chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1420204262020427CA28GENIChomozygous795596382
1420204372020438TC22GENIChomozygous795596383
1420211482021149AG39GENICpossibly homozygous795596384
1420211762021177TC41GENIChomozygous795596385
1420214172021418AG39GENIChomozygous795596386
1420224522022453AG36GENIChomozygous795596387
1420226232022624AG23GENIChomozygous795596388
1420234352023436CT37GENIChomozygous795596389
1420235412023542GA26GENIChomozygous795596390
1420238482023849AG25GENIChomozygous795596391
1420241392024140AG40GENIChomozygous795596392
1420241602024161AG40GENIChomozygous795596393
1420244562024457CT27GENIChomozygous795596394
1420250422025043CT31GENICpossibly homozygous795596395
1420250502025051GA26GENIChomozygous795596396
1420269902026991TC35GENIChomozygous795596397
1420272112027212AG34GENIChomozygous795596398
1420276632027664GA36GENIChomozygous795596399
1420284712028472CT33GENICpossibly homozygous795596400
1420305142030515GA39GENIChomozygous795596401
1420310962031097CT36GENIChomozygous795596402
1420311712031172TC30GENIChomozygous795596403