chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1768410766841077AG8GENIChomozygous110941879
1768448166844817GA10GENIChomozygous110941881
1768459876845988CA20GENIChomozygous110941883
1768460896846090CT13GENIChomozygous110941885
1768472086847209CT25GENIChomozygous110941887
1768479016847902AG24GENIChomozygous110941889
1768489166848917TC18GENIChomozygous110941891
1768503246850325GA26GENIChomozygous110941894
1768506806850681TC26GENIChomozygous110941896
1768508556850856CG7GENIChomozygous110941898
1768508776850878TC6GENIChomozygous110941900
1768536496853650CT25GENIChomozygous110941902
1768548616854862TC24GENIChomozygous110941904
1768590006859001GA25GENIChomozygous110941910
1768605366860537GA33GENIChomozygous110941912
1768615516861552GA21GENIChomozygous110941914
1768642076864208GA22GENIChomozygous110941916
1768645316864532GA27GENIChomozygous110941918
1768670876867088TG32GENIChomozygous110941920
1768671096867110GA36GENIChomozygous110941922
1768676826867683GA16GENIChomozygous110941924
1768687376868738TA19GENIChomozygous110941925
1768717576871758TC20GENIChomozygous110941927
1768724816872482GC19GENIChomozygous110941930
1768725166872517GC24GENIChomozygous110941932
1768733256873326TG19GENIChomozygous110941934
1768734936873494TC27GENIChomozygous110941936
1768758816875882GA16GENIChomozygous110941938
1768779896877990TC18GENIChomozygous110941940