chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	19354895	19354896	G	A	53	GENIC	homozygous	139889822
16	19355506	19355507	C	T	44	GENIC	homozygous	139889823
16	19355983	19355984	A	G	56	GENIC	homozygous	139889824
16	19356140	19356141	C	T	54	GENIC	homozygous	139889825
16	19356583	19356584	A	G	61	GENIC	homozygous	139889826
16	19357059	19357060	T	A	65	GENIC	homozygous	139889827
16	19357251	19357252	G	A	38	GENIC	possibly homozygous	139889828
16	19357254	19357402	ACACACACATGGTGGAACACACATGGTGGAACACACACATGGTGGAACACACACGGTGGAACACACACATGGTGGAACACACACATGGTGGAACACACACATGGTGGAACACACACACACATGGTGGAACACACACATGGTGGAACAC		43	GENIC	possibly homozygous	139824830
16	19357323	19357324	T	C	43	GENIC	heterozygous	403945335
16	19357277	19357278	T	C	43	GENIC	heterozygous	154990774
16	19357277	19357278	T		43	GENIC	possibly homozygous	403945333
16	19357323	19357324	T		43	GENIC	possibly homozygous	403945334
16	19357484	19357484		ACACACATGGTGGAACACACACATGGTGGA	32	GENIC	possibly homozygous	139824831
16	19359602	19359606	CCAG		38	GENIC	homozygous	139824832
16	19359606	19359607	A	T	40	GENIC	homozygous	139889829
16	19359608	19359609	G	T	40	GENIC	homozygous	139889830
16	19359609	19359610	C	T	40	GENIC	homozygous	139889831
16	19370947	19370948	C	T	41	GENIC	homozygous	139889832
16	19371505	19371506	C	T	46	GENIC	heterozygous	139889833
16	19374573	19374574	T	C	48	GENIC	homozygous	139889834
16	19374920	19374921	G	A	60	GENIC	homozygous	139889835
16	19375799	19375800	T	C	30	GENIC	homozygous	139889836
16	19380996	19380997	A	T	50	GENIC	homozygous	139889837
16	19382086	19382089	TTA		38	GENIC	heterozygous	139824833