chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106361612763616128TG1GENIChomozygous590014527
106361647863616479GA9GENICpossibly homozygous590014528
106361653563616536TTA11GENIChomozygous723335623
106361660963616610CT19GENIChomozygous590014529
106361826163618262AG7GENIChomozygous591666101
106361853363618535CT--8GENIChomozygous723335624
106361863863618639AG8GENIChomozygous591666102
106361938263619383GA7GENICpossibly homozygous591666103
106361956363619564CG16GENICpossibly homozygous591666104
106361959363619594AG9GENIChomozygous591666105
106361997463619975GA11GENICpossibly homozygous591666106
106362040263620403TTG14GENICpossibly homozygous723335625
106362061063620611CG12GENIChomozygous591666107
106362082363620824AG14GENICheterozygous591666108
106362093863620939GGGAGA4GENICheterozygous723335626
106362176363621764TC14GENIChomozygous590014530
106362179263621793CT16GENICpossibly homozygous590014531
106362200863622009CT12GENICpossibly homozygous590014532
106362211763622118AC12GENIChomozygous590014533
106362213863622139AG14GENIChomozygous590014534
106362280363622804GA12GENIChomozygous590014535
106362422963624230A-8GENICheterozygous723335627
106362446063624461AG8GENICpossibly homozygous591666109
106362449963624500TC11GENIChomozygous591666110
106362496863624969GC22GENIChomozygous590014536
106362558863625589TC9GENICpossibly homozygous590014537
106362604763626048TG15GENICpossibly homozygous590014538
106362651263626513AG13GENIChomozygous591666111
106362681863626819AG4GENIChomozygous591666112
106362684563626846AATTT3GENICheterozygous723335628
106362785363627854CG8GENIChomozygous590014539
106362805163628052TC10GENIChomozygous590014540
106362857663628577TG2GENIChomozygous590014541
106363068163630682AC11GENIChomozygous590014542
106363195063631951GT6GENICheterozygous590014543
106363207063632071TG6GENICheterozygous590014544
106363236763632376TCATGGGCA---------1GENIChomozygous723335629
106363248063632481AAT1GENIChomozygous723335630
106363339763633398AAG7GENIChomozygous723335631