chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3105057126105057127TA4GENICheterozygous136781567
3105057127105057128CA4GENICheterozygous136781568
3105057129105057130CA4GENICheterozygous146717510
3105057308105057309AG19GENIChomozygous146717511
3105058084105058085TC23GENIChomozygous136781569
3105058159105058160CT21GENIChomozygous146717512
3105058709105058710TC24GENIChomozygous136781572
3105059215105059216AC32GENIChomozygous136781573
3105061705105061706CT29GENIChomozygous146717513
3105061846105061847GA18GENIChomozygous146717514
3105063548105063549AG26GENIChomozygous136781581
3105065006105065007TC26GENIChomozygous136781585
3105065660105065661CT23GENIChomozygous146717515
3105065696105065697AT27GENIChomozygous136781587
3105066309105066310GA26GENIChomozygous146717516
3105067227105067228AG24GENIChomozygous136781589
3105068562105068563C14GENICpossibly homozygous140986154
3105068563105068564CT14GENICpossibly homozygous136781593
3105069995105069996TA29GENIChomozygous146717517
3105070197105070198GA24GENIChomozygous146717518
3105057999105057999C22GENIChomozygous146696111
3105061009105061013CACA6GENIChomozygous136581540
3105067220105067220TTGAC22GENIChomozygous136581542