chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1109727493109727494TC15GENIChomozygous60789712
1109727761109727762TTTG9GENIChomozygous62554163
1109727818109727819TC17GENIChomozygous60789713
1109728936109728937A-14GENIChomozygous60789714
1109729045109729046TG12GENIChomozygous60789715
1109729455109729456TC27GENIChomozygous60789716
1109730320109730322AT--25GENIChomozygous60789717
1109730351109730352CCT26GENIChomozygous60789718
1109730562109730563AG23GENIChomozygous60789722
1109730648109730649GGA19GENIChomozygous60789723
1109731042109731043AG24GENIChomozygous60789724
1109731294109731295TA21GENIChomozygous61500185
1109727954109727955AAT12GENIChomozygous61500180
1109729642109729643TC28GENIChomozygous61500181
1109730421109730422TC19GENIChomozygous61500182
1109730870109730871GA20GENIChomozygous61500183
1109731019109731020TG24GENIChomozygous61500184
1109731470109731471AT17GENIChomozygous60789725
1109731512109731513TC18GENIChomozygous61500186
1109731617109731618TC27GENIChomozygous60789726
1109732013109732015TT--16GENIChomozygous61500187
1109732178109732179AG33GENIChomozygous60789728
1109732279109732280CG22GENIChomozygous60789729
1109732413109732414AAT7GENIChomozygous61500188
1109732762109732763CT18GENIChomozygous61500189
1109732950109732951GA24GENIChomozygous61500190
1109733036109733037GA22GENIChomozygous61500191
1109733117109733118AG23GENIChomozygous61500192
1109733474109733475C-20GENICpossibly homozygous61500193
1109733664109733666AC--23GENICheterozygous62150267
1109733671109733672AACATG23GENICheterozygous62150269
1109733677109733681GCGA----29GENICheterozygous62229989
1109733501109733502TTA17GENICheterozygous62085829
1109733504109733505TTA18GENICheterozygous62085830
1109733509109733510CCA18GENICheterozygous62085831