chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37649347	37649348	G	A	18	GENIC	homozygous	140452555
19	37649428	37649429	G	A	19	GENIC	homozygous	140452556
19	37649790	37649791	C	T	20	GENIC	homozygous	140452557
19	37652771	37652772	C	T	15	GENIC	homozygous	140452558
19	37654567	37654568	A	C	19	GENIC	homozygous	140452559
19	37658877	37658878	C	G	23	GENIC	homozygous	140452560
19	37659582	37659583	G	A	20	GENIC	homozygous	140452561
19	37659630	37659631	C	T	20	GENIC	homozygous	140452562
19	37664889	37664890	G	A	17	GENIC	homozygous	140452563
19	37665291	37665292	C	G	19	GENIC	homozygous	140452564
19	37665950	37665951	T	G	12	GENIC	homozygous	140452565
19	37666283	37666284	G	A	28	GENIC	homozygous	140452566
19	37666306	37666307	A	G	23	GENIC	homozygous	140452567
19	37668354	37668355	T	C	18	GENIC	homozygous	140452568
19	37669866	37669867	A	G	19	GENIC	homozygous	140452569
19	37654476	37654504	AATAAAGGGAAGCTCTTGTTTTCAGGAA		13	GENIC	homozygous	140388597
19	37656543	37656546	CTC		17	GENIC	homozygous	140388598
19	37664769	37664771	TA		17	GENIC	possibly homozygous	140388599