chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266783577266783578GA14GENIChomozygous108784199
1266785511266785512GA32GENICpossibly homozygous109028394
1266785751266785752GT28GENIChomozygous108638579
1266786056266786057GA20GENIChomozygous108638580
1266786843266786844GA16GENICpossibly homozygous120516203
1266788634266788635AT32GENIChomozygous108638582
1266789132266789133GA29GENICpossibly homozygous109028395
1266789397266789398AG22GENIChomozygous108638583
1266789856266789857TC24GENIChomozygous108638584
1266790358266790359CA23GENIChomozygous108638585
1266790673266790674GA16GENICpossibly homozygous109028396
1266791552266791553AG23GENIChomozygous108638586
1266792042266792043GA26GENIChomozygous108638588
1266792173266792174TC26GENIChomozygous108638589
1266792260266792261TC19GENIChomozygous108638590
1266792346266792347TC21GENIChomozygous108638591
1266792648266792649AG32GENIChomozygous108638592