chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1160452587160452588TTGCTCTTGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAG7GENIChomozygous62090325
1160452672160452673TC22GENIChomozygous60916783
1160452911160452912TA23GENIChomozygous60916784
1160453401160453402AATCTTCCTTTGAACCTTTCCT34GENIChomozygous60916785
1160453819160453820CCA25GENIChomozygous60916786
1160454539160454540TA22GENIChomozygous60916787
1160455779160455780GA24GENIChomozygous60916791
1160456213160456214GT25GENIChomozygous60916792
1160457564160457565GA37GENIChomozygous60916793
1160458273160458274TC19GENIChomozygous60916794
1160458679160458680CCAAA4GENICheterozygous60916796
1160458679160458680CCAAAAA4GENICheterozygous62168976
1160459121160459122CCA19GENIChomozygous60916798
1160459631160459632CA16GENIChomozygous60916799
1160460334160460335AATATGTG16GENICpossibly homozygous60916801
1160460334160460335AATGTG16GENICheterozygous62168978
1160460372160460373GA14GENIChomozygous60916802
1160460848160460849GC18GENIChomozygous60916803
1160462412160462418CACACA------13GENICheterozygous62168980
1160462414160462418CACA----13GENICheterozygous62168982
1160462657160462658CCAA9GENICheterozygous60916804
1160463594160463595CT19GENIChomozygous60916805
1160463799160463800TC13GENIChomozygous60916806
1160464101160464102AG25GENIChomozygous60916807
1160464581160464582TTA17GENIChomozygous60916808
1160465611160465612CCAA12GENIChomozygous60916809
1160465895160465896A-11GENIChomozygous60916810
1160466017160466023AAAAAA------4GENIChomozygous60916811
1160466064160466065CA15GENIChomozygous60916812
1160467053160467054GGA28GENIChomozygous60916813
1160467556160467557CG18GENIChomozygous60916814
1160467634160467638AGGA----26GENIChomozygous60916815
1160468189160468190GA22GENIChomozygous60916816
1160468223160468224TC25GENIChomozygous60916817
1160469346160469347CCAGAGAGTGATAG23GENIChomozygous62090327
1160469692160469693GA27GENICpossibly homozygous60916819