chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228438750228438751GGGC34GENIChomozygous61603831
1228439376228439377GA21GENIChomozygous61603832
1228439518228439519TTG42GENIChomozygous61603833
1228439956228439957AG24GENIChomozygous61603834
1228440082228440087AAAAC-----18GENIChomozygous61603835
1228440375228440376GT26GENIChomozygous61603836
1228440994228440995CG21GENIChomozygous61603837
1228441088228441089CCCAAA17GENIChomozygous61603838
1228441387228441388TC27GENIChomozygous61603840
1228441545228441546AC45GENIChomozygous61603841
1228442016228442017CT36GENIChomozygous61603842
1228442109228442110CG22GENIChomozygous61603843
1228443114228443115GA22GENICheterozygous61107076
1228448389228448390AT5GENIChomozygous61603844
1228448723228448724AT18GENIChomozygous61603845
1228449246228449247TC33GENIChomozygous61603846
1228449416228449417AAT22GENIChomozygous61603847
1228449428228449429TC27GENICpossibly homozygous61603848
1228449704228449705CT23GENIChomozygous61603849
1228450466228450467AATTTCCCTTT22GENIChomozygous61603850