chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5142911567142911568CT11GENIChomozygous114253283
5142913112142913113GA16GENICpossibly homozygous114253285
5142915372142915372C15GENIChomozygous131651139
5142915512142915513TC6GENIChomozygous114034015
5142915654142915655CA15GENICheterozygous114253289
5142915694142915695AC10GENICheterozygous131657916
5142915698142915699GA10GENICheterozygous131657917
5142919223142919224AG2GENIChomozygous128301450
5142919562142919563AG3GENICheterozygous128301451
5142921116142921117CT6GENICheterozygous131657920
5142921864142921865GA17GENIChomozygous114253291
5142924565142924566CT29GENIChomozygous114034019
5142924627142924628AG18GENIChomozygous114253293
5142924884142924885TC23GENIChomozygous114253295
5142924953142924954GA24GENIChomozygous114253297
5142926519142926519AC15GENICheterozygous131651140
5142926562142926563TC17GENIChomozygous114034021
5142926580142926581CT19GENIChomozygous114253299
5142927181142927182CT26GENIChomozygous114034023
5142927265142927266CG20GENIChomozygous114253301
5142927647142927648TC20GENIChomozygous114253303
5142927827142927828AT26GENIChomozygous114253305
5142927977142927978TC11GENIChomozygous114034024
5142928152142928153AT18GENIChomozygous114253307
5142930457142930458AG22GENIChomozygous114253309
5142931662142931663GT18GENIChomozygous114253311
5142931700142931701GA15GENIChomozygous114034026
5142921096142921097GT2GENIChomozygous129923908
5142931913142931914AG14GENIChomozygous114034027
5142932638142932640CT2GENIChomozygous131651141
5142932644142932646CT2GENIChomozygous131651142
5142932665142932665CC2GENIChomozygous131651143
5142932697142932698TG2GENIChomozygous132090065
5142932689142932689C2GENIChomozygous132303267