chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1165516385165516386TC17GENIChomozygous974619196
1165516967165516968CT11GENIChomozygous974619197
1165518186165518187CT16GENIChomozygous974619198
1165518808165518809CT36GENIChomozygous974619199
1165519206165519207AT8GENICheterozygous974619200
1165519247165519248GA8GENIChomozygous974619201
1165519823165519824TC23GENICpossibly homozygous974619202
1165519873165519874CT16GENIChomozygous974619203
1165520032165520033CT12GENIChomozygous974619204
1165520851165520852GA25GENIChomozygous974619205
1165522389165522390CT30GENIChomozygous974619206
1165522405165522406CT32GENIChomozygous974619207
1165522406165522407CG32GENIChomozygous974619208
1165525629165525630TC13GENIChomozygous974619209
1165525770165525771TC10GENIChomozygous974619210
1165527324165527325CA15GENIChomozygous974619211
1165527481165527482AG15GENIChomozygous974619212
1165527837165527838AT12GENICheterozygous974619213
1165527942165527943CT11GENIChomozygous974619214
1165528020165528021CA11GENIChomozygous974619215
1165528448165528449CG30GENIChomozygous974619216
1165528468165528469TG23GENIChomozygous974619217
1165528554165528555TC21GENIChomozygous974619218
1165528709165528710CG36GENIChomozygous974619219
1165528792165528793AT26GENIChomozygous974619220
1165528959165528960AG34GENIChomozygous974619221
1165529106165529107GA26GENIChomozygous974619222
1165529198165529199CT11GENIChomozygous974619223