chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1138550521138550522TG28GENIChomozygous135679483
1138551048138551049TC21GENIChomozygous135679484
1138552584138552585TG15GENIChomozygous135679485
1138554187138554188AG22GENIChomozygous135679486
1138557103138557104CA20GENIChomozygous135679487
1138558090138558091AG16GENIChomozygous135679488
1138561079138561080AG26GENIChomozygous135679489
1138561562138561563AG31GENIChomozygous135679490
1138561605138561606TC25GENIChomozygous135679491
1138561709138561710TG13GENIChomozygous135679492
1138562543138562544GA18GENIChomozygous135679493
1138562636138562637TC15GENIChomozygous135679494
1138562658138562659CT18GENIChomozygous135679495
1138562704138562705AG18GENIChomozygous135679496
1138563240138563249TGAGGAAGG6GENIChomozygous140850537
1138563945138563946AC29GENIChomozygous135679497
1138564778138564779GA20GENIChomozygous135679498
1138566498138566499GA29GENIChomozygous135679499
1138566558138566559TC27GENIChomozygous135679500
1138566586138566587TC30GENIChomozygous135679501
1138566813138566814TC36GENIChomozygous135679502
1138567129138567130GA23GENIChomozygous135679503
1138567735138567736TC21GENIChomozygous135679504
1138568297138568298GA23GENIChomozygous135679505
1138569141138569142CT28GENIChomozygous135679506
1138569244138569245AG16GENIChomozygous135679507
1138569797138569798TC22GENIChomozygous135679508
1138570949138570950GA19GENIChomozygous135679509
1138571521138571522CT24GENIChomozygous135679510
1138563647138563649AA12GENIChomozygous135431943
1138564580138564586AGTAAT23GENIChomozygous135431944
1138565197138565197A17GENIChomozygous135431945
1138568340138568344AATG24GENIChomozygous135431946
1138570860138570863TGA19GENIChomozygous135431947