chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46860492668604927AG29GENIChomozygous112691659
46860550868605509CT63GENIChomozygous112691661
46860724168607242AT38GENIChomozygous112691663
46860841368608414AC44GENIChomozygous112691665
46861180868611809TA34GENIChomozygous112691667
46861209968612100TG23GENIChomozygous112691669
46861212568612126GA31GENIChomozygous112691671
46861281668612817TA35GENIChomozygous112691673
46861345968613460CG37GENIChomozygous112691675
46861401068614011AG55GENIChomozygous112691677
46861438868614389CT51GENICpossibly homozygous112691679
46861621768616218CT34GENIChomozygous112691681
46861654368616544GT30GENIChomozygous112691685
46862163268621633GT41GENIChomozygous112691687
46862209868622099TC24GENIChomozygous112691689
46862250268622503AG21GENIChomozygous112691691
46862272868622729TC19GENIChomozygous112691693
46862290168622902GT34GENIChomozygous112691695
46862297868622979CT37GENIChomozygous112691697
46862324868623249GA57GENIChomozygous112691699
46862540168625402CA26GENIChomozygous112691701