chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106377610663776107GC6GENICheterozygous976572479
106377622363776224AG8GENIChomozygous976572480
106377820363778204CA22GENIChomozygous976572481
106378025263780253GT27GENIChomozygous976572482
106378025363780254TG27GENIChomozygous976572483
106378207463782075TC19GENIChomozygous976572484
106378403763784038CG26GENIChomozygous976572485
106378473463784735AT20GENIChomozygous976572486
106378485563784856GA20GENIChomozygous976572487
106378928963789290TC31GENIChomozygous976572488
106378943963789440GT34GENIChomozygous976572489
106379279063792791CT13GENIChomozygous976572490
106379443963794440TC4GENIChomozygous976572491
106379444063794441TC4GENIChomozygous976572492
106379449263794493AC10GENIChomozygous976572493
106379451963794520GC9GENIChomozygous976572494
106379453263794533GC8GENIChomozygous976572495
106379474163794742GC14GENIChomozygous976572496
106379483063794831TG18GENIChomozygous976572497
106379501463795015TC21GENIChomozygous976572498