chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------12GENIChomozygous689334780
85378107053781071CT18GENIChomozygous517064190
85378121053781211AG27GENIChomozygous517064191
85378128753781288GGAA14GENICheterozygous689334781
85378128753781288GGAAA14GENICheterozygous689334782
85378128753781288GGA14GENICheterozygous689334783
85378133353781334AG19GENIChomozygous517064192
85378146653781467AG24GENIChomozygous517064193
85378180553781806AG21GENIChomozygous517064194
85378193153781932TTTA7GENIChomozygous689334785
85378200853782013GTTTG-----8GENIChomozygous689334786
85378201253782013G-13GENICheterozygous689334787
85378241353782414CT23GENIChomozygous517064195
85378260753782608TC20GENIChomozygous517064196
85378277053782771GA19GENICpossibly homozygous517064197
85378331953783320AG33GENIChomozygous517064198
85378340253783403T-8GENIChomozygous689334788
85378373853783739GT17GENIChomozygous517064199
85378379353783794TC17GENIChomozygous517064200
85378391753783918T-19GENICheterozygous689334789
85378391953783926TGCGTGT-------23GENICpossibly homozygous689334790
85378393753783938TC33GENICheterozygous517064201
85378404853784049TC34GENIChomozygous517064202
85378438353784384A-19GENIChomozygous689334791
85378550553785506T-10GENICheterozygous689334792
85378550753785508TTTTTTTC11GENIChomozygous689334793
85378632153786323AC--1GENIChomozygous689334794