chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4187427652187427653TC10GENIChomozygous57564596
4187427666187427667GA13GENIChomozygous57564598
4187427732187427733GA10GENIChomozygous57564600
4187427999187428000AG31GENIChomozygous57564602
4187428606187428607CT35GENIChomozygous57564604
4187428856187428857TTG34GENIChomozygous57564606
4187428966187428967TC39GENIChomozygous57564608
4187429402187429403GA23GENIChomozygous57564610
4187429738187429739TC38GENIChomozygous57564612
4187430190187430191CT24GENIChomozygous57564614
4187430371187430372CT23GENIChomozygous57564616
4187430382187430383AG19GENIChomozygous57564618
4187430445187430446A-20GENIChomozygous57564620
4187430482187430484GA--28GENIChomozygous57564622
4187430504187430505AG15GENIChomozygous57564624
4187430773187430774AC36GENIChomozygous57564626
4187430978187430979TG43GENIChomozygous57564628
4187431150187431151GA42GENIChomozygous57564630
4187431632187431633GA33GENIChomozygous57564632
4187431731187431732TG23GENIChomozygous57564634
4187431925187431926TG38GENIChomozygous57564636
4187432504187432517TGGGTAGAGGAAG-------------27GENIChomozygous57564638
4187432970187432971TA37GENIChomozygous57564640
4187433184187433185CT35GENIChomozygous57564642
4187433315187433316AG37GENICpossibly homozygous57564644
4187433355187433356CT45GENIChomozygous57564646
4187433610187433611AG21GENICpossibly homozygous57564648
4187433943187433944AG32GENIChomozygous57564650
4187434002187434003AG34GENIChomozygous57564652
4187434244187434245CA37GENIChomozygous57564654
4187434412187434413GA33GENIChomozygous57564656
4187434555187434556CT23GENIChomozygous57564658
4187435477187435478TC34GENIChomozygous57564660
4187435569187435570CCAG34GENIChomozygous57564662
4187435655187435656GC28GENIChomozygous57564664