chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1271502464271502465CA12GENIChomozygous61332247
1271503100271503101TA12GENIChomozygous61332248
1271504386271504387TC13GENIChomozygous61218961
1271504595271504596AAT23GENIChomozygous61218963
1271504911271504912GA12GENIChomozygous61218965
1271505217271505218TC13GENIChomozygous61218969
1271505280271505281CCAGTT11GENIChomozygous61218971
1271505301271505302CT11GENIChomozygous61218973
1271505421271505422AG18GENIChomozygous61218975
1271505778271505779GT25GENIChomozygous61218977
1271506826271506827AAAAAAC14GENIChomozygous61218981
1271506923271506924AG19GENIChomozygous61218983
1271507154271507155TG7GENIChomozygous61218985
1271507543271507544GA24GENIChomozygous61332249
1271507561271507562CT25GENIChomozygous61218987
1271507908271507909AG17GENIChomozygous61218989
1271508011271508012TC13GENIChomozygous61218991
1271509427271509431AGAC----16GENIChomozygous61332250
1271509618271509619TC9GENIChomozygous61219001
1271509980271509981TC18GENIChomozygous61219003
1271510213271510214AG13GENIChomozygous61219005
1271510407271510408CCTT4GENIChomozygous61332251
1271510426271510427T-6GENICheterozygous61219011
1271504987271504988CA1GENIChomozygous62242305
1271504990271504991CA1GENIChomozygous62242306
1271510793271510794AACACACACACACACGCG8GENICheterozygous62242307
1271510795271510796AACACACACACACGCG10GENICheterozygous62242308
1271510983271510984TC14GENIChomozygous61219015
1271511381271511382TG13GENIChomozygous61332253
1271511492271511493GA11GENIChomozygous61219017
1271512811271512812GA22GENIChomozygous61332254
1271513710271513711CT23GENIChomozygous61332255
1271514129271514130CT25GENIChomozygous61332256
1271514306271514307GA18GENIChomozygous61219021
1271514730271514731T-14GENIChomozygous61332257