chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102850603102850604CT23GENIChomozygous109115159
1102851506102851507CT20GENIChomozygous109115161
1102851644102851644G15GENIChomozygous130818445
1102852270102852271AT27GENIChomozygous109115163
1102854051102854053AT17GENIChomozygous130818446
1102854281102854281T12GENIChomozygous131985265
1102856959102856960AG11GENIChomozygous109115165
1102857517102857518GA24GENIChomozygous109115167
1102857939102857940AC14GENIChomozygous109115169
1102859932102859933GA22GENIChomozygous109115171
1102860307102860308AG21GENIChomozygous109115173
1102860567102860567T15GENIChomozygous130818447
1102861662102861663C10GENIChomozygous130818448
1102863542102863542TCAGGG13GENIChomozygous130818449
1102865656102865657AG13GENIChomozygous109115175
1102867008102867009TC18GENIChomozygous109115177
1102868455102868456CG19GENIChomozygous109115179
1102868636102868637GA11GENIChomozygous109115181
1102868865102868866A12GENIChomozygous130818450
1102870765102870766TC16GENIChomozygous109115183
1102871437102871438TC15GENIChomozygous109115185
1102873418102873419AT11GENICpossibly homozygous109115187
1102873954102873955AG14GENIChomozygous109115189
1102875231102875232AG15GENIChomozygous109115191
1102875241102875242GT14GENIChomozygous109115193
1102875429102875430CT14GENIChomozygous109115195
1102876423102876424AG19GENIChomozygous109115197
1102876799102876800AG11GENIChomozygous109115199
1102877391102877392A12GENIChomozygous130818451
1102877576102877577CT16GENIChomozygous109115201
1102865261102865261T15GENIChomozygous130519484
1102869426102869428AT14GENIChomozygous130731329