chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1247870900247870901A10GENIChomozygous127501544
1247871543247871544AG14GENIChomozygous108603202
1247872344247872345GA9GENIChomozygous108603204
1247873304247873305TC13GENIChomozygous108603205
1247873728247873729CT18GENIChomozygous108775635
1247874000247874000T7GENIChomozygous127501545
1247874001247874002GC6GENIChomozygous120523932
1247874009247874009C8GENIChomozygous127501546
1247874710247874711GA26GENIChomozygous108775636
1247874822247874823CG18GENIChomozygous108603206
1247876249247876250GT23GENIChomozygous108603207
1247877564247877565AG15GENIChomozygous108603208
1247877736247877737TC12GENIChomozygous108603209
1247877755247877756C16GENIChomozygous131265666
1247878686247878691CTCTC4GENIChomozygous132541625
1247878718247878722CTCC2GENIChomozygous127501547
1247879120247879130TGTATGTGTA10GENIChomozygous132541626
1247879418247879419TC6GENIChomozygous132557921
1247879748247879750AA2GENIChomozygous127501556