chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2086644228664423GA43GENIChomozygous130044182
2086644758664476GA37GENIChomozygous130044185
2086654888665488AG41GENIChomozygous129981604
2086658998665900AG39GENIChomozygous130044187
2086673538667354GA43GENIChomozygous130044190
2086678138667814AG45GENIChomozygous130044193
2086678578667858AG50GENIChomozygous130044196
2086680878668088C14GENIChomozygous129981605
2086685718668572TC35GENIChomozygous130044199
2086695098669510AG52GENIChomozygous130044202
2086717278671728TC41GENIChomozygous130044205
2086726368672639GGG53GENIChomozygous129981606
2086726408672640ATTTA53GENIChomozygous129981607
2086728208672821GA42GENIChomozygous130044207
2086728448672845CA46GENIChomozygous130044210
2086729178672918CT61GENIChomozygous130044213
2086771408677140TGC42GENIChomozygous129981608
2086771428677144GG42GENIChomozygous129981609
2086771468677146GGGCCTCAGGGC42GENIChomozygous129981610
2086771518677151TTGTGGTCTG42GENIChomozygous129981611
2086771598677160AG54GENIChomozygous130044225
2086709308670931GA12GENIChomozygous403463392
2086680878668088CT14GENICheterozygous403463390
2086709308670931G12GENICheterozygous403463391
2086709418670947GGGGGA11GENICheterozygous144499998
2086756228675623GA35GENIChomozygous130044216
2086771518677152AG42GENIChomozygous130044219
2086771558677156AG42GENIChomozygous130044222
2086775738677574C47GENIChomozygous129981612
2086776348677635GA44GENIChomozygous130044228
2086780378678038CT31GENIChomozygous130044231
2086781858678185AG38GENIChomozygous129981613
2086783668678367TC45GENIChomozygous130044234
2086784958678496TG48GENIChomozygous130044237
2086791578679158TC50GENIChomozygous130044240
2086804748680474A35GENIChomozygous129981614
2086808388680838CAGCCATGCAGAGGCAGGGACCACACCTGAATGAGTCTTGCCTATTCTAAGTA3GENIChomozygous129981615