chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	44915412	44915413	G	GT	26	GENIC	homozygous	46141702
19	44917076	44917077	T	TAA	41	GENIC	homozygous	46141704
19	44917077	44917078	T	G	41	GENIC	homozygous	46406451
19	44921800	44921801	T	-	14	GENIC	heterozygous	46430452
19	44922082	44922083	A	G	21	GENIC	homozygous	46141706
19	44922084	44922085	A	T	21	GENIC	homozygous	46141708
19	44922107	44922108	A	G	15	GENIC	homozygous	46141709
19	44922113	44922114	A	C	15	GENIC	homozygous	46141711
19	44922117	44922118	A	G	15	GENIC	homozygous	46406453
19	44922119	44922120	A	T	15	GENIC	homozygous	46406455
19	44922121	44922122	C	G	13	GENIC	homozygous	46406457
19	44922123	44922124	G	T	12	GENIC	homozygous	46406459
19	44922145	44922146	G	T	4	GENIC	homozygous	46141713
19	44922147	44922148	A	G	3	GENIC	homozygous	46141715
19	44922155	44922156	G	-	2	GENIC	homozygous	46141719