chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005437210054373AC23INTERGENIChomozygous795618353
141005799910058000TC40INTERGENIChomozygous795618354
141005815810058159TA21INTERGENICheterozygous795618355
141005837210058373AG30INTERGENICpossibly homozygous795618356
141005839310058394AC31INTERGENICpossibly homozygous795618357
141005854510058546CA39INTERGENIChomozygous795618358
141005889610058897GA41INTERGENIChomozygous795618359
141006077010060771CT45GENIChomozygous795618360
141006082010060821AG45GENIChomozygous795618361
141006096610060967CT52GENICpossibly homozygous795618362
141006108710061088GC48GENIChomozygous795618363
141006114010061141CT42GENIChomozygous795618364
141006114210061143AT40GENIChomozygous795618365
141006115310061154TC42GENIChomozygous795618366
141006119810061199GA44GENIChomozygous795618367
141006129410061295GT22GENIChomozygous795618368
141006130210061303GT28GENICheterozygous795618369
141006131410061315AG28GENICheterozygous795618370
141006141410061415AC33GENIChomozygous795618371
141006142010061421GA35GENIChomozygous795618372
141006142310061424TA36GENIChomozygous795618373
141006144610061447CA30GENIChomozygous795618374
141006157910061580AG38GENIChomozygous795618375
141006158510061586AG38GENIChomozygous795618376
141006159510061596GA39GENIChomozygous795618377
141006163110061632CT40GENIChomozygous795618378
141006168610061687TC50GENIChomozygous795618379
141006169310061694AG44GENIChomozygous795618380
141006169410061695AG45GENIChomozygous795618381
141006170010061701CT49GENIChomozygous795618382
141006187310061874GA28GENIChomozygous795618383
141006187510061876CA30GENIChomozygous795618384