chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
65123199851231999GT22GENIChomozygous115110693
65123251651232517GA11GENIChomozygous118807286
65123291751232918GA24GENIChomozygous114798734
65123328951233290TC17GENIChomozygous115110695
65123362351233624TA24GENIChomozygous114798735
65123392951233930AG5GENIChomozygous126415559
65123407351234074CT24GENIChomozygous115110696
65123443451234435CT26GENIChomozygous115110697
65123446151234462TC24GENIChomozygous114798737
65123468951234690GA27GENIChomozygous115110699
65123514451235145TG19GENIChomozygous115110700
65123590151235902AG10GENIChomozygous115110701
65123619751236198TC21GENIChomozygous115110702
65123655151236552CT11GENIChomozygous115110703
65123821551238216GA13GENIChomozygous115110705
65123861451238615GA15GENIChomozygous115110706
65123969651239697CT18GENIChomozygous115110708
65124033751240338GA14GENIChomozygous114798738
65124046451240465CT15GENIChomozygous118609483
65124173751241738TC17GENIChomozygous114798739
65124555051245551TC25GENIChomozygous118609484
65124574451245745AG31GENIChomozygous114798743
65124752751247528GA26GENIChomozygous114798747
65124874551248746GA16GENIChomozygous118609486
65125144251251443TA6GENIChomozygous115110714
65125246751252468TA23GENIChomozygous115110715
65125324951253250AC11GENIChomozygous115110716
65125332151253322CT3GENICheterozygous118661070
65125452851254529AG15GENIChomozygous115110717
65125516651255167GA12GENIChomozygous115110719
65125539751255398CT24GENIChomozygous115110720
65125342751253428CT9GENICheterozygous126448690