chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	44821995	44821996	A	AT	40	GENIC	homozygous	46141616
19	44822028	44822029	T	TA	38	GENIC	homozygous	46141618
19	44822030	44822031	C	A	40	GENIC	homozygous	46141620
19	44822035	44822036	G	A	40	GENIC	homozygous	46141622
19	44822082	44822083	T	A	34	GENIC	homozygous	46141624
19	44822085	44822086	T	-	33	GENIC	homozygous	46141626
19	44822093	44822094	G	A	26	GENIC	homozygous	46141628
19	44822157	44822158	C	A	23	GENIC	homozygous	46141629
19	44822727	44822728	G	C	27	GENIC	homozygous	46141631
19	44822730	44822731	A	G	27	GENIC	homozygous	46141633
19	44822764	44822765	T	-	22	GENIC	homozygous	46141635
19	44822797	44822798	G	T	23	GENIC	homozygous	46141637
19	44822823	44822824	A	AT	22	GENIC	homozygous	46141639
19	44822849	44822850	T	TC	25	GENIC	homozygous	46141641
19	44822877	44822878	G	T	32	GENIC	homozygous	46380520
19	44828497	44828498	G	GGATA	13	GENIC	heterozygous	46212782
19	44828498	44828502	GATA	----	13	GENIC	heterozygous	46212783
19	44835369	44835370	C	-	19	GENIC	homozygous	46141645
19	44850711	44850712	A	G	18	GENIC	homozygous	46141651
19	44856762	44856763	T	-	10	GENIC	heterozygous	46462185
19	44859319	44859323	GTGT	----	13	GENIC	heterozygous	46212784
19	44859321	44859323	GT	--	13	GENIC	heterozygous	46212785
19	44859657	44859659	GT	--	13	GENIC	heterozygous	46406437