chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174347347043473471CT8GENIChomozygous891030578
174347361743473618GA8GENIChomozygous891030579
174347385843473859CT25GENIChomozygous891030580
174347450543474506CT18GENIChomozygous891030581
174347473343474734GT16GENIChomozygous891030582
174347488943474890GC23GENIChomozygous891030583
174347567843475679GA7GENIChomozygous891030584
174347643643476437TC13GENIChomozygous891030585
174347729343477294GC13GENIChomozygous891030586
174347745243477453GT14GENIChomozygous891030587
174347912343479124CT19GENIChomozygous891030588
174347929843479299GA27GENIChomozygous891030589
174347996843479969TA12GENIChomozygous891030590
174348081943480820AG6GENIChomozygous891030591
174348152543481526CA17GENIChomozygous891030592
174348200443482005CT8GENIChomozygous891030593
174348205543482056AC10GENIChomozygous891030594
174348253543482536TC22GENIChomozygous891030595
174348439043484391CG29GENIChomozygous891030596
174348829343488294TC4GENICheterozygous891030598
174348860243488603CG11GENICheterozygous891030599
174348863043488631TC10GENICheterozygous891030600
174349012843490129GC5GENICheterozygous891030601
174349082843490829GC8GENIChomozygous891030602
174349099843490999TC19GENIChomozygous891030603
174349114343491144GT12GENIChomozygous891030604
174349189243491893GT14GENIChomozygous891030605
174349213643492137GA5GENIChomozygous891030606
174349275543492756TC4GENICheterozygous891030597