chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1160452587160452588TTGCTCTTGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAG6GENIChomozygous62090325
1160452672160452673TC17GENIChomozygous60916783
1160452911160452912TA35GENIChomozygous60916784
1160453401160453402AATCTTCCTTTGAACCTTTCCT21GENIChomozygous60916785
1160453819160453820CCA28GENIChomozygous60916786
1160454539160454540TA14GENIChomozygous60916787
1160455779160455780GA8GENIChomozygous60916791
1160456213160456214GT25GENIChomozygous60916792
1160457564160457565GA16GENIChomozygous60916793
1160458273160458274TC20GENIChomozygous60916794
1160459121160459122CCA8GENIChomozygous60916798
1160458679160458680CCAAA2GENIChomozygous60916796
1160459631160459632CA17GENIChomozygous60916799
1160460372160460373GA3GENIChomozygous60916802
1160460848160460849GC7GENIChomozygous60916803
1160462412160462418CACACA------5GENICheterozygous62168980
1160462414160462418CACA----5GENICheterozygous62168982
1160462657160462658CCAA3GENIChomozygous60916804
1160463594160463595CT15GENIChomozygous60916805
1160463799160463800TC8GENIChomozygous60916806
1160464101160464102AG20GENIChomozygous60916807
1160464581160464582TTA12GENIChomozygous60916808
1160465611160465612CCAA11GENIChomozygous60916809
1160465895160465896A-11GENIChomozygous60916810
1160466017160466023AAAAAA------7GENICpossibly homozygous60916811
1160466064160466065CA15GENIChomozygous60916812
1160467053160467054GGA25GENIChomozygous60916813
1160467556160467557CG21GENIChomozygous60916814
1160467634160467638AGGA----18GENIChomozygous60916815
1160468189160468190GA30GENIChomozygous60916816
1160468223160468224TC28GENIChomozygous60916817
1160469346160469347CCAGAGAGTGATAG30GENIChomozygous62090327
1160469692160469693GA29GENIChomozygous60916819