chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13114826267114826269GT--16GENICheterozygous50566901
13114826741114826747GGGTTC------16GENICheterozygous50537003
13114826743114826744G-16GENICpossibly homozygous49882079
13114832856114832857AAT3GENICheterozygous49882082
13114838019114838020AC13GENIChomozygous50537007
13114838074114838075CT24GENIChomozygous49882085
13114838077114838078TG26GENIChomozygous49882086
13114838088114838089GT28GENIChomozygous49882087
13114838092114838093GA28GENIChomozygous49882088
13114838116114838117TG17GENIChomozygous49882089
13114838127114838128GT14GENIChomozygous49882090
13114838131114838132GT14GENIChomozygous49882091
13114838133114838134CT14GENIChomozygous49882092
13114838140114838141GT15GENIChomozygous49882093
13114838142114838143AT15GENIChomozygous49882094
13114838144114838145GT15GENIChomozygous49882095
13114838148114838149GT19GENIChomozygous49882096
13114838152114838153GT21GENIChomozygous49882097
13114869281114869287TCTCTC------12GENICheterozygous50416752
13114869949114869955CACACA------11GENICheterozygous50613483
13114838011114838012A-8GENICheterozygous50613481
13114838013114838016TTA---8GENICheterozygous50613482
13114869951114869955CACA----11GENICheterozygous50613484