chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186834516968345170AC16GENICheterozygous404421013
186834532068345321TC50GENIChomozygous142670457
186834783668347837GA53GENIChomozygous142670458
186834975768349758GT47GENIChomozygous142670459
186835153768351538AG36GENIChomozygous142670460
186835153968351540AG35GENIChomozygous142670461
186835154068351541CT35GENIChomozygous142670462
186835295668352957CT44GENIChomozygous142670463
186835337068353371TC24GENIChomozygous155057781
186835153668351536GG36GENIChomozygous142634406
186835225068352250ACACCTACTCCTACAAGGCC33GENIChomozygous142634407
186835281568352816G51GENIChomozygous142634408
186835337068353371TG24GENICheterozygous403438707
186835339768353398TC22GENIChomozygous142670464
186835341168353412AG24GENIChomozygous142670465
186835348568353486CT40GENIChomozygous142670466
186835349068353491CT40GENIChomozygous142670467
186835350868353509TC41GENIChomozygous142670468
186835351268353513AT42GENIChomozygous142670469
186835354068353541TC47GENIChomozygous142670470
186835417068354171AC64GENIChomozygous142670471
186835631268356313TC49GENIChomozygous142670472
186835683468356834C59GENIChomozygous142634409
186836633568366336CT45GENIChomozygous142670475
186836923568369239AAAT41GENIChomozygous142634411
186837009568370096GA35GENIChomozygous142670476
186837028868370288TATGTATGTATG24GENIChomozygous142634412
186837031868370319CT24GENIChomozygous142670477
186837033868370339CT22GENIChomozygous155057791
186837033868370339C22GENICheterozygous404099663
186837068768370688GA35GENIChomozygous142670478