chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7113467696113467697TC73GENIChomozygous138184434
7113472674113472684GTGTGCGCGC35GENICheterozygous146820234
7113472683113472684CT30GENICheterozygous403222726
7113472681113472682C30GENICpossibly homozygous403222723
7113472681113472682CT30GENICheterozygous403222724
7113472683113472684C30GENICpossibly homozygous403222725
7113473906113473907GA53GENIChomozygous138184435
7113474284113474285AG56GENIChomozygous138184436
7113474902113474903TC81GENIChomozygous138184437
7113476761113476762AG53GENIChomozygous138184438