chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122713100927131010TC34GENIChomozygous50152504
122713109627131097AAAC16GENIChomozygous50152506
122713112827131129TG28GENIChomozygous50152508
122713151127131512CT25GENIChomozygous50405934
122713156527131566AG20GENIChomozygous50152510
122713216827132169GT22GENIChomozygous50152512
122713226427132265CT34GENIChomozygous50405938
122713273727132738TC28GENIChomozygous50405939
122713343027133431AT23GENIChomozygous50152516
122713359027133591TC19GENIChomozygous50152518
122713416127134162TC25GENIChomozygous50152520
122713470727134708A-15GENIChomozygous50152530
122713474327134750AAAAAGA-------13GENICheterozygous50562423
122713497627134977AG16GENIChomozygous50152537
122713499127134992TC19GENIChomozygous50152539
122713507127135075AACT----20GENIChomozygous50152541
122713508227135087AAACA-----18GENIChomozygous50608316
122713516727135168AG16GENIChomozygous50152547
122713540627135408AT--20GENIChomozygous50152549
122713665827136659GA35GENIChomozygous50152551
122713670527136706TC35GENIChomozygous50152553
122713792127137922CCA31GENIChomozygous50152563
122713841027138411TTTGTGTGTGTGTGTGTGTGTGTG7GENIChomozygous50608317
122713886727138868CT25GENIChomozygous50152569
122713913527139136AC16GENIChomozygous50301479
122713913727139138TC17GENIChomozygous50301481
122713914127139142CCGCACGAAT17GENIChomozygous50608318
122714012527140126CT21GENICpossibly homozygous50152573
122714019027140191AC18GENIChomozygous50152575
122714082427140825GGGTGTGT14GENIChomozygous50608319
122714087527140876TC15GENIChomozygous50152583
122714135327141354TC24GENIChomozygous50152585
122714176927141773AAAA----10GENIChomozygous50152587
122714294827142949T-16GENIChomozygous50152593
122714329027143291AG34GENIChomozygous50152595
122714381927143820CT19GENIChomozygous50152599