chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14103266002103266003CT24GENIChomozygous139612445
14103266646103266647GA16GENIChomozygous139612446
14103266918103266919AT5GENICheterozygous154878326
14103267745103267746AG18GENIChomozygous139612447
14103266918103266919A5GENICheterozygous403656464
14103267979103267980AG17GENIChomozygous140915390
14103268010103268011AG9GENIChomozygous140915391
14103269190103269191GA12GENIChomozygous139612448
14103269256103269257AG15GENIChomozygous139612449
14103270038103270039CG15GENIChomozygous139612450
14103270762103270763AC22GENIChomozygous139612451
14103271338103271339TG13GENIChomozygous139612452
14103272332103272333GC17GENIChomozygous139612453
14103273258103273259AG9GENIChomozygous139612454
14103273820103273821AC20GENIChomozygous139612455
14103273867103273868CT21GENIChomozygous139612456
14103274876103274877GA21GENIChomozygous139612457
14103274913103274914AC27GENIChomozygous139612458
14103276368103276369AC19GENIChomozygous139612459
14103273339103273340A14GENIChomozygous139414621
14103277171103277171ATT17GENIChomozygous139414623
14103269819103269828ATTCAGTGT13GENIChomozygous139414619
14103273013103273049TTCCCTCCCTCTCCCCTTCCTTCCCTCCCTCTTCCC3GENIChomozygous139414620
14103277170103277170TTTTAA17GENIChomozygous139414622
14103277173103277175GC17GENIChomozygous139414624
14103277177103277177TAATTTATA16GENIChomozygous139414625
14103277728103277729CT19GENIChomozygous139612460
14103278357103278358TC20GENIChomozygous139612461
14103282611103282611A8GENIChomozygous139414626
14103282834103282835AG14GENIChomozygous139612462
14103283947103283948CT26GENIChomozygous139612463
14103284190103284191CT25GENIChomozygous139612464
14103284252103284253CT25GENIChomozygous139612465
14103284477103284478AG17GENIChomozygous139612466
14103285725103285726A23GENIChomozygous139414627