chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48768820687688207GT26GENIChomozygous113281422
48768825787688258AT31GENIChomozygous112769505
48768826287688263GT30GENIChomozygous112769506
48768851687688517CG9GENIChomozygous112769509
48768900887689009CT24GENIChomozygous113281423
48768907587689076TA39GENIChomozygous113281424
48768918187689182AT20GENIChomozygous112769512
48769144887691449AG19GENIChomozygous112769520
48769254387692544TC41GENIChomozygous112769525
48769296587692966AG26GENIChomozygous112769528
48769347087693471TC25GENIChomozygous113281426
48769355787693558TA29GENIChomozygous113281427
48769443287694433GT38GENIChomozygous119341474
48769443387694434TG37GENIChomozygous119341476
48769567687695677AC36GENIChomozygous112769539
48769571587695716TC45GENIChomozygous113281429
48769699687696997CT30GENIChomozygous113281435
48769710487697105AG33GENIChomozygous113281436
48769734987697350AG17GENIChomozygous112769546
48769737887697379TC21GENIChomozygous112769547
48769803287698033GA37GENIChomozygous112769550
48769839287698393GT45GENIChomozygous112769552
48769851287698513AG36GENIChomozygous113281437
48769889687698897TC30GENIChomozygous113281438
48769890287698903TC29GENIChomozygous112769553
48769911587699116TC28GENIChomozygous113281439
48769965387699654GA26GENIChomozygous112769554
48769988887699889GA36GENIChomozygous112769555
48770125487701255CA34GENIChomozygous112769561
48770159787701598GT23GENIChomozygous113281440
48770253987702540GA26GENIChomozygous113281441
48770270387702704GA27GENIChomozygous113281442
48770286187702862TG23GENIChomozygous112769566
48770297987702980GC21GENIChomozygous113281443
48770324987703250TG16GENIChomozygous112769569
48770331687703317GA28GENIChomozygous112769571
48770366787703668TA23GENIChomozygous113281444
48770382487703825AC21GENIChomozygous112769575
48770457987704580AG22GENIChomozygous112769579
48770467987704680CG26GENIChomozygous113281445