chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
29351931393519314CG10GENIChomozygous110720298
29351955193519552CT32GENIChomozygous110720299
29351977693519777GT21GENIChomozygous110720300
29352185693521857TC28GENIChomozygous109920356
29352203693522037TG29GENIChomozygous110720301
29352387393523874CT30GENIChomozygous109920364
29352451593524516AG30GENIChomozygous110720302
29352459293524593CT22GENIChomozygous110720303
29352540493525405TC30GENIChomozygous109920370
29352671593526716GA30GENIChomozygous110720304
29352807693528077AG35GENIChomozygous110720305
29352857193528572GA57GENIChomozygous110720306
29352878193528782CT48GENIChomozygous110720307
29352919293529193GA29GENIChomozygous110720308
29352929793529298GA36GENIChomozygous110720309
29352959793529598CT29GENIChomozygous110720310
29352984993529850AG31GENIChomozygous110720311
29353002293530023CT35GENIChomozygous110720312
29353091493530915AC33GENIChomozygous110720313
29353120093531201TG25GENIChomozygous110720314
29353125793531258GA34GENIChomozygous110720315
29353140393531404AG33GENIChomozygous110720316
29353152693531527TG33GENIChomozygous110720317
29353156293531563GT33GENIChomozygous109920374
29353162593531626TC35GENIChomozygous109920376
29353304793533048TA30GENIChomozygous110720318
29353305493533055AT28GENIChomozygous109920380
29353340593533406CT31GENIChomozygous110720319
29353395093533951AG9GENIChomozygous110720320
29353545493535455CT22GENIChomozygous110720321
29353665493536655AG23GENIChomozygous109920392
29353738293537383TC28GENIChomozygous109920396
29353783793537838AG32GENIChomozygous109920398
29353833893538339AG28GENIChomozygous109920402
29353838493538385CG38GENIChomozygous110720322
29353839193538392GA36GENIChomozygous110720323
29353842093538421GA30GENIChomozygous110720324
29353851793538518CA22GENIChomozygous110720325
29353983493539835AT12GENIChomozygous109920406
29354049793540498GA33GENIChomozygous109920407
29354087093540871CT26GENIChomozygous110720326
29353894993538950CT16GENICheterozygous120302956