chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130090188130090189TG21INTERGENICpossibly homozygous69118886
7130090319130090320TA32INTERGENIChomozygous69118889
7130090326130090327TG33INTERGENIChomozygous69118891
7130090503130090504TC31INTERGENIChomozygous69118894
7130090554130090555GC30INTERGENIChomozygous69118897
7130091070130091071GA40INTERGENIChomozygous69118900
7130091073130091074CT39INTERGENIChomozygous69118903
7130091157130091158GA50INTERGENIChomozygous69118906
7130091158130091159GA50INTERGENIChomozygous69118909
7130091211130091212GA48INTERGENIChomozygous69118911
7130091284130091285GC48INTERGENIChomozygous69118914
7130091346130091347AG41INTERGENIChomozygous69118917
7130091637130091638AG47INTERGENIChomozygous69118919
7130091993130091994AG41INTERGENIChomozygous69118922
7130092371130092372TA35INTERGENIChomozygous69118925
7130092675130092676CT23INTERGENIChomozygous69118928
7130092784130092785TC32INTERGENIChomozygous69118931
7130092934130092935GA28INTERGENIChomozygous69118934
7130092937130092938AT28INTERGENIChomozygous69118937
7130092990130092991TC36INTERGENIChomozygous69118940