chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181553329115533292CT16GENIChomozygous110452695
181553448315534484CT29GENIChomozygous110452696
181553452115534522TC22GENICpossibly homozygous110282346
181553457815534579TC13GENIChomozygous110282348
181553482015534821TA27GENIChomozygous110452697
181553519315535194CT20GENIChomozygous110282351
181553544815535449AG16GENIChomozygous110452698
181553569315535694TC14GENIChomozygous110282355
181553651615536517TC10GENIChomozygous110452699
181553654715536548GA13GENIChomozygous110452700
181553677615536777TC13GENIChomozygous110452701
181553682415536825CT16GENIChomozygous110452702
181553702715537028CT18GENIChomozygous110452703
181553732015537321TG19GENIChomozygous110282359
181553800215538003AG18GENIChomozygous110452707
181553421515534216A19GENICpossibly homozygous129518000
181553558815535588G10GENIChomozygous129518001
181553663815536639AG13GENIChomozygous110525657
181553740115537402TC18GENIChomozygous110452704
181553794215537943AG21GENIChomozygous110452705
181553799115537992TC17GENIChomozygous110452706
181553820815538209TC16GENIChomozygous110282361
181553875115538752AG19GENIChomozygous110452708
181553888315538884GA17GENIChomozygous110452709
181553924715539248CT15GENIChomozygous110452710
181553936715539368TC24GENIChomozygous110452711
181553939315539394AG27GENIChomozygous110452712
181553988615539887AC17GENIChomozygous110452714
181554058115540581T18GENIChomozygous129518003
181554071015540711TC17GENIChomozygous110282367
181554132015541321AG24GENIChomozygous110282369
181554202915542030GA21GENIChomozygous110282375
181553834915538359TGCTAGACAG16GENIChomozygous132226510
181553859115538591GACAGAAGAG17GENIChomozygous132226511