chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14103266002103266003CT9GENIChomozygous139612445
14103266646103266647GA8GENIChomozygous139612446
14103267745103267746AG12GENIChomozygous139612447
14103269190103269191GA13GENIChomozygous139612448
14103269256103269257AG15GENIChomozygous139612449
14103270038103270039CG10GENIChomozygous139612450
14103270762103270763AC12GENIChomozygous139612451
14103271338103271339TG16GENIChomozygous139612452
14103272332103272333GC15GENIChomozygous139612453
14103273258103273259AG4GENIChomozygous139612454
14103273820103273821AC16GENIChomozygous139612455
14103273867103273868CT14GENIChomozygous139612456
14103274876103274877GA16GENIChomozygous139612457
14103274913103274914AC17GENIChomozygous139612458
14103276368103276369AC8GENIChomozygous139612459
14103277173103277175GC12GENIChomozygous139414624
14103267979103267980AG11GENIChomozygous140915390
14103268010103268011AG9GENIChomozygous140915391
14103269819103269828ATTCAGTGT11GENIChomozygous139414619
14103273013103273049TTCCCTCCCTCTCCCCTTCCTTCCCTCCCTCTTCCC6GENIChomozygous139414620
14103273339103273340A11GENIChomozygous139414621
14103277170103277170TTTTAA12GENIChomozygous139414622
14103277171103277171ATT12GENIChomozygous139414623
14103277177103277177TAATTTATA12GENIChomozygous139414625
14103277728103277729CT14GENIChomozygous139612460
14103278357103278358TC17GENIChomozygous139612461
14103282611103282611A8GENIChomozygous139414626
14103282834103282835AG13GENIChomozygous139612462
14103283947103283948CT13GENIChomozygous139612463
14103284190103284191CT13GENIChomozygous139612464
14103284477103284478AG13GENIChomozygous139612466
14103285725103285726A19GENIChomozygous139414627