chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85280356452803565CT59GENIChomozygous117941488
85280362852803629CT58GENIChomozygous116963411
85280493752804938AG50GENIChomozygous116963412
85280543252805433GA43GENIChomozygous117941489
85280560552805606CT54GENIChomozygous117941490
85280586052805861AG71GENIChomozygous117941491
85280786952807870TA64GENIChomozygous116818483
85280810852808109TC35GENIChomozygous116818485
85280817752808178CA35GENIChomozygous117941492
85280855652808557AG56GENIChomozygous116818487
85280858152808582TC55GENIChomozygous116818489
85280860552808606TG54GENIChomozygous117941493
85280893752808937G53GENIChomozygous130362193
85280905852809059CA52GENIChomozygous116963415
85280944652809447AT18GENIChomozygous118077193
85280964652809647GA58GENIChomozygous116963416
85280981752809818AT55GENIChomozygous116818491
85281035452810372GTGTGTGTGTGCGCGCGC21GENIChomozygous133188981
85281134452811345TG61GENIChomozygous116818495
85281185452811855TC77GENIChomozygous116818501
85281219052812191AG54GENIChomozygous116963418
85281274452812744TG58GENICpossibly homozygous130362194
85281275852812758TG57GENICpossibly homozygous130362195
85280944352809445AA14GENIChomozygous128590776
85281022752810227TTCCTAAACTTTATT52GENIChomozygous128590777
85280945352809454AT17GENIChomozygous128660612
85280945452809455AT18GENIChomozygous128660613
85280945552809456AT19GENIChomozygous128660614
85280963052809638GCCACAGA58GENIChomozygous132666647