chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75846351258463516TCTC----28GENICheterozygous54420586
75846351458463516TC--28GENICpossibly homozygous53930141
75846398958463990TG33GENICheterozygous54420590
75847002058470021A-16GENICheterozygous54826267
75847450558474508CCC---14GENICheterozygous53930145
75847450758474508C-14GENICheterozygous53930147
75848871258488716AAAA----19GENICheterozygous54826269
75848871558488716A-19GENICheterozygous53930149
75848993158489932C-20GENICheterozygous53930151
75850632558506326GGT21GENICheterozygous54420611
75851524958515250AG103GENICheterozygous53930153
75851558658515587TTG1GENIChomozygous54196060
75851561558515616TG15GENICheterozygous54196062
75851727958517280AC17GENICheterozygous53930157
75852866358528664CT39GENIChomozygous53930161
75852917958529183ACAC----18GENICheterozygous53930163
75852923058529231TA34GENIChomozygous53930164
75853438658534387CT29GENICheterozygous53930166
75853629158536292CCT23GENICheterozygous54196065
75853629258536293T-23GENICheterozygous54196066
75853634358536344GGA34GENIChomozygous54826271
75854390358543904GC31GENIChomozygous53930168
75854405758544058C-19GENIChomozygous53930170
75854408558544086C-23GENICheterozygous54420636
75854513158545132GGT19GENIChomozygous53930172
75855640358556404AAG4GENIChomozygous53930173
75856099558560996AT42GENIChomozygous54826273
75856242558562426TTAC43GENIChomozygous53930175
75856251758562521ACAC----6GENIChomozygous54420638
75857059458570595AAT37GENIChomozygous53930179
75857093358570934G-29GENIChomozygous53930181
75857269058572691GT35GENICheterozygous53930183
75858849258588493T-25GENIChomozygous53930185
75858853858588539TTA36GENIChomozygous53930187
75858873958588740G-47GENIChomozygous53930189
75858888458588885AATG20GENICpossibly homozygous53930190
75858940958589410GC11GENIChomozygous54196069
75859240158592405AAAA----25GENICheterozygous54736116
75859240458592405A-25GENICheterozygous53930192