chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95308559153085592CT37GENIChomozygous976404478
95308763053087631TC29GENIChomozygous976404479
95308968253089683GA24GENIChomozygous976404480
95308995553089956AC22GENIChomozygous976404481
95309010153090102CT19GENIChomozygous976404482
95309079753090798GT10GENIChomozygous976404483
95309084553090846GA9GENIChomozygous976404484
95309142953091430GA31GENIChomozygous976404485
95309166253091663CT33GENIChomozygous976404486
95309201053092011GT22GENIChomozygous976404487
95309575253095753TA27GENIChomozygous976404488
95309658153096582TC21GENICpossibly homozygous976404489