chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	43827045	43827045		TCGTCC	5	GENIC	homozygous	133858697
19	43827077	43827077		CTT	6	GENIC	homozygous	133858698
19	43828683	43828689	ACCAAC		22	GENIC	homozygous	133858699
19	43827059	43827059		CTT	4	GENIC	homozygous	129611061
19	43827469	43827469		ATTTATTC	20	GENIC	homozygous	129611063
19	43828128	43828128		AT	17	GENIC	homozygous	129611064
19	43827290	43827291	A	T	10	GENIC	homozygous	109962490
19	43828491	43828492	A	T	19	GENIC	homozygous	109784141
19	43831745	43831746	C	T	16	GENIC	homozygous	109962492
19	43833339	43833340	G	C	20	GENIC	homozygous	109784143
19	43833996	43833997	C	T	21	GENIC	homozygous	109962494
19	43834444	43834445	C	T	20	GENIC	homozygous	109784145
19	43835783	43835783		TGCTACAGT	11	GENIC	homozygous	133858700
19	43836113	43836114	C	T	21	GENIC	homozygous	109708340
19	43839174	43839175	T	C	31	GENIC	homozygous	109784147
19	43842924	43842925	T	C	12	GENIC	homozygous	109784149
19	43845286	43845286		AT	11	GENIC	homozygous	129611068
19	43845609	43845610	G	A	19	GENIC	homozygous	109962496
19	43846743	43846744	A	G	33	GENIC	homozygous	109708364
19	43847410	43847411	T	G	21	GENIC	homozygous	109784151
19	43848102	43848103	C	T	10	GENIC	homozygous	109928814