chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181553346215533463CT28GENIChomozygous110282344
181553421515534216A59GENIChomozygous129518000
181553452115534522TC49GENIChomozygous110282346
181553457815534579TC46GENIChomozygous110282348
181553519315535194CT36GENIChomozygous110282351
181553540215535403TG40GENICpossibly homozygous110282353
181553558815535588G38GENIChomozygous129518001
181553569315535694TC57GENIChomozygous110282355
181553604115536042GA43GENIChomozygous110282357
181553732015537321TG66GENIChomozygous110282359
181553820815538209TC62GENIChomozygous110282361
181553959015539590TC35GENICpossibly homozygous129518002
181554016815540169CT51GENIChomozygous110282363
181554058115540581T56GENIChomozygous129518003
181554057015540571TA55GENIChomozygous110282365
181554071015540711TC55GENIChomozygous110282367
181554132015541321AG73GENIChomozygous110282369
181554132815541329CT73GENIChomozygous110282371
181554184015541841CT71GENIChomozygous110282373
181554202915542030GA70GENIChomozygous110282375