chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191025781610257817CA41GENIChomozygous140403496
191025839910258399GA30GENIChomozygous140376310
191025874910258749AAGGCTGGAGACTGGG41GENIChomozygous140376311
191025890410258905TC37GENIChomozygous140403497
191025942810259428TCTGTGTGTGTG20GENICheterozygous147376324
191025980010259801TG29GENIChomozygous140403499
191025993210259933TG30GENIChomozygous140403500
191026010410260105AG42GENIChomozygous140403501
191026047010260471T36GENIChomozygous140376313
191026055510260556CT25GENIChomozygous147377968
191025871010258711GA43GENIChomozygous148980836
191026134810261349AG38GENIChomozygous140403504
191026238610262387AG26GENIChomozygous140403506
191026276210262763CT55GENIChomozygous140403507
191026341210263413TC59GENIChomozygous140403508
191026394210263943AG51GENIChomozygous140403509
191026397810263979TC46GENIChomozygous140403510
191026410510264106CT44GENIChomozygous147377969
191026173910261740TC17GENIChomozygous148980837
191026145910261460CT39GENIChomozygous148794641