chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1183695702183695703GA30GENIChomozygous108442841
1183696023183696024CT37GENIChomozygous108442843
1183698245183698246AG18GENIChomozygous108442845
1183701357183701358GT27GENIChomozygous108442853
1183702782183702783TC46GENIChomozygous108442855
1183703318183703319TC28GENIChomozygous108442857
1183704026183704027GA51GENIChomozygous108442859
1183704288183704289TA26GENICpossibly homozygous108442861
1183704299183704300CT24GENIChomozygous108442863
1183704399183704400AG21GENIChomozygous108442865
1183705504183705505CT26GENIChomozygous108442869
1183705529183705530CT28GENIChomozygous108442871
1183707087183707088GT35GENIChomozygous108442873
1183707664183707665CT45GENIChomozygous108442875
1183708128183708129CT21GENIChomozygous108442877
1183708630183708631AG29GENIChomozygous108442879
1183709204183709205AG30GENIChomozygous108442881
1183709574183709575CT15GENIChomozygous108442883
1183711739183711740GA41GENIChomozygous108442885
1183713517183713518GA14GENIChomozygous108442887
1183713797183713798AG8GENIChomozygous108442889
1183714075183714076AT16GENIChomozygous108442891
1183715495183715496TC43GENIChomozygous108442893
1183715823183715824GA26GENIChomozygous108442895
1183717752183717753TC43GENIChomozygous108442897
1183719495183719496TC34GENIChomozygous108442899
1183720008183720009TC33GENIChomozygous108442901
1183722380183722381CA56GENICpossibly homozygous108442903
1183722748183722749CT40GENIChomozygous108442905
1183725265183725266TC47GENIChomozygous108442907
1183726358183726359TC46GENIChomozygous108442909
1183727512183727513CT55GENIChomozygous108442911
1183727590183727591GA58GENIChomozygous108442913
1183728122183728123GA25GENIChomozygous108442915