chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122698070926980710A-7GENICheterozygous50151323
122698704026987041GT10GENIChomozygous50539503
122698848026988481AATCTC2GENIChomozygous50539504
122699071126990712AAACACAC8GENIChomozygous50509491
122699124126991242T-3GENICheterozygous50301067
122699226326992264TTA4GENICheterozygous50557851
122700167927001681AC--10GENICheterozygous50600636
122701327027013271TC8GENIChomozygous50419773
122701334627013347TA12GENIChomozygous50373835
122701362827013629AG7GENIChomozygous50373837
122701362927013630CCT7GENIChomozygous50373839
122701369827013699CCAAAAAAAAAAAAAAAA2GENIChomozygous50509499
122701389127013892AAAC5GENIChomozygous50373844
122701391827013919GA7GENIChomozygous50373846
122701409627014097GA3GENIChomozygous50373848
122701429527014296GA2GENIChomozygous50373850
122701441127014415TACC----8GENIChomozygous50373852
122701444727014448GA9GENIChomozygous50373854
122701454727014548AG8GENIChomozygous50373856
122701478727014788CT10GENIChomozygous50373858
122701508827015089CT7GENIChomozygous50373860
122701534127015342TC9GENIChomozygous50373862
122701554327015545CA--2GENIChomozygous50373864
122701556027015562AT--9GENIChomozygous50151556
122701559227015598ACACAT------5GENICheterozygous50509501
122701562227015623CT10GENIChomozygous50373866
122701588127015882GA3GENIChomozygous50373868
122701592327015926AAC---10GENIChomozygous50373870
122701621827016219TC14GENIChomozygous50373888
122701624027016241AG12GENIChomozygous50301121
122701635127016352GA7GENIChomozygous50373890
122701669227016699AAAAAAA-------4GENIChomozygous50373892
122701684627016847GA7GENIChomozygous50467375
122701695327016971GGAGGACTTGGTGGGCCC------------------7GENIChomozygous50509506
122701699527016996CT7GENIChomozygous50373900
122701701227017013AT10GENIChomozygous50373902
122701769327017694TTA7GENIChomozygous50151560
122701787527017876TC6GENIChomozygous50151562
122702134527021346TTGAAG2GENIChomozygous50301125
122702233027022331GT4GENIChomozygous50301131