chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1217699853217699854TA4GENICheterozygous125378398
1217701279217701280AG25GENIChomozygous108537189
1217704208217704209GA14GENIChomozygous108537194
1217704899217704900TC5GENIChomozygous108537195
1217706317217706318GA7GENIChomozygous109367121
1217706880217706881AG15GENIChomozygous108537198
1217707359217707360CA7GENIChomozygous108769943
1217708747217708748AG10GENIChomozygous108537200
1217709496217709497TC16GENIChomozygous108537201
1217709841217709842CG9GENIChomozygous108537202
1217709943217709944CG8GENIChomozygous109367122
1217711370217711371AG10GENIChomozygous109367123
1217712291217712292GC16GENIChomozygous125308807
1217712422217712423TG16GENIChomozygous108537205
1217713822217713823TC17GENIChomozygous108537206
1217715616217715617GT20GENIChomozygous108537207
1217715851217715852TC5GENIChomozygous108537209
1217716152217716153GA11GENIChomozygous108537210
1217716560217716561CT18GENIChomozygous108537211
1217716836217716837AG17GENIChomozygous108537212
1217717248217717249GA19GENIChomozygous109367124
1217717633217717634AC18GENIChomozygous108537213
1217719193217719194TC11GENIChomozygous108537214
1217720938217720939GA20GENIChomozygous109367125
1217721904217721905CT19GENIChomozygous108993163
1217722469217722470GA14GENIChomozygous108537216
1217723115217723116TC12GENIChomozygous108537217
1217723780217723781AG11GENIChomozygous108537218
1217725198217725199TG13GENIChomozygous108537220
1217727875217727876TA12GENIChomozygous108993165
1217729283217729284AC6GENIChomozygous108537223
1217732792217732793CT21GENIChomozygous109367127
1217735052217735053TG17GENIChomozygous109367131
1217735474217735475TA21GENIChomozygous108537225
1217735543217735544AT23GENIChomozygous109367132