chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5169571894169571895A-23INTERGENICheterozygous56465222
5169572826169572827GGTGTA13INTERGENIChomozygous55838215
5169578999169579001TG--14GENICheterozygous56533357
5169594122169594124CA--18GENICheterozygous56465226
5169600987169600988GGTGGGAGTTGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCACACCTCAGCTCCCACCACATTGGTGGC38GENIChomozygous56465227
5169603351169603352TTGGTTAAG9GENIChomozygous55838220
5169603524169603525GT22GENIChomozygous55838221
5169604195169604196AG13GENIChomozygous55838222
5169607079169607080A-12INTERGENICheterozygous56563789
5169608012169608013CCTGTG9INTERGENICheterozygous56555273
5169608019169608025TGTGTG------9INTERGENICheterozygous56646591
5169608072169608073AG15INTERGENICheterozygous56570658
5169612310169612311CCTTCTTCTCCTCCTCCTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTT12INTERGENIChomozygous56364799
5169618897169618899TG--20GENICheterozygous55838227
5169628539169628540TG17GENICpossibly homozygous55838228
5169632376169632377T-10INTERGENICheterozygous55838232
5169634040169634041T-15INTERGENICheterozygous56533358
5169635991169635993CA--4INTERGENICheterozygous56555275
5169637700169637702AC--7INTERGENICheterozygous56465228
5169643285169643287AG--8INTERGENICpossibly homozygous56465229
5169646348169646349AAT16GENICpossibly homozygous55838234
5169650974169650976CT--3GENICheterozygous56465231
5169653216169653217GGA9GENICheterozygous56465232
5169653217169653218A-9GENICheterozygous56465233
5169653559169653560GGCTGGCCTC14GENIChomozygous55838235
5169650968169650976CTCTCTCT--------3GENICheterozygous56687523