chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181553329115533292CT21GENIChomozygous110452695
181553358515533586CT23GENICheterozygous119516838
181553448315534484CT18GENIChomozygous110452696
181553452115534522TC22GENIChomozygous110282346
181553457815534579TC23GENIChomozygous110282348
181553482015534821TA27GENIChomozygous110452697
181553519315535194CT29GENIChomozygous110282351
181553544815535449AG31GENIChomozygous110452698
181553569315535694TC20GENIChomozygous110282355
181553651615536517TC17GENIChomozygous110452699
181553654715536548GA16GENIChomozygous110452700
181553663815536639AG7GENIChomozygous110525657
181553677615536777TC23GENIChomozygous110452701
181553682415536825CT19GENIChomozygous110452702
181553702715537028CT18GENIChomozygous110452703
181553732015537321TG14GENIChomozygous110282359
181553740115537402TC23GENIChomozygous110452704
181553794215537943AG25GENIChomozygous110452705
181553799115537992TC33GENIChomozygous110452706
181553800215538003AG32GENIChomozygous110452707
181553820815538209TC12GENIChomozygous110282361
181553875115538752AG22GENIChomozygous110452708
181553888315538884GA37GENIChomozygous110452709
181553924715539248CT30GENIChomozygous110452710
181553936715539368TC23GENIChomozygous110452711
181553939315539394AG21GENIChomozygous110452712
181553960615539607TC28GENICheterozygous110452713
181553988615539887AC27GENIChomozygous110452714
181554071015540711TC25GENIChomozygous110282367
181554132015541321AG17GENIChomozygous110282369
181554202915542030GA23GENIChomozygous110282375