chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103929802739298028CA24GENIChomozygous967518424
103930810739308108AG25GENIChomozygous967518425
103930858339308584AC19GENIChomozygous967518426
103931007039310071TC24GENIChomozygous967518427
103931030739310308CT29GENIChomozygous967518428
103931064539310646CT53GENIChomozygous967518429
103931528839315289AG37GENIChomozygous967518430
103931628839316289TC31GENIChomozygous967518431
103931691439316915CT24GENIChomozygous967518432
103931697239316973TG22GENIChomozygous967518433
103931697739316978CT24GENIChomozygous967518434
103931718139317182AC40GENIChomozygous967518435
103931744539317446GC32GENIChomozygous967518436
103931745639317457GA28GENIChomozygous967518437
103931766839317669AC31GENIChomozygous967518438
103931803639318037CT23GENIChomozygous967518439
103931893939318940GA22GENIChomozygous967518440
103931951939319520TC32GENIChomozygous967518441
103932015639320157CG20GENIChomozygous967518442
103932067939320680GA27GENIChomozygous967518443
103932095839320959CA41GENIChomozygous967518444
103932098639320987GA45GENIChomozygous967518445
103932099939321000GA46GENIChomozygous967518446
103932129639321297AG35GENIChomozygous967518447
103932134339321344TC31GENIChomozygous967518448
103932137539321376CA31GENIChomozygous967518449
103932139539321396CT32GENIChomozygous967518450
103932142339321424TC27GENIChomozygous967518451
103932144539321446TG24GENIChomozygous967518452
103932168039321681AC22GENIChomozygous967518453
103932199239321993TC21GENIChomozygous967518454
103932211239322113AG26GENIChomozygous967518455
103932251339322514GC44GENIChomozygous967518456
103932319339323194GA34GENIChomozygous967518457
103932387439323875TC19GENIChomozygous967518458
103932389339323894AT17GENIChomozygous967518459
103932403839324039GA18GENIChomozygous967518460
103932416239324163TA14GENIChomozygous967518461
103932431539324316CT37GENIChomozygous967518462