chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121692033216920333CT11GENICheterozygous50880357
121696690516966906GA15GENICheterozygous50924618
121701135217011353AT32GENICheterozygous50717621
121701643317016434GA38GENICheterozygous50083153
121702062517020626CT14GENICheterozygous50083170
121702934217029343TC43GENICheterozygous50083250
121702941317029414GA47GENICheterozygous50083252
121702959817029599CT41GENICheterozygous50083254
121705018417050185G-9GENICheterozygous50083394
121705018817050189CCA11GENICheterozygous50083396
121705020617050207GT11GENICheterozygous50083398
121709577217095773A-24GENICheterozygous50083574
121712234117122342AG25GENICheterozygous50083762
121714165517141656TC19GENICheterozygous50083967
121714168117141682AG22GENICheterozygous50083969
121716076217160763TC40GENICheterozygous50800204
121717774417177745TC10GENICheterozygous50084102
121718640017186401CT38GENICheterozygous50800332
121718647117186472CCT35GENICheterozygous50800334
121720469417204695AG23GENICheterozygous50084314
121720472317204724GGA20GENICheterozygous50588048
121721051417210515CCG79GENICheterozygous50084394
121722356917223570AG102GENICheterozygous50084484
121725496517254966CT24GENICheterozygous50924996
121725564717255648T-37GENICheterozygous50084585
121727438617274387CA10GENICheterozygous50822959
121731681617316817GGA23GENICheterozygous50925105
121733881417338815AG34GENICheterozygous50925170
121735985017359851CG118GENICheterozygous50880842
121736003917360040TC59GENICheterozygous50718448
121741743417417435TTA38GENICheterozygous50085354