chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181553329115533292CT36GENIChomozygous110452695
181553358515533586CT13GENICheterozygous119516838
181553448315534484CT40GENIChomozygous110452696
181553452115534522TC33GENIChomozygous110282346
181553457815534579TC34GENICpossibly homozygous110282348
181553482015534821TA30GENIChomozygous110452697
181553519315535194CT42GENIChomozygous110282351
181553544815535449AG39GENIChomozygous110452698
181553569315535694TC32GENIChomozygous110282355
181553651615536517TC46GENIChomozygous110452699
181553654715536548GA58GENIChomozygous110452700
181553663815536639AG58GENIChomozygous110525657
181553671215536713CT42GENICheterozygous119516840
181553677615536777TC24GENIChomozygous110452701
181553682415536825CT27GENIChomozygous110452702
181553702715537028CT47GENIChomozygous110452703
181553732015537321TG41GENIChomozygous110282359
181553740115537402TC38GENICpossibly homozygous110452704
181553794215537943AG30GENIChomozygous110452705
181553799115537992TC21GENIChomozygous110452706
181553800215538003AG24GENIChomozygous110452707
181553820815538209TC35GENIChomozygous110282361
181553875115538752AG42GENIChomozygous110452708
181553888315538884GA30GENIChomozygous110452709
181553924715539248CT38GENIChomozygous110452710
181553936715539368TC39GENIChomozygous110452711
181553939315539394AG40GENIChomozygous110452712
181553960615539607TC70GENICheterozygous110452713
181553965315539654CT68GENICheterozygous119482686
181553988615539887AC32GENIChomozygous110452714
181554071015540711TC42GENIChomozygous110282367
181554132015541321AG33GENIChomozygous110282369
181554202915542030GA43GENIChomozygous110282375