chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173290336632903367GA83GENICheterozygous119280594
173290341132903412CT110GENICheterozygous119280596
173290342932903430TC111GENICheterozygous119280598
173290345432903455GA118GENICheterozygous119280600
173290360532903606CT103GENICheterozygous119280602
173290361032903611AT105GENICheterozygous119280604
173290372932903730AG113GENICheterozygous119280606
173290384032903841CT105GENICheterozygous111192328
173290386132903862AG105GENICheterozygous119280608
173290396532903966AG94GENICheterozygous119280610
173290405532904056CG94GENICheterozygous119280612
173290405732904058GA94GENICheterozygous119280614
173290406532904066CT105GENICheterozygous119280616
173290412632904127AC119GENICheterozygous119280618
173290419132904192AG109GENICheterozygous119280620
173290427432904275CG112GENICheterozygous119280622
173290435632904357CT68GENICheterozygous111499528
173290504832905049CG39GENIChomozygous111031164
173290525432905255TC49GENIChomozygous111192330
173290585832905859GA67GENIChomozygous111031166
173290772532907726CT76GENIChomozygous111031168
173290813532908136AC64GENIChomozygous111031170
173290816632908167CT67GENIChomozygous111031172
173290838232908383TG72GENIChomozygous111031174
173290951932909520TA67GENIChomozygous111031176
173290974932909750GT60GENICpossibly homozygous111031178