chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214286276214286277TA52GENICpossibly homozygous778740768
1214286351214286352AG41GENICheterozygous778740769
1214287736214287737GA63GENICheterozygous778740770
1214287745214287746AG66GENICheterozygous778740771
1214288462214288463GA40GENICheterozygous778740772
1214291148214291149AG47GENIChomozygous778740773
1214291223214291224GA50GENICpossibly homozygous778740774
1214293084214293085AG40GENIChomozygous778740775
1214296633214296634TC54GENIChomozygous778740776
1214299976214299977CT74GENIChomozygous778740777
1214301593214301594TC74GENIChomozygous778740778
1214302573214302574CT62GENIChomozygous778740779
1214308425214308426GT42GENICheterozygous778740780
1214311167214311168AG57GENIChomozygous778740781
1214313215214313216TA51GENIChomozygous778740782
1214313464214313465TC63GENIChomozygous778740783