chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1183695702183695703GA23GENIChomozygous108442841
1183698245183698246AG29GENIChomozygous108442845
1183698991183698992TC35GENIChomozygous108442851
1183699043183699044CA31GENIChomozygous108971637
1183699324183699325GC25GENIChomozygous108971638
1183700771183700772TG21GENIChomozygous108971639
1183701357183701358GT35GENIChomozygous108442853
1183702782183702783TC31GENIChomozygous108442855
1183703318183703319TC27GENIChomozygous108442857
1183704026183704027GA27GENIChomozygous108442859
1183704399183704400AG26GENIChomozygous108442865
1183705290183705291TA29GENIChomozygous108971641
1183705504183705505CT23GENIChomozygous108442869
1183707657183707658GA25GENIChomozygous108971642
1183709204183709205AG24GENIChomozygous108442881
1183709626183709627AG27GENIChomozygous108971643
1183713026183713027GA23GENICheterozygous120509584
1183713027183713028TA22GENICheterozygous120509585
1183713517183713518GA31GENIChomozygous108442887
1183713797183713798AG24GENIChomozygous108442889
1183714075183714076AT25GENIChomozygous108442891
1183715495183715496TC22GENIChomozygous108442893
1183716013183716014TG14GENIChomozygous108971644
1183725108183725109CG21GENIChomozygous108971647
1183717752183717753TC22GENIChomozygous108442897
1183720008183720009TC26GENIChomozygous108442901
1183722748183722749CT23GENIChomozygous108442905
1183725265183725266TC25GENIChomozygous108442907
1183725298183725299CA26GENIChomozygous108971648
1183725380183725381CT20GENIChomozygous108971649
1183726110183726111GA27GENIChomozygous108971650
1183727512183727513CT18GENIChomozygous108442911
1183728122183728123GA19GENIChomozygous108442915