chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1278199027278199028GA22GENIChomozygous108662181
1278199627278199628GA19GENIChomozygous108662182
1278199849278199850CT14GENIChomozygous120896276
1278200469278200470CG18GENIChomozygous120477697
1278200670278200671GA22GENIChomozygous108662183
1278201249278201250CA20GENIChomozygous108662184
1278201707278201708TG23GENIChomozygous120896277
1278201951278201952AG18GENIChomozygous108662186
1278202042278202043AG17GENIChomozygous108662187
1278202344278202345CT20GENIChomozygous108662188
1278202386278202387AT25GENIChomozygous108662189
1278202658278202659AT17GENIChomozygous120896278
1278202714278202715TC17GENIChomozygous108662191
1278202937278202938TC9GENIChomozygous108662192
1278203704278203705TC18GENIChomozygous109034021
1278204344278204345AC15GENIChomozygous108662196
1278204899278204900TA20GENIChomozygous108662201
1278205172278205173CA22GENIChomozygous120697767
1278205825278205826AG16GENIChomozygous108662203
1278205857278205858GT14GENIChomozygous108662204
1278205859278205860GT14GENIChomozygous108662205
1278206422278206423TC15GENIChomozygous108662207
1278207082278207083CG23GENIChomozygous108662210
1278207299278207300TG27GENIChomozygous108662213
1278208104278208105TA18GENIChomozygous108662216
1278200471278200472TC17GENIChomozygous109221217
1278209627278209628TC22GENIChomozygous108662221
1278212102278212103AG22GENIChomozygous108662232
1278212522278212523CT15GENIChomozygous120896279
1278214784278214785GA12GENIChomozygous120896280
1278218715278218716TC12GENIChomozygous120896281
1278218824278218825CT16GENIChomozygous108806918
1278219866278219867AG17GENIChomozygous120896282
1278222679278222680AC11GENIChomozygous108662270
1278224181278224182TC16GENIChomozygous108662278