chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147805155147805156TC51GENIChomozygous114047380
5147805333147805334AC53GENIChomozygous114047382
5147805883147805884GA29GENIChomozygous114047384
5147807611147807612TC45GENIChomozygous114047386
5147809187147809188AG39GENIChomozygous114047388
5147809815147809816CG36GENICheterozygous114047390
5147810036147810037AT46GENIChomozygous114047392
5147810187147810188TG47GENIChomozygous114047394
5147810259147810260TG58GENIChomozygous114047396
5147810358147810359GA45GENICpossibly homozygous114047398
5147810632147810633AG28GENICheterozygous114047400
5147810641147810642GA23GENICheterozygous114047402
5147810664147810665AG10GENICheterozygous114047404
5147810747147810748AG53GENICheterozygous114047406
5147811709147811710TC32GENIChomozygous114047408
5147811735147811736TC45GENICpossibly homozygous114047410
5147811883147811884AT52GENIChomozygous114047412