chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172240790822407909AG14GENIChomozygous110991819
172241179022411791AT24GENIChomozygous110991823
172241564722415648CT11GENIChomozygous111178980
172241570422415705GC15GENIChomozygous111558254
172241691622416917CT11GENIChomozygous110991827
172241782422417825TC34GENIChomozygous111178982
172241934522419346AC22GENIChomozygous110991831
172242025222420253GA16GENIChomozygous110991833
172242291722422918GA19GENIChomozygous110991835
172241901922419020TG5GENIChomozygous111430684
172242183422421835GA13GENIChomozygous125614612
172242524622425247CT23GENIChomozygous111234946
172242820622428207CG9GENICheterozygous110991839
172242848622428487AC24GENIChomozygous110991841
172242860822428609GA16GENIChomozygous111234950
172242978022429781AG10GENIChomozygous110991845
172242987622429877AG6GENIChomozygous111178999
172243073322430734GC5GENIChomozygous110991849
172243105122431052GA7GENIChomozygous125614613
172243173622431737CG15GENIChomozygous111179001
172243194022431941TA15GENIChomozygous125614614
172243324522433246AG13GENIChomozygous111496916
172243329022433291CG10GENIChomozygous110991853
172243329322433294AC12GENIChomozygous110991855
172243363922433640GA23GENIChomozygous125614615
172243524622435247TC13GENIChomozygous110991861
172243831522438316CT20GENIChomozygous110991867