chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
21359363713593638TC13GENIChomozygous109610032
21359408213594083AC25GENIChomozygous111087983
21359608613596087TC15GENIChomozygous111087985
21359636113596362TC11GENIChomozygous111087987
21359684213596843GA18GENIChomozygous111087989
21359725913597260AC14GENIChomozygous111087991
21359755813597559AG23GENIChomozygous111087993
21359987913599880TG26GENIChomozygous111087996
21360010013600101GA24GENIChomozygous109610052
21360068713600688TC20GENIChomozygous109610056
21360127913601280GA20GENIChomozygous111087998
21360131913601320CT18GENIChomozygous109610057
21360169213601693GA17GENIChomozygous111088000
21360170213601703CT16GENIChomozygous109610058
21360325213603253AT8GENIChomozygous111088002
21360356213603563AG11GENIChomozygous111088004
21360383913603840CT17GENIChomozygous109610062
21360394113603942AT14GENIChomozygous109610063
21360444013604441AG15GENIChomozygous109610065
21360515013605151AG12GENIChomozygous109610070
21360532913605330AG15GENIChomozygous109610071
21360538313605384AG18GENIChomozygous111088006
21360701913607020AG15GENIChomozygous111088008
21360858913608590GA21GENIChomozygous111088010
21360913013609131CG25GENIChomozygous109610078
21360923013609231GT23GENIChomozygous109610079
21360950713609508AG12GENIChomozygous109610081
21361198213611983TC20GENIChomozygous111088015
21361293913612940TC22GENIChomozygous109610087
21361349513613496TC17GENIChomozygous109610090
21361364713613648TC22GENIChomozygous109610091
21361043613610440AGGG9GENIChomozygous130858067