chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	36022438	36022439	C	T	13	GENIC	homozygous	46490464
19	36022658	36022659	T	C	8	GENIC	homozygous	46106556
19	36023948	36023949	C	CG	14	GENIC	homozygous	46490466
19	36024224	36024225	C	CTG	22	GENIC	homozygous	46106562
19	36025100	36025101	C	T	19	GENIC	possibly homozygous	46490468
19	36027244	36027245	C	T	24	GENIC	possibly homozygous	46490470
19	36027738	36027739	T	C	7	GENIC	homozygous	46490472
19	36027883	36027884	C	T	5	GENIC	heterozygous	46490474
19	36031437	36031438	T	C	20	GENIC	homozygous	46490476
19	36032484	36032485	C	T	14	GENIC	possibly homozygous	46106574
19	36034557	36034558	T	G	13	GENIC	homozygous	46490478
19	36036242	36036243	A	G	13	GENIC	homozygous	46490480
19	36040181	36040182	A	G	27	GENIC	homozygous	46106584
19	36043278	36043279	T	C	11	GENIC	heterozygous	46106590
19	36043540	36043543	CTC	---	12	GENIC	homozygous	46490482
19	36043608	36043609	T	C	18	GENIC	possibly homozygous	46106594
19	36044499	36044500	G	A	21	GENIC	homozygous	46490484
19	36044593	36044594	G	-	9	GENIC	homozygous	46106600