chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112428661112428662AG18GENIChomozygous934666066
3112442079112442080AG28GENIChomozygous934666067
3112447995112447996CT30GENIChomozygous934666068
3112448948112448949CT21GENIChomozygous934666069
3112449836112449837GA19GENIChomozygous934666070
3112451798112451799GA32GENIChomozygous934666071
3112452566112452567TC41GENIChomozygous934666072
3112456160112456161CG33GENIChomozygous934666073
3112456481112456482AT23GENIChomozygous934666074
3112457081112457082CA12GENIChomozygous934666075
3112458853112458854CG26GENIChomozygous934666076
3112464930112464931TC8GENIChomozygous934666077
3112467917112467918GA32GENIChomozygous934666078
3112475176112475177AG26GENIChomozygous934666079
3112479306112479307CT33GENIChomozygous934666080
3112483051112483052AT31GENIChomozygous934666081
3112485432112485433TG31GENIChomozygous934666082
3112487752112487753CT20GENIChomozygous934666083
3112490378112490379AC28GENIChomozygous934666084
3112490615112490616TC34GENIChomozygous934666085
3112492204112492205CT21GENIChomozygous934666086
3112492776112492777CA21GENIChomozygous934666087
3112495656112495657CT16GENIChomozygous934666088
3112498199112498200AG22GENIChomozygous934666089
3112502306112502307AC14GENICheterozygous934666090
3112502449112502450AG14GENIChomozygous934666091
3112503398112503399AG25GENIChomozygous934666092
3112505307112505308CT28GENIChomozygous934666093
3112505352112505353TC26GENIChomozygous934666094
3112506333112506334GT24GENIChomozygous934666095
3112507325112507326GC29GENIChomozygous934666096
3112655241112655242GA40INTERGENIChomozygous934666097
3112655546112655547TA33INTERGENIChomozygous934666098
3112656277112656278TC30INTERGENIChomozygous934666099
3112657145112657146TC23INTERGENIChomozygous934666100
3112657638112657639TC34INTERGENIChomozygous934666101
3112658211112658212GA26INTERGENIChomozygous934666102
3112658758112658759GA22INTERGENIChomozygous934666103