chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1534345123434513A-4GENICheterozygous48223854
1534451793445183CACA----15GENICheterozygous49184637
1534451813445183CA--15GENICheterozygous49184639
1534491123449113CA9GENIChomozygous48223857
1534491153449116CG9GENIChomozygous48223858
1534515413451542CT34GENIChomozygous48223863
1534515423451543TC34GENIChomozygous48223864
1534517773451778C-21GENIChomozygous48223865
1534517793451780AAC23GENIChomozygous48223866
1534733553473361GTGTGT------3GENICheterozygous49025717
1534733573473361GTGT----3GENICheterozygous49025719
1534900713490072AT34GENIChomozygous48223873
1534929373492938CCA21GENICheterozygous49141681
1534957163495717GGT5GENICheterozygous49079023
1534978213497822A-2GENIChomozygous49184642
1534987313498733CA--19GENICheterozygous49025771
1535019043501905TTATA3GENIChomozygous48223875
1535091243509125A-7GENIChomozygous48223876
1535091303509131AAG7GENIChomozygous48223877
1535091393509140AG6GENIChomozygous49079028
1535091413509142TA6GENIChomozygous49079030
1535115653511566A-13GENICheterozygous49079032
1535121793512209ATGATTTCTGTTTAAATATCCTAGCATTGA------------------------------23GENICheterozygous49079035
1535122123512216CAAT----13GENICheterozygous49079037
1535122193512222CAA---10GENICheterozygous49079039
1535161213516125GGAC----10GENICheterozygous49079042
1535161223516123GC10GENICpossibly homozygous48223880
1535163243516325C-32GENIChomozygous48223881
1535181303518131GGT2GENICheterozygous49025806
1535181363518139TTT---2GENICheterozygous49079044
1535221813522182AC6GENIChomozygous48223882
1535221823522183CA6GENIChomozygous48451909
1534929383492939A-21GENICheterozygous48737893