chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2233754710233754711CG63GENICpossibly homozygous136508630
2233756134233756135CA55GENIChomozygous136508631
2233757786233757787CT48GENIChomozygous136508632
2233760671233760679TAAGTAAC39GENIChomozygous142907056
2233764740233764741TC64GENIChomozygous136508633
2233764987233764988CT68GENIChomozygous136508634
2233765808233765809AG61GENIChomozygous136508635
2233766155233766156TG48GENIChomozygous136508637
2233767121233767122AT55GENICheterozygous153951695
2233766537233766538CT31GENICheterozygous153951693
2233766541233766542CT32GENICheterozygous153951694
2233766537233766538C31GENIChomozygous403044548
2233766541233766542C32GENIChomozygous403044549
2233767120233767121A54GENICheterozygous403044550
2233767120233767121AT54GENICheterozygous403044551
2233767121233767122A55GENICheterozygous403044552
2233767546233767547CT67GENIChomozygous136508638
2233768808233768809AG69GENIChomozygous136508639
2233770251233770252GA56GENIChomozygous136508640
2233770490233770491GC63GENIChomozygous136508641
2233770871233770872GA50GENIChomozygous136508642
2233770989233770990AG57GENIChomozygous136508643
2233771105233771106TC56GENIChomozygous136508644
2233771583233771584CA68GENICpossibly homozygous136508645
2233772265233772266TC60GENIChomozygous136508646
2233772851233772852GC54GENIChomozygous153951696
2233774087233774088CT65GENIChomozygous136508647
2233775320233775321AG59GENIChomozygous136508648
2233775468233775469AC58GENIChomozygous136508649
2233776066233776067TC53GENIChomozygous136508650
2233777891233777892GA69GENIChomozygous136508651
2233778256233778257CT45GENIChomozygous136508652
2233778678233778678TCCCC24GENICpossibly homozygous135988481
2233770416233770416C57GENIChomozygous135988477
2233772879233772880T43GENICpossibly homozygous135988478
2233773560233773561T66GENIChomozygous135988479
2233774583233774583GGGA65GENIChomozygous135988480
2233772851233772852G54GENICheterozygous403567340
2233783043233783044AC60GENIChomozygous136508653
2233784510233784511CA38GENIChomozygous136508654