chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2079845887984589CT53GENIChomozygous109235941
2079846407984641AT56GENICpossibly homozygous109085375
2080028758002876CA19GENICheterozygous119767335
2080152498015250GT29GENIChomozygous119767337
2080211968021197AG66GENIChomozygous109085426
2080223998022399G31GENIChomozygous129655997
2080277858027786CA51GENIChomozygous109298656
2080223098022310G3GENIChomozygous130490083
2080246858024686GT48GENIChomozygous109298654
2080307358030736A26GENICheterozygous129656000
2080308278030828GA44GENIChomozygous109298658
2080408418040842AC50GENIChomozygous109235951
2080581998058199GGGAG11GENIChomozygous129656010
2080582038058203G13GENIChomozygous129656011
2080582058058205AG12GENIChomozygous129656012
2080654318065432AG49GENIChomozygous109298660
2080660078066007T8GENIChomozygous129656013
2080677758067776C1GENIChomozygous129656014
2080677808067781T1GENIChomozygous129656015
2080677868067788GA1GENIChomozygous129656016
2080677978067797T1GENIChomozygous129656017
2080681098068110CT5GENIChomozygous109085476
2080752558075255TC22GENIChomozygous130490084
2080873078087308TA12GENIChomozygous124632093
2080873078087307CCG13GENIChomozygous129656025
2080878748087875AG20GENICheterozygous119815318
2080880388088039TA23GENIChomozygous109085510
2080883208088321AG33GENIChomozygous109085512
2080885018088502CG69GENIChomozygous109298662
2080921988092199AG64GENIChomozygous109085518
2080965738096575AA23GENIChomozygous129656031
2080944948094495C21GENICpossibly homozygous132367754
2080930848093085CT52GENIChomozygous109298664
2080947978094798AG58GENIChomozygous109085524
2080480828048084TG35GENIChomozygous132240951
2080873658087370TCTAC11GENIChomozygous132240952
2080961038096104G40GENIChomozygous132240956
2080962428096243A37GENIChomozygous132240957