chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37173627	37173628	G	A	25	GENIC	homozygous	46110108
19	37174112	37174113	C	T	21	GENIC	homozygous	46110109
19	37174294	37174295	T	TC	18	GENIC	homozygous	46110110
19	37176296	37176297	G	A	14	GENIC	possibly homozygous	46110111
19	37176386	37176387	C	CT	4	GENIC	heterozygous	46110112
19	37176605	37176606	A	C	14	GENIC	homozygous	46110113
19	37178111	37178112	G	T	2	GENIC	homozygous	46110118
19	37178182	37178183	A	G	13	GENIC	homozygous	46110119
19	37178248	37178249	C	T	9	GENIC	heterozygous	46110120
19	37178851	37178852	G	-	13	GENIC	homozygous	46110122
19	37181876	37181877	A	G	21	GENIC	homozygous	46110129
19	37184099	37184100	G	T	8	GENIC	possibly homozygous	46110130
19	37186435	37186436	C	G	10	GENIC	homozygous	46110133
19	37188051	37188052	G	A	13	GENIC	homozygous	46110135
19	37188161	37188162	T	C	15	GENIC	heterozygous	46110136
19	37189201	37189202	C	T	14	GENIC	possibly homozygous	46110137
19	37189336	37189337	T	C	28	GENIC	possibly homozygous	46110138
19	37190952	37190953	T	C	12	GENIC	heterozygous	46110139