chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
147860640478606405GT15GENIChomozygous49343268
147860703478607035TC10GENIChomozygous48803673
147860703678607037GC9GENIChomozygous48803674
147860703978607040TC9GENIChomozygous49292005
147860705278607055CCA---5GENIChomozygous48803678
147860746378607464GA40GENIChomozygous49343269
147860951278609513T-15GENIChomozygous48803681
147860952778609528TC16GENIChomozygous48803682
147860953878609539TTC14GENIChomozygous49315599
147860954178609542TTC15GENIChomozygous49343270
147860985378609869TGTGTGTGTGTGTGTG----------------12GENIChomozygous49343271
147861032078610322TT--18GENICpossibly homozygous48803686
147861032178610322T-18GENICheterozygous49331896
147861094578610946GT44GENIChomozygous48803688
147861112678611127TG28GENIChomozygous48803689
147861194278611943AG35GENIChomozygous48803690
147861233578612336AG27GENIChomozygous48803691
147861287078612871GGC20GENIChomozygous49343272
147861302678613027GA30GENIChomozygous49343273
147861355078613551TC29GENIChomozygous48803693
147861451478614520ACACAC------10GENICheterozygous49343274
147861451678614520ACAC----10GENICheterozygous49343275
147861525078615251AC36GENIChomozygous48803700
147861569878615699C-30GENIChomozygous48803701
147861657578616576TC19GENIChomozygous48803702
147861823178618232TC45GENIChomozygous48803711
147861847078618471TC30GENIChomozygous48803714
147861865778618658CT23GENIChomozygous49343276
147862077778620778AAT16GENICheterozygous48803727
147862077778620778AATT16GENICpossibly homozygous49343277
147862183578621836AG24GENIChomozygous48803734
147862671378626714CA48GENIChomozygous48803797
147862733678627337GA22GENIChomozygous49343278
147862774778627753GTCCCT------14GENIChomozygous49343279
147862794178627943AT--10GENIChomozygous49343280
147862802178628022CG23GENIChomozygous48803808