chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1154478692154478693TG10GENIChomozygous108317312
1154479672154479673AG19GENIChomozygous108317316
1154479938154479939CA24GENIChomozygous108317317
1154480020154480021TG35GENIChomozygous108317319
1154480796154480797CT34GENIChomozygous108317321
1154481274154481275CA26GENIChomozygous109519620
1154481895154481896GA25GENIChomozygous109519621
1154481967154481968AT14GENIChomozygous108317327
1154482018154482019TC17GENIChomozygous108317329
1154482769154482770AG36GENIChomozygous108317331
1154482773154482774TC36GENIChomozygous108317333
1154483272154483273CT11GENIChomozygous108317335
1154483837154483838AG27GENIChomozygous108317337
1154483840154483841CT27GENIChomozygous108317339
1154484208154484209CG20GENIChomozygous108317341
1154485627154485628TC16GENIChomozygous108317347
1154485706154485707GA15GENIChomozygous108317349
1154486088154486089GA20GENIChomozygous108317351
1154486444154486445TC13GENIChomozygous108317353
1154496926154496927GA26GENIChomozygous108317359
1154497243154497244TC24GENIChomozygous108317363
1154500637154500638AG17GENIChomozygous108317368
1154501891154501892TC34GENIChomozygous109519625
1154501972154501973GA26GENIChomozygous108317370
1154502828154502829TG26GENIChomozygous109519626
1154502986154502987CT26GENIChomozygous108317376
1154505302154505303CT15GENIChomozygous109519630
1154506593154506594TC31GENIChomozygous108317382