chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6137712276137712277TC73GENIChomozygous114997559
6137712441137712442TG56GENIChomozygous114997560
6137713745137713746GA55GENIChomozygous114997561
6137714202137714203AG73GENIChomozygous114997563
6137714400137714401CT44GENIChomozygous114997564
6137716129137716130AG53GENIChomozygous114997565
6137718815137718816GA78GENICpossibly homozygous114997566
6137719199137719200AG66GENIChomozygous114997567
6137719685137719686TC52GENIChomozygous114997568
6137721764137721765CT50GENIChomozygous114997569
6137721910137721911TC42GENIChomozygous114997570
6137722235137722236AG52GENIChomozygous114997571
6137722344137722345CT49GENIChomozygous114997572
6137725090137725091CT53GENIChomozygous114997573
6137726909137726910CT51GENICpossibly homozygous114997574
6137727023137727024TC23GENIChomozygous114997575
6137727236137727237CT65GENIChomozygous114997576
6137727947137727948CG17GENIChomozygous114997577
6137728086137728087TC49GENIChomozygous114997578
6137729157137729159GC57GENIChomozygous128401517
6137729141137729143GG58GENIChomozygous128401516
6137729163137729165TG56GENIChomozygous128401518
6137729180137729182AG52GENIChomozygous128401519
6137730206137730207TC71GENIChomozygous114997579
6137730875137730876AC54GENIChomozygous114997580
6137732406137732407G31GENIChomozygous128401520