chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71120191311201914TC18GENIChomozygous53787681
71120353211203533GA21GENICpossibly homozygous53787682
71120427211204273GA20GENIChomozygous53787684
71120459011204591GA16GENIChomozygous53787686
71120468811204692CCCC----5GENICheterozygous53787687
71120706611207067AACCTACCCACCCACTCACCCATCCACCACCCATCTATCCACCCACTCATCTAACCACCCACTCACCCATCTAACCACCCACCCATCCACCCATCTATCTACCCTCCCACCTACCCACCCACC10GENIChomozygous54954313
71120893511208938CCC---12GENIChomozygous54954315
71120893911208988CACTGCGGGGATTCTGGGCGGGGCTCCACTCCTGACCACGCCCCTTAAC-------------------------------------------------18GENIChomozygous54884817
71120907811209081ACG---21GENIChomozygous53787697
71120916711209168AG21GENIChomozygous53787698
71121076111210764TGT---8GENIChomozygous53787701
71121076511210774TGTATGTAC---------7GENIChomozygous53787703
71121088411210885CT13GENIChomozygous53787704
71121203011212031CT23GENIChomozygous53787706
71121216011212161AG19GENIChomozygous53787707
71121250411212505AG17GENIChomozygous53787709
71121260511212606GA17GENIChomozygous53787711
71121303711213038GC20GENIChomozygous53787712
71121341111213412TC25GENIChomozygous53787714
71121377411213775GA20GENIChomozygous53787716