chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71190506111905062TG20GENIChomozygous53789654
71190557111905572CT34GENIChomozygous53789655
71190564811905649GA26GENIChomozygous53789656
71190578411905785GA24GENIChomozygous53789657
71190618611906187TA11GENIChomozygous53789658
71190618911906190AAGG10GENIChomozygous53789659
71190753711907538AG41GENIChomozygous53789660
71190806911908070AG39GENIChomozygous53789661
71190871211908713GA6GENIChomozygous53789662
71190901711909018AT25GENIChomozygous53789663
71190922711909229TT--15GENICheterozygous53789664
71190922811909229T-15GENICheterozygous53789665
71190961711909618TC4GENIChomozygous53789666
71190965911909660TC4GENICheterozygous54181702
71191047611910477AG28GENIChomozygous53789668
71191050811910509CT41GENIChomozygous53789669
71191051911910520CT39GENIChomozygous53789670
71191061711910618GT34GENIChomozygous53789671
71191093811910939AG16GENIChomozygous53789672
71191134511911346TA30GENIChomozygous53789673
71191295111912952CT38GENIChomozygous53789674
71191310711913108GC38GENIChomozygous53789675
71191379111913792CT44GENIChomozygous53789676
71191399511913996GC49GENIChomozygous53789677