chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261833899261833900AT24GENIChomozygous108630093
1261835253261835254CT20GENIChomozygous108630094
1261836375261836376GA13GENIChomozygous108630095
1261837425261837426AG13GENIChomozygous108630096
1261840651261840652GA13GENIChomozygous108630097
1261841495261841496CT14GENIChomozygous108630098
1261842757261842758TC26GENIChomozygous108630099
1261842876261842877CT19GENIChomozygous108630100
1261844246261844247GA21GENIChomozygous108630101
1261844412261844413GT23GENIChomozygous108630102
1261844541261844542GA31GENIChomozygous108630103
1261843415261843431CTACTGCCCCAGTGCT15GENIChomozygous127507564
1261843614261843619GCACA18GENIChomozygous127507565
1261845379261845380TC18GENIChomozygous108630105
1261845381261845382TC19GENICheterozygous108630106
1261847388261847388AT18GENIChomozygous127507566
1261848342261848343GA18GENIChomozygous108630107
1261849048261849049AT19GENIChomozygous108630108
1261849051261849052AT19GENIChomozygous108630109
1261849670261849671CT17GENIChomozygous108630110