chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8132713265132713266CT31GENIChomozygous117129877
8132714164132714165AG50GENIChomozygous117129879
8132714530132714531CT35GENIChomozygous117129881
8132714554132714555AG27GENIChomozygous117129883
8132714808132714809TC47GENIChomozygous117129885
8132714867132714868CT38GENIChomozygous117129887
8132714962132714963GA37GENIChomozygous117129889
8132715624132715625AG30GENIChomozygous117129891
8132715849132715850GA22GENIChomozygous117129893
8132715859132715860CG23GENIChomozygous116905340
8132716975132716976GA34GENIChomozygous117129897
8132717116132717117AT36GENIChomozygous117129899
8132717181132717182CT27GENIChomozygous117129901
8132717301132717302TG25GENIChomozygous117129903
8132717921132717922TA35GENIChomozygous116729805
8132721389132721390CT32GENIChomozygous116729809
8132721845132721846AG27GENIChomozygous116729810
8132724252132724253CT30GENIChomozygous116729813
8132725594132725595CT50GENIChomozygous117129911
8132726060132726061CT18GENIChomozygous117129913
8132726144132726145AT13GENIChomozygous116729815
8132726175132726176AT9GENIChomozygous117129915
8132727633132727634TA19GENIChomozygous117129917
8132728041132728042AG32GENIChomozygous117129919
8132729584132729585CT38GENIChomozygous118113376
8132733360132733361AG33GENIChomozygous116905352
8132735791132735792GA39GENIChomozygous116905356
8132735861132735862AG76GENIChomozygous116729821
8132738051132738052CT17GENIChomozygous116729823
8132738084132738085AG14GENIChomozygous116905364
8132738518132738519TC20GENIChomozygous116905366
8132741341132741342TG19GENIChomozygous116905368
8132741985132741986GA11GENIChomozygous116905370
8132742289132742290TC28GENIChomozygous116905372
8132748845132748846GA7GENIChomozygous116905388
8132749200132749201CT27GENIChomozygous116905390
8132749216132749217CT26GENIChomozygous116905392
8132750284132750285GA20GENIChomozygous116905394
8132750798132750799GA25GENIChomozygous116905396
8132751349132751350AG50GENIChomozygous116729837
8132752803132752804AG60GENIChomozygous116905398