chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7468965468966T19GENICheterozygous403198000
7468965468966TC19GENICheterozygous403198001
7468966468967T19GENICpossibly homozygous403198002
7468966468967TC19GENICheterozygous403198003
7468967468968T19GENICheterozygous403198004
7468967468968TC19GENICheterozygous403198005
7468968468969T19GENICheterozygous403198006
7468968468969TC19GENICheterozygous403198007
7469305469306CA46GENIChomozygous137986742
7469499469500GA42GENIChomozygous146439485
7470462470463CT52GENIChomozygous146439486
7471093471094CT47GENIChomozygous146439487
7471762471763AC53GENIChomozygous146439488
7472253472254TC47GENIChomozygous141924752
7472411472412GA63GENIChomozygous146439489
7472459472460AG50GENIChomozygous146439490
7472459472460AT50GENICheterozygous404076407
7472923472924TC25GENICheterozygous154436658
7472923472924T25GENICpossibly homozygous403198008
7475234475235CT46GENIChomozygous137986749
7477518477519AC52GENIChomozygous146439491
7480959480960AG56GENICheterozygous145181949
7480965480966CT54GENICheterozygous145181950
7481157481158AG44GENIChomozygous137986751