chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104856968848569689CCA13GENIChomozygous53332885
104857031448570315CCTTTCT30GENIChomozygous51640108
104857074348570744GGAA17GENIChomozygous53332888
104857142348571424GT23GENIChomozygous51640110
104857233548572336AG23GENIChomozygous51640111
104857303548573036GT18GENIChomozygous51640112
104857338248573383AG20GENIChomozygous53332891
104857352348573524TA29GENIChomozygous51640113
104857518148575183TT--11GENIChomozygous53332894
104857153448571535CCA16GENIChomozygous51447068
104857434748574348CT10GENIChomozygous51447070
104857436748574368GA5GENIChomozygous51447071
104857441648574417CA12GENIChomozygous52318317
104857531048575311T-14GENIChomozygous51640115
104857823448578235TC29GENIChomozygous51640119
104857873048578734ACAC----10GENICheterozygous51640120
104858079448580910AGGGCATTTTCTTGGCTTTTTTTTTTTTTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC--------------------------------------------------------------------------------------------------------------------23GENICpossibly homozygous52459790
104857729548577301GTGTGT------6GENIChomozygous52374360
104857873248578734AC--10GENICheterozygous51877449
104858284148582842GT35GENIChomozygous51640125
104858285548582856GA37GENIChomozygous51640126
104858288348582884GA33GENIChomozygous51640127
104858294748582948CT17GENIChomozygous51640128
104858296948582970AAC19GENIChomozygous51447078
104858392448583936CTCTCTCCCCCC------------3GENICheterozygous52374364
104858436348584364T-11GENIChomozygous52055633
104858468548584695GTGTGTGTGT----------7GENICheterozygous51447080
104858468748584695GTGTGTGT--------7GENICheterozygous51877453
104858503448585035AG26GENIChomozygous52055635
104858522148585222TTTGTG6GENICheterozygous52374368
104858522148585222TTTGTGTG6GENICheterozygous52374370
104858532248585323TA20GENIChomozygous52055637