665540-72665677 | Common:1; Rare:21 | ||||
chr14:73245979-73246082 | Common:2; Rare:37 | ||||
chr14:81219361-81219502 | Rare:29 |