chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4176511474176511483GATATCTCG---------16INTERGENIChomozygous57015636
4176511647176511648GC40INTERGENIChomozygous57854917
4176511744176511745CCT45INTERGENIChomozygous57854918
4176511795176511796GT52INTERGENIChomozygous57854919
4176512186176512187GA51INTERGENIChomozygous57854920
4176512419176512420TG39INTERGENIChomozygous57854921
4176512517176512518TC28INTERGENIChomozygous57854922
4176512555176512556AG17INTERGENIChomozygous57854923
4176512987176512988AG47INTERGENIChomozygous57854924
4176513560176513561CT43INTERGENIChomozygous57854925
4176513740176513741GC49INTERGENIChomozygous57854926
4176513832176513833AC46INTERGENICpossibly homozygous57854927
4176513960176513961AC45INTERGENICpossibly homozygous57854928
4176514170176514173AGT---48INTERGENIChomozygous57854929
4176514666176514667GGA48INTERGENIChomozygous57854930
4176515443176515444T-43INTERGENIChomozygous57854931
4176515472176515473CT45INTERGENIChomozygous57854932
4176515684176515685CT53INTERGENIChomozygous57854933
4176515691176515692TA54INTERGENIChomozygous57854934
4176516114176516115AG55INTERGENIChomozygous57854935
4176516870176516871TTCACA11INTERGENIChomozygous57744260
4176517029176517030CA40INTERGENIChomozygous57854936
4176517571176517572TTCTGTTA27INTERGENIChomozygous57015637
4176517574176517575GGT28INTERGENICpossibly homozygous57015638
4176517577176517578CCTGT25INTERGENICpossibly homozygous57015639
4176517745176517746TA43INTERGENIChomozygous57854937