chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12408950524089506AG35GENIChomozygous592716324
12408956824089569TC27GENIChomozygous592716325
12409122124091222GC34GENIChomozygous594903145
12409244224092443GA43GENIChomozygous594903146
12409596824095969CA30GENIChomozygous594903147
12409648724096488GC23GENIChomozygous594903148
12409666424096665TG28GENIChomozygous594903149
12409680024096801AG27GENIChomozygous594903150
12409697924096980AG36GENIChomozygous592716326
12409728724097288AC27GENIChomozygous592716327
12409775424097755C-20GENIChomozygous724206662
12409798424097985CT26GENIChomozygous594903151
12409800824098009AC27GENIChomozygous592716328
12409842024098421TC38GENIChomozygous594903152
12409864224098643GC28GENIChomozygous592716329
12409896324098964CG25GENIChomozygous592716330
12409896424098965AG27GENIChomozygous594903153
12409897424098975AT29GENIChomozygous594903154
12409897524098976AG29GENIChomozygous594903155
12409898024098983GAC---30GENIChomozygous724206663
12409898424098985AATTT29GENIChomozygous724206664
12409898524098986GT29GENIChomozygous594903156
12409959024099591TTA10GENICpossibly homozygous724206665