chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37173627	37173628	G	A	39	GENIC	homozygous	46110108
19	37174112	37174113	C	T	18	GENIC	homozygous	46110109
19	37174294	37174295	T	TC	27	GENIC	possibly homozygous	46110110
19	37176296	37176297	G	A	22	GENIC	homozygous	46110111
19	37176386	37176387	C	CT	7	GENIC	possibly homozygous	46110112
19	37176605	37176606	A	C	28	GENIC	homozygous	46110113
19	37177408	37177409	T	TTGTGTGTGTG	12	GENIC	homozygous	46461544
19	37178105	37178106	G	GT	7	GENIC	homozygous	46461546
19	37178111	37178112	G	T	9	GENIC	homozygous	46110118
19	37178182	37178183	A	G	13	GENIC	homozygous	46110119
19	37178248	37178249	C	T	18	GENIC	homozygous	46110120
19	37178376	37178377	T	C	19	GENIC	homozygous	46110121
19	37178851	37178852	G	-	27	GENIC	homozygous	46110122
19	37180728	37180729	A	-	2	GENIC	heterozygous	46110125
19	37181876	37181877	A	G	60	GENIC	homozygous	46110129
19	37184099	37184100	G	T	21	GENIC	homozygous	46110130
19	37184490	37184491	C	T	26	GENIC	homozygous	46461548
19	37184497	37184498	G	GCACACACACA	19	GENIC	heterozygous	46461551
19	37184497	37184498	G	GCACACACACACA	19	GENIC	heterozygous	46461553
19	37184497	37184498	G	GCACACACACACACA	19	GENIC	heterozygous	46461555
19	37186435	37186436	C	G	6	GENIC	homozygous	46110133
19	37186534	37186535	A	G	11	GENIC	possibly homozygous	46110134
19	37187070	37187071	A	T	13	GENIC	heterozygous	46461557
19	37188051	37188052	G	A	26	GENIC	homozygous	46110135
19	37188161	37188162	T	C	19	GENIC	homozygous	46110136
19	37189201	37189202	C	T	10	GENIC	homozygous	46110137
19	37189336	37189337	T	C	27	GENIC	homozygous	46110138
19	37190952	37190953	T	C	39	GENIC	homozygous	46110139