chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5169572826169572827GGTGTA10INTERGENICpossibly homozygous55838215
5169578998169578999CCTG25GENICheterozygous55838216
5169578999169579001TG--25GENICheterozygous56533357
5169581132169581134GT--5GENICheterozygous56465224
5169594122169594124CA--16GENICheterozygous56465226
5169600987169600988GGTGGGAGTTGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCACACCTCAGCTCCCACCACATTGGTGGC30GENIChomozygous56465227
5169603351169603352TTGGTTAAG9GENIChomozygous55838220
5169603524169603525GT18GENIChomozygous55838221
5169604195169604196AG31GENIChomozygous55838222
5169612310169612311CCTTCTTCTCCTCCTCCTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTT5INTERGENIChomozygous56364799
5169628539169628540TG23GENICpossibly homozygous55838228
5169635707169635709GG--12INTERGENICheterozygous56085827
5169635708169635709G-12INTERGENICheterozygous55838233
5169635991169635993CA--4INTERGENICheterozygous56555275
5169637700169637702AC--9INTERGENICheterozygous56465228
5169643285169643287AG--9INTERGENICheterozygous56465229
5169648825169648826TTA17GENICheterozygous56496804
5169648826169648827A-17GENICheterozygous55948323
5169650968169650976CTCTCTCT--------3GENICheterozygous56687523
5169650974169650976CT--3GENICheterozygous56465231
5169653559169653560GGCTGGCCTC23GENIChomozygous55838235