chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1247870900247870901A29GENIChomozygous127501544
1247871143247871144G39GENICpossibly homozygous134653344
1247871147247871156GTGTGTGTG34GENICpossibly homozygous134653345
1247871543247871544AG53GENIChomozygous108603202
1247872221247872222GA48GENIChomozygous120903170
1247872344247872345GA54GENIChomozygous108603204
1247872744247872745CT63GENIChomozygous120903171
1247873304247873305TC57GENIChomozygous108603205
1247874000247874000T22GENIChomozygous127501545
1247874009247874009C26GENIChomozygous127501546
1247874500247874501TG55GENIChomozygous120903172
1247874822247874823CG43GENIChomozygous108603206
1247875230247875231GC60GENIChomozygous120903173
1247876249247876250GT58GENIChomozygous108603207
1247877564247877565AG53GENIChomozygous108603208
1247877658247877658A49GENIChomozygous134653353
1247877736247877737TC43GENIChomozygous108603209
1247877755247877756C38GENIChomozygous131265666
1247878145247878146AG54GENICpossibly homozygous120903174
1247878302247878303CT42GENIChomozygous120903175
1247878650247878652TC16GENIChomozygous134653354
1247878659247878660CG16GENIChomozygous120903176
1247878718247878722CTCC18GENIChomozygous127501547
1247879431247879432TA12GENIChomozygous134662827
1247879732247879733AG5GENIChomozygous133531643
1247879748247879750AA2GENIChomozygous127501556
1247879838247879839G4GENIChomozygous129845848
1247879797247879798TC4GENIChomozygous135147392
1247874001247874002GC22GENIChomozygous120523932
1247879559247879560AG10GENIChomozygous127583802
1247879687247879688GA8GENIChomozygous127583803
1247879693247879694TC6GENIChomozygous127583804
1247879787247879788TG4GENIChomozygous127583805