chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2086644228664423GA35GENIChomozygous130044182
2086644758664476GA30GENIChomozygous130044185
2086654888665488AG32GENIChomozygous129981604
2086658998665900AG40GENIChomozygous130044187
2086673538667354GA58GENIChomozygous130044190
2086678138667814AG47GENIChomozygous130044193
2086678578667858AG45GENIChomozygous130044196
2086680878668088C8GENIChomozygous129981605
2086685718668572TC39GENIChomozygous130044199
2086695098669510AG47GENIChomozygous130044202
2086709418670947GGGGGA14GENICheterozygous144499998
2086717278671728TC49GENIChomozygous130044205
2086726368672639GGG62GENIChomozygous129981606
2086726408672640ATTTA62GENIChomozygous129981607
2086728208672821GA49GENIChomozygous130044207
2086728448672845CA50GENIChomozygous130044210
2086729178672918CT67GENIChomozygous130044213
2086756228675623GA51GENIChomozygous130044216
2086771408677140TGC33GENIChomozygous129981608
2086771428677144GG33GENIChomozygous129981609
2086771468677146GGGCCTCAGGGC33GENIChomozygous129981610
2086771518677151TTGTGGTCTG33GENIChomozygous129981611
2086771518677152AG33GENIChomozygous130044219
2086771558677156AG33GENIChomozygous130044222
2086771598677160AG46GENIChomozygous130044225
2086775738677574C50GENIChomozygous129981612
2086776348677635GA40GENIChomozygous130044228
2086780378678038CT64GENIChomozygous130044231
2086781858678185AG30GENIChomozygous129981613
2086783668678367TC37GENIChomozygous130044234
2086784958678496TG43GENIChomozygous130044237
2086791578679158TC59GENICpossibly homozygous130044240
2086804748680474A54GENIChomozygous129981614
2086808388680838CAGCCATGCAGAGGCAGGGACCACACCTGAATGAGTCTTGCCTATTCTAAGTA4GENIChomozygous129981615
2086709308670931GA19GENIChomozygous403463392
2086680878668088CT8GENICheterozygous403463390
2086709308670931G19GENICheterozygous403463391