chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207958325207958327TT--5GENIChomozygous688741722
2207958586207958587TC28GENIChomozygous516896742
2207959077207959078GA6GENIChomozygous518517110
2207959081207959082TC5GENIChomozygous518517111
2207959084207959085GA6GENICheterozygous518517112
2207959088207959089CT5GENICheterozygous518517113
2207959089207959090AG5GENICheterozygous518517114
2207959097207959098CT5GENICheterozygous518517115
2207959100207959101AG5GENICheterozygous518517116
2207959185207959186AT5GENIChomozygous518517117
2207959197207959198GA13GENICheterozygous518517118
2207959200207959201AC18GENICheterozygous518517119
2207959204207959205GA20GENICheterozygous518517120
2207959208207959209CT20GENICheterozygous518517121
2207959209207959210AG22GENICheterozygous518517122
2207959217207959218CT31GENICheterozygous518517123
2207959220207959221AG35GENICheterozygous518517124
2207959261207959262AC48GENICheterozygous516896743
2207959277207959278CT43GENICheterozygous516896744
2207959280207959281AG42GENICheterozygous516896745
2207959407207959408TA40GENIChomozygous516896746
2207960148207960149GA27GENICheterozygous518517125
2207960237207960238GA26GENIChomozygous518517126
2207961177207961178AG20GENIChomozygous518517127