chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
33843193338431934TG64GENICpossibly homozygous111545961
33843394138433942TG57GENIChomozygous111903266
33843397738433978AC61GENICpossibly homozygous111903268
33843414038434141TG65GENIChomozygous111545962
33843414138434142GT62GENIChomozygous111903270
33843431738434318CG34GENIChomozygous111545963
33844069338440694CT6GENIChomozygous111903272
33844899838448999GC32GENICheterozygous111903274
33845084338450844AT71GENIChomozygous111545965
33849906838499069AC15GENICpossibly homozygous111903276
33850329038503291CT31GENIChomozygous111545966
33850351638503517TC56GENIChomozygous111545967
33850356338503564CA47GENIChomozygous111545968
33850367838503679TC49GENIChomozygous111545969
33850574838505749GT37GENIChomozygous111545970
33850585438505855TC81GENIChomozygous111545971
33850601438506015AC38GENIChomozygous111545972
33851158338511584AG42GENIChomozygous111545973
33852323438523235GT23GENICpossibly homozygous111545974
33852427638524277CT23GENIChomozygous111545975
33853146738531468GC62GENICheterozygous111545976
33856994038569941TC13GENICpossibly homozygous111545977
33856994438569945CT16GENICpossibly homozygous111545978
33858388838583889CA46GENICpossibly homozygous111903278
33859468638594687TC12GENICheterozygous111903280
33865979738659798AC18GENICpossibly homozygous111545980