chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157581578157581579GC21GENIChomozygous141670823
4157582017157582018GA14GENIChomozygous141670824
4157582061157582062TA10GENIChomozygous137248653
4157582423157582424CT9GENIChomozygous141670825
4157583016157583017AG17GENIChomozygous137248654
4157583118157583132CGTGTGTGCGAGCA15GENIChomozygous136925236
4157583208157583209GC18GENIChomozygous137248655
4157583545157583545G20GENIChomozygous136925237
4157584473157584474GA27GENIChomozygous141670826
4157584935157584936C12GENIChomozygous136925238
4157585132157585133A16GENIChomozygous136925239
4157587516157587517AG25GENIChomozygous137248662
4157589246157589247GA20GENIChomozygous137248664
4157589318157589319TC21GENIChomozygous137248665
4157589352157589353TA22GENIChomozygous137248666
4157589458157589459GT23GENIChomozygous137248667
4157591360157591361GA23GENIChomozygous137248668
4157591410157591411GA25GENIChomozygous141670827
4157583586157583606TCCTTCCTTCCTTCCTTCCC18GENIChomozygous141589303
4157583604157583605C18GENIChomozygous403125155
4157583604157583605CT18GENICheterozygous154220550