chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4171069422171069423CT14GENIChomozygous112951590
4171069650171069651CT21GENIChomozygous112951592
4171069888171069889TC21GENIChomozygous112951596
4171070067171070068CA22GENIChomozygous112951598
4171070103171070104AC24GENIChomozygous112951601
4171070262171070263CG13GENIChomozygous112951603
4171071372171071373TA10GENIChomozygous112951605
4171071485171071486AG4GENIChomozygous112951607
4171073451171073452AG6GENIChomozygous112951609
4171074429171074430AG22GENIChomozygous112951611
4171075586171075587AT18GENIChomozygous112951613
4171077326171077327GT16GENIChomozygous112951615
4171086266171086267GT28GENIChomozygous112951621
4171086914171086915TA16GENIChomozygous112951625
4171087143171087144TC12GENIChomozygous112951627
4171087491171087492CT13GENIChomozygous112951629
4171091249171091250GA24GENIChomozygous112951635
4171091582171091583AG32GENIChomozygous112951637
4171091912171091913CA34GENIChomozygous112951639
4171092570171092571CT21GENIChomozygous112951641
4171097108171097109GT18GENIChomozygous112951647
4171098502171098503AT3GENIChomozygous119565315
4171098704171098705AC15GENIChomozygous112951649
4171142198171142199GA16GENIChomozygous112951651
4171142474171142475GC10GENIChomozygous112951653