chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124759090247590903CT58GENIChomozygous115344446
124759099247590993AG54GENIChomozygous115344448
124759165647591657AT34GENIChomozygous115344450
124759619447596195GA44GENIChomozygous115344452
124759699747596998GC19GENIChomozygous115344454
124759947847599479TA46GENIChomozygous115344456
124760046347600464AG51GENIChomozygous115344458
124760129647601297AT47GENIChomozygous115344460
124760210147602102GA52GENIChomozygous115344462
124760298047602981TC37GENIChomozygous115344464
124760529947605300AG43GENIChomozygous115344466
124760559047605591GA35GENIChomozygous115344468
124760632447606325TC32GENIChomozygous115344470
124760792847607929TC53GENIChomozygous115344472
124760901947609020AG38GENIChomozygous115344475
124760951247609513AG46GENIChomozygous115344477
124760974147609742GA53GENIChomozygous115344479
124760981547609816CT51GENIChomozygous115344481
124761005947610060CT43GENIChomozygous115344483
124761023747610238CT34GENIChomozygous115344485
124761025847610259CT33GENIChomozygous115344487
124761138047611381AG30GENIChomozygous115344489
124761225547612256AC53GENIChomozygous115344491
124761312147613122AG53GENIChomozygous115344493
124761440947614410AT42GENIChomozygous115344496
124761478047614781CA56GENIChomozygous115344498
124761540747615408GT34GENICpossibly homozygous115344500
124761838847618389GC52GENIChomozygous115344502
124761925347619254AG24GENIChomozygous115344504
124762053647620537AG56GENIChomozygous115344506
124762133847621339AG38GENIChomozygous115344508
124762306747623068GA53GENIChomozygous115344510
124762325247623253CT36GENIChomozygous115344512
124762674747626748CT28GENIChomozygous115344514
124762751647627517TA40GENIChomozygous115344516
124762763347627634TC46GENIChomozygous115344518
124762790247627903CG51GENIChomozygous115344520
124762840347628404AG19GENIChomozygous115344522