chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13149650531496506CG18GENICheterozygous108713985
13149898331498984G9GENICheterozygous132792646
13150165531501656CT14GENICheterozygous130839942
13150121831501219CT11GENICheterozygous132799095
13150403331504034AG11GENICheterozygous132799096
13150408431504085TC10GENICheterozygous130839951
13150448331504484TG12GENICheterozygous132799097
13150749331507494TC19GENICheterozygous120953672
13150756231507563TC16GENICheterozygous120953675
13150757131507572GA16GENICheterozygous120953677
13150757231507573CG16GENICheterozygous132799098
13150761631507617TC12GENICheterozygous132799099
13150762431507625AC14GENICheterozygous132799100
13150772031507721GC11GENICheterozygous132799101
13150772331507724TA12GENICheterozygous127528826
13150357531503576GA9GENICheterozygous127528822
13150853931508539C10GENICheterozygous130814742
13150976831509769TG14GENICheterozygous108714107
13151052531510526GA6GENICheterozygous132799102
13151109831511099AG11GENICheterozygous108714127
13151315731513158CG18GENICheterozygous108714143
13151625131516252GA10GENICheterozygous132799103
13151757731517578AG19GENICheterozygous108714251
13151541831515419CT11GENICheterozygous120660114