chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205270043205270044TA30GENIChomozygous61064510
1205271430205271431AG17GENIChomozygous61064511
1205272354205272355G-22GENICheterozygous61064512
1205272361205272362G-23GENICheterozygous61064513
1205272362205272364AA--20GENICheterozygous61318287
1205272526205272527T-19GENIChomozygous61064514
1205272555205272556AC23GENIChomozygous61064515
1205273128205273129CCA18GENICheterozygous62361659
1205273130205273131A-18GENICheterozygous61585541
1205274336205274341GGTTC-----8GENICheterozygous62095826
1205274419205274420C-6GENICheterozygous62301615
1205275621205275622T-10GENIChomozygous61064516
1205275862205275863CA15GENIChomozygous61064517
1205275986205275987GA14GENIChomozygous61064518
1205276398205276399AAC14GENICheterozygous61064519
1205276583205276584CT20GENIChomozygous61064520
1205277189205277192TTT---8GENICpossibly homozygous61064521
1205277421205277422A-17GENIChomozygous61064522
1205278192205278194CT--22GENIChomozygous61064523
1205278201205278202TA28GENICpossibly homozygous61585547