chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2186116640186116641GA21GENICheterozygous110614023
2186116678186116679CT21GENICheterozygous110165316
2186116743186116744TC25GENICheterozygous110165317
2186116813186116814AG39GENICheterozygous110165318
2186116879186116880GA42GENICheterozygous110165319
2186116901186116902GA46GENICheterozygous110165320
2186116970186116971GA53GENICheterozygous110165321
2186117451186117452CT51GENICheterozygous110165324
2186117533186117534CT40GENICheterozygous110165326
2186117539186117540CT42GENICheterozygous110165327
2186117540186117541AG43GENICheterozygous110165328
2186117560186117561TG51GENICheterozygous110165329
2186117618186117619CT51GENICheterozygous110803232
2186117622186117623TC51GENICheterozygous110165330
2186117653186117654GA46GENICheterozygous110165331
2186123445186123446AG24GENIChomozygous110165336
2186130352186130353AG15GENIChomozygous110990838
2186130747186130748TC22GENIChomozygous110165348
2186130938186130939GA24GENIChomozygous110165349
2186147193186147194TG2GENIChomozygous120242950
2186147196186147197AG1GENIChomozygous120242951
2186186089186186090GA3GENIChomozygous110165454
2186190690186190691TA35GENIChomozygous110165463
2186243497186243498GA21GENIChomozygous111146074
2186244424186244425AG25GENIChomozygous110991079
2186244788186244789CT6GENIChomozygous110991081