chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
67617453776174538AG36GENIChomozygous114862602
67617587176175872GA60GENIChomozygous114862603
67617822676178227GA45GENIChomozygous114862604
67617911876179119AC37GENIChomozygous118630025
67617581676175817CT62GENIChomozygous115258542
67618004476180045CT45GENIChomozygous115258544
67617590376175903A60GENIChomozygous128355537
67618366176183662TA54GENIChomozygous114862605
67618531876185319AG47GENIChomozygous114862606
67619042276190423TC52GENIChomozygous114862607
67619165676191657TC8GENIChomozygous114862608
67619203076192031CA28GENIChomozygous114862609
67619284976192850TC42GENIChomozygous114862610
67619485176194852TA52GENIChomozygous114862612
67619606076196061GA40GENIChomozygous114862613
67619993676199937TC49GENIChomozygous114862614
67620095276200953TC39GENIChomozygous118630026
67620177476201775GA61GENIChomozygous114862615
67620192276201923GA48GENIChomozygous114862616
67620397076203971AG42GENIChomozygous114862617
67617645076176450GTGA33GENIChomozygous128355538
67617640776176409TG37GENIChomozygous130981792
67618069176180692T37GENIChomozygous130981793
67619392376193923T39GENIChomozygous128355539
67619586976195870T44GENIChomozygous128355540
67620405676204057AG41GENIChomozygous114862618
67620441776204418GA40GENIChomozygous114862619
67620449876204499TG32GENIChomozygous126353616
67620450476204509TTTTC30GENIChomozygous128355542