chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106658704766587048AG8GENICheterozygous126385369
106658714766587148CT4GENICheterozygous126409505
106658719966587200CT6GENIChomozygous126409506
106658725266587253TC11GENICheterozygous126385371
106658733366587334AC24GENIChomozygous116620752
106658749366587494CT15GENIChomozygous116620754
106658807666588077AG22GENIChomozygous116620756
106658820866588209AT20GENIChomozygous116620758
106658892566588926TC20GENIChomozygous116620760
106658942466589425AG25GENIChomozygous116620762
106658957066589571TC22GENIChomozygous116620764
106659017766590178TC16GENICheterozygous126385372
106659114766591148CT15GENIChomozygous116620766
106659314666593147TC16GENIChomozygous116620768
106658865566588656TC11GENIChomozygous116793901
106659010666590107TC27GENICheterozygous116793903
106659174466591745GA5GENIChomozygous116793905
106659256366592564TG13GENICheterozygous126461126
106659416966594170CT5GENIChomozygous116620770
106659438766594388TC14GENIChomozygous116620772
106659441466594415TA8GENIChomozygous116620774
106659494866594949AT23GENIChomozygous116620776
106659566266595663AC10GENICheterozygous126422585
106659570066595701TC12GENICheterozygous126385373
106659570966595710AG14GENICheterozygous126385374
106659574166595742TC10GENICheterozygous126409509
106659576766595768CG10GENICheterozygous126385375
106659618466596185GC12GENIChomozygous116620780
106659724266597243TA11GENICheterozygous126422587
106659726866597269CT26GENICheterozygous126422589
106659804966598050CT14GENIChomozygous116620782
106659961366599614AT5GENIChomozygous116620784
106660038166600382GA23GENIChomozygous116620786
106660102466601025AC12GENIChomozygous116793907
106660133366601334CG8GENIChomozygous116620790
106660158666601587AG4GENIChomozygous118104259
106660247666602477CA14GENIChomozygous116620792
106660248166602482TC12GENIChomozygous116620794
106660289466602895GT9GENICheterozygous116620796
106660290866602909CT12GENICheterozygous126409510
106659478266594783AG3GENICheterozygous126488971