chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1160452672160452673TC16GENIChomozygous60916783
1160452911160452912TA27GENIChomozygous60916784
1160453192160453193AAAG23GENIChomozygous61771912
1160453401160453402AATCTTCCTTTGAACCTTTCCT16GENIChomozygous60916785
1160453819160453820CCA28GENIChomozygous60916786
1160455188160455189GT17GENICpossibly homozygous60916788
1160455280160455281TTA29GENICpossibly homozygous61771914
1160456288160456289TC22GENIChomozygous61771916
1160457564160457565GA34GENIChomozygous60916793
1160458679160458680CCAAAA16GENICpossibly homozygous60916795
1160458679160458680CCAAA16GENICheterozygous60916796
1160458697160458698GA22GENICheterozygous60916797
1160459631160459632CA14GENIChomozygous60916799
1160460334160460335AATATGTG13GENICheterozygous60916801
1160460372160460373GA18GENICheterozygous60916802
1160462657160462658CCAA1GENIChomozygous60916804
1160463594160463595CT18GENIChomozygous60916805
1160463799160463800TC17GENIChomozygous60916806
1160464101160464102AG13GENIChomozygous60916807
1160465611160465612CCAA7GENICpossibly homozygous60916809
1160465627160465628TG20GENICpossibly homozygous61547163
1160465680160465681TA26GENICpossibly homozygous61771918
1160465895160465896A-29GENIChomozygous60916810
1160466013160466023AAAAAAAAAA----------9GENIChomozygous61771920
1160467053160467054GGAAAA18GENIChomozygous61678499
1160467634160467638AGGA----31GENIChomozygous60916815
1160468223160468224TC21GENIChomozygous60916817
1160472290160472291GC24GENIChomozygous61771922