chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71126851611268517TC38GENIChomozygous115568122
71126913911269140GA20GENICpossibly homozygous115568123
71126962711269628GA20GENIChomozygous115568124
71127022611270227GA20GENIChomozygous115568125
71127270911272710AG19GENIChomozygous115568130
71127277011272771TC27GENIChomozygous115568132
71127298311272984GA19GENIChomozygous115568133
71127401511274016CG23GENIChomozygous115568134
71127406211274063TC26GENIChomozygous115568135
71127486011274861GA47GENIChomozygous115568136
71127567711275678TC31GENIChomozygous115568137
71127576511275766TC19GENIChomozygous115568138
71127634611276347TC20GENIChomozygous115568139
71127649611276497TC29GENIChomozygous115568140
71127660311276604TC16GENIChomozygous115568141
71127724011277241AG30GENIChomozygous115568142
71127727811277279GT30GENIChomozygous116273677
71127729711277298GA30GENIChomozygous115568143
71127813111278132GA38GENIChomozygous115568145
71127835011278351TC33GENIChomozygous115568147
71127869211278693AG44GENIChomozygous115568149
71127909711279098GA33GENIChomozygous115568150
71127964611279647CT41GENIChomozygous115568151
71128008911280090AG22GENIChomozygous115568152
71128009411280095AG20GENIChomozygous115568153
71128009511280096AG20GENIChomozygous115568154
71128036311280364GA33GENIChomozygous115568155
71128053111280532AG32GENIChomozygous115568156
71128309311283094CT43GENIChomozygous115568158
71128512811285129TC31GENIChomozygous115568159
71128516811285169GA32GENIChomozygous115568160
71128938911289390GA42GENIChomozygous116273679
71128968711289688AC19GENIChomozygous115568174
71128969511289696TG20GENIChomozygous115568175
71129110911291110GA36GENIChomozygous115568180
71129149511291496TG31GENIChomozygous115568181