chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------6GENIChomozygous697523624
85378107053781071CT33GENIChomozygous539136548
85378121053781211AG27GENIChomozygous539136549
85378128753781288GGAA4GENICheterozygous697523625
85378133353781334AG17GENIChomozygous539136550
85378146653781467AG27GENIChomozygous539136551
85378180553781806AG29GENIChomozygous539136552
85378193153781932TTTA5GENIChomozygous697523629
85378200853782013GTTTG-----17GENIChomozygous697523630
85378201253782013G-19GENICheterozygous697523631
85378241353782414CT35GENIChomozygous539136553
85378260753782608TC25GENIChomozygous539136554
85378277053782771GA28GENICpossibly homozygous539136555
85378331953783320AG35GENIChomozygous539136556
85378340253783403T-20GENIChomozygous697523632
85378373853783739GT20GENIChomozygous539136557
85378379353783794TC34GENIChomozygous539136558
85378391753783918T-19GENICheterozygous697523633
85378391953783926TGCGTGT-------19GENICpossibly homozygous697523634
85378404853784049TC27GENIChomozygous539136559
85378438353784384A-22GENIChomozygous697523635
85378550553785506T-2GENICheterozygous697523636
85378550753785508TTTTTTTC4GENICheterozygous697523637