chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91915073319150734TC8GENIChomozygous117273105
91915074119150742TG6GENIChomozygous117273106
91915074219150743AC6GENIChomozygous117273107
91915075019150750T4GENIChomozygous128686648
91915075219150753AT5GENIChomozygous117465034
91915075519150756T5GENIChomozygous128686649
91915076219150763GC5GENIChomozygous117273108
91915076919150770GC6GENIChomozygous117273109
91915077019150771GC6GENIChomozygous117273110
91915077319150774TC6GENIChomozygous117273111
91915077819150778C6GENIChomozygous128686650
91917485419174855GA2GENIChomozygous117273175
91917490719174908GA14GENICheterozygous117488051
91917504419175044C13GENICheterozygous128686663
91917512519175126GA4GENICheterozygous123131891
91917512719175128CT4GENICheterozygous123131892
91916928419169285T6GENIChomozygous130377279