Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:48303674-48303990 | Common:1; Rare:108; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr13:48975674-48975937 | Common:2; Rare:82 | ||||
chr13:48976414-48976629 | Common:3; Rare:78 | ||||
chr13:49110289-49110386 | Common:1; Rare:28 | ||||
chr13:49247830-49247976 | Rare:45 | ||||
chr13:49443997-49444448 | Common:1; Rare:142 | ||||
chr13:49495791-49496041 | Rare:58 | ||||
chr13:49585520-49585612 | Common:1; Rare:29 | ||||
chr13:49936231-49936569 | Common:1; Rare:104 | ||||
chr13:49997063-49997121 | Rare:22 | ||||
chr13:50081943-50082262 | Common:1; Rare:89 | ||||
chr13:51804102-51804305 | Common:2; Rare:59 | ||||
chr13:52455327-52455507 | Common:3; Rare:59 | ||||
chr13:52652537-52652855 | Common:3; Rare:81 | ||||
chr13:60163869-60164118 | Common:1; Rare:64 |