chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15106250888106250889TC22GENIChomozygous112638491
15106252006106252007CT29GENIChomozygous112638493
15106253857106253858CT26GENICpossibly homozygous112638496
15106255574106255575GA3GENIChomozygous112638498
15106255576106255577GA3GENIChomozygous112638500
15106256264106256265AT17GENIChomozygous112638502
15106260251106260252AG25GENIChomozygous112638504
15106260287106260288AG32GENIChomozygous112638506
15106261697106261698GA19GENIChomozygous112638508
15106265212106265213AG29GENIChomozygous112638510
15106267051106267052AG31GENIChomozygous112638512
15106268060106268061AC25GENIChomozygous112638516
15106268369106268370AG32GENIChomozygous112638518
15106268580106268581TC37GENIChomozygous112638522
15106268718106268719TC30GENICpossibly homozygous112638524
15106269108106269109TA23GENIChomozygous112638526
15106269213106269214AG26GENIChomozygous112638528
15106271948106271949CT47GENICpossibly homozygous112638530
15106273559106273560TC31GENIChomozygous112638532
15106273597106273598CT26GENIChomozygous112638534
15106274075106274076TC36GENIChomozygous112638536
15106274752106274753GA21GENIChomozygous112638538
15106274864106274865TC35GENIChomozygous112638540
15106277818106277819GA23GENIChomozygous112638543
15106278747106278748TC28GENIChomozygous112638545
15106278839106278840TC20GENIChomozygous112638547
15106279795106279796TG31GENIChomozygous112638549
15106280452106280453TA17GENIChomozygous112638551
15106281028106281029TC18GENIChomozygous112638553
15106283373106283374AG31GENICpossibly homozygous112638555
15106283563106283564GA20GENIChomozygous112638557
15106284330106284331GT36GENIChomozygous112638559
15106284332106284333TC34GENIChomozygous112638561
15106285900106285901GT27GENIChomozygous112638563
15106289545106289546AG19GENIChomozygous112638565
15106290506106290507AG25GENIChomozygous112638567
15106291086106291087AT16GENICpossibly homozygous112638569
15106288416106288417AG19GENIChomozygous112767629