chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134874720648747207AG16GENIChomozygous114761326
134875059248750593AG20GENIChomozygous115182200
134875139448751395TC21GENIChomozygous114761328
134875175648751757GC14GENIChomozygous114761330
134875225648752257AG9GENIChomozygous114761332
134875228548752286TG4GENICheterozygous115137017
134875261748752618TC7GENIChomozygous114549617
134875428848754289CG11GENIChomozygous114761334
134875439648754397TG4GENIChomozygous114761336
134875456348754564CG6GENIChomozygous114761338
134875511048755111AG24GENIChomozygous114761340
134875535348755354TC11GENIChomozygous114549618
134875592748755928GA8GENICheterozygous114761346
134875614348756144TA5GENIChomozygous114761348
134875669048756691GA15GENIChomozygous114761350
134875740448757405AG7GENIChomozygous114761352
134875795748757958GA16GENIChomozygous114761354
134875876348758764GA24GENIChomozygous114761356
134875927048759271AG10GENIChomozygous114761358
134875953548759536GA8GENIChomozygous114761360
134875966148759662CT16GENIChomozygous114761364
134875974148759742AG8GENIChomozygous114761366
134876193748761938TC19GENIChomozygous114761368
134876404348764044GT9GENIChomozygous114761370
134876444348764444TC11GENIChomozygous114761372
134876531348765314TA7GENIChomozygous114761374