chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4231265140231265141TC19GENICpossibly homozygous57129343
4231265371231265372GA21GENICpossibly homozygous57129344
4231265501231265502TC14GENICpossibly homozygous57129345
4231265769231265770GA8GENIChomozygous57129346
4231268755231268756CT11GENIChomozygous57129347
4231270073231270074AG15GENICpossibly homozygous57129348
4231270915231270916AC17GENIChomozygous57129349
4231271432231271434TT--2GENICheterozygous57129350
4231271438231271439T-1GENIChomozygous57129351
4231271458231271459C-2GENIChomozygous57129353
4231271548231271549TC8GENIChomozygous57129354
4231272733231272734TC15GENICpossibly homozygous57129355
4231272790231272791CA12GENIChomozygous57129356