chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7930825930826AG19GENIChomozygous137987100
7930869930870GA21GENIChomozygous146439608
7932499932500CT23GENIChomozygous146439609
7933099933100CA19GENIChomozygous146439611
7933143933144TC20GENIChomozygous146439612
7933902933903GA19GENIChomozygous146439613
7935308935309AG20GENIChomozygous137987105
7937756937757AG31GENIChomozygous137987107
7938338938339AC13GENICpossibly homozygous154424539
7938620938621TA21GENIChomozygous146439615
7938838938839TC18GENIChomozygous137987109
7939117939118CT19GENIChomozygous146439616
7941102941103TC23GENIChomozygous137987110
7941277941278GT21GENIChomozygous137987111
7935473935473C19GENIChomozygous137932350
7941713941714C14GENIChomozygous137932352
7934136934136TTT8GENIChomozygous146434050
7938620938620A21GENIChomozygous146434051
7940487940489CA14GENIChomozygous137932351
7938337938338A13GENICpossibly homozygous403198119
7938337938338AC13GENICheterozygous403198120
7938338938339A13GENICheterozygous403198121
7942437942438AG14GENIChomozygous137987112
7944232944233A18GENIChomozygous146434052
7944492944493GC18GENICpossibly homozygous146439618