chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214375955214375956TC31GENIChomozygous108532379
1214376175214376175CTT32GENIChomozygous127481169
1214376451214376452A26GENIChomozygous127481170
1214376726214376728CC28GENIChomozygous127481171
1214377125214377126T24GENIChomozygous127481172
1214377502214377503TC21GENIChomozygous108532380
1214377599214377600CA34GENIChomozygous108532381
1214377709214377710TG21GENIChomozygous108532382
1214377935214377936CA23GENIChomozygous108532383
1214378023214378025AC26GENIChomozygous127481173
1214378309214378310CT25GENIChomozygous108532384
1214378393214378394CA11GENIChomozygous121174421
1214378464214378465CT26GENIChomozygous108532385
1214378647214378648GA40GENIChomozygous108532386
1214379430214379431AG26GENIChomozygous108532387
1214379707214379708GC31GENIChomozygous108532388
1214379953214379954AG25GENIChomozygous108532389
1214380033214380034CG16GENIChomozygous108532390
1214380178214380179AG25GENIChomozygous108532391
1214381179214381180CT43GENIChomozygous108532392
1214381761214381762CT17GENIChomozygous108532393
1214381939214381940GT19GENIChomozygous108532394
1214381944214381945GT19GENIChomozygous108532395
1214381954214381962CTTTTTCC19GENIChomozygous127481174
1214382007214382008AG20GENIChomozygous108532396
1214382021214382022C20GENIChomozygous127481175
1214382117214382120TGT22GENIChomozygous127481176
1214382121214382138TGTATGTATGTATGTAT22GENIChomozygous127481177
1214382436214382437GA20GENIChomozygous108532398
1214382582214382583AC23GENIChomozygous108532399
1214382788214382789TC30GENIChomozygous108532400
1214384631214384632GA32GENIChomozygous108532401