chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64319286043192862GT--5GENICheterozygous55496435
64319294943192950T-5GENICheterozygous54363235
64321087143210877GTGTGT------4GENICheterozygous55496439
64322587543225879TACA----10GENICheterozygous55496445
64324380543243806GGCGCACGTGC10GENIChomozygous55496449
64324381443243815TG15GENIChomozygous55496451
64324382543243826CG19GENIChomozygous54363243
64324392543243926A-11GENIChomozygous54363245
64324394043243941TTGGGAAAG7GENIChomozygous55496453
64324394443243945TC6GENIChomozygous54363255
64324394943243950GA6GENIChomozygous54363257
64324395443243957TTT---6GENIChomozygous55496455
64324395743243958TTCA6GENIChomozygous55496457
64324396043243961GGCCA8GENIChomozygous55496459
64324396243243963TG9GENIChomozygous55496461
64324397443243975TC10GENIChomozygous55496463
64324397843243979AC11GENIChomozygous55496465
64324398043243981AC12GENIChomozygous55496467
64324398443243985AC14GENIChomozygous55496469
64324399143243992AT13GENIChomozygous55496471
64324399343243994AT13GENIChomozygous55496473
64324399543243996TC13GENIChomozygous55496475
64324401143244012TTTA17GENIChomozygous54363259
64324401343244014AT20GENIChomozygous55496477
64324401643244018AC--20GENIChomozygous54363261
64321086943210877GTGTGTGT--------4GENICheterozygous55602901
64324391543243916CA12GENIChomozygous55405514
64324391843243919AT12GENIChomozygous55405517
64324391943243920CT12GENIChomozygous55405519