chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261833899261833900AT54GENIChomozygous108630093
1261835253261835254CT54GENIChomozygous108630094
1261836375261836376GA43GENIChomozygous108630095
1261837425261837426AG49GENIChomozygous108630096
1261840651261840652GA45GENIChomozygous108630097
1261841495261841496CT46GENIChomozygous108630098
1261842757261842758TC48GENIChomozygous108630099
1261842876261842877CT57GENIChomozygous108630100
1261843415261843431CTACTGCCCCAGTGCT38GENIChomozygous127507564
1261843614261843619GCACA33GENIChomozygous127507565
1261844246261844247GA38GENIChomozygous108630101
1261844412261844413GT50GENIChomozygous108630102
1261844541261844542GA55GENIChomozygous108630103
1261847388261847388AT39GENIChomozygous127507566
1261849051261849052AT58GENIChomozygous108630109
1261845379261845380TC21GENICpossibly homozygous108630105
1261845381261845382TC21GENICpossibly homozygous108630106
1261848342261848343GA40GENIChomozygous108630107
1261849048261849049AT57GENIChomozygous108630108
1261849670261849671CT51GENIChomozygous108630110