chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	36956390	36956391	T	TA	18	GENIC	possibly homozygous	46109861
19	36956921	36956922	A	AAGACAGACTGACAGGCAAGACAGACAGAC	27	GENIC	homozygous	46380061
19	36957156	36957157	G	GT	13	GENIC	possibly homozygous	46109863
19	36957481	36957482	A	-	10	GENIC	homozygous	46109864
19	36959068	36959069	G	A	28	GENIC	homozygous	46109865
19	36959832	36959834	AA	--	19	GENIC	possibly homozygous	46109866
19	36959833	36959834	A	-	19	GENIC	heterozygous	46550941
19	36959880	36959881	C	CAG	7	GENIC	heterozygous	46109867
19	36961178	36961179	C	CA	11	GENIC	heterozygous	46249551
19	36961179	36961180	A	-	11	GENIC	heterozygous	46380063
19	36961329	36961330	T	G	25	GENIC	homozygous	46109868
19	36963860	36963861	C	T	27	GENIC	homozygous	46109869
19	36967611	36967612	C	G	25	GENIC	homozygous	46109870
19	36969170	36969175	TTTTT	-----	15	GENIC	heterozygous	46461431
19	36970303	36970304	G	A	19	GENIC	homozygous	46109873
19	36970597	36970598	A	AT	25	GENIC	homozygous	46109874
19	36971204	36971205	T	A	36	GENIC	homozygous	46109875
19	36971707	36971708	C	T	28	GENIC	homozygous	46109876
19	36972313	36972314	G	A	28	GENIC	homozygous	46109877
19	36972955	36972956	C	T	19	GENIC	homozygous	46109878
19	36973529	36973531	TT	--	2	GENIC	heterozygous	46520004
19	36974178	36974179	G	GA	16	GENIC	heterozygous	46403226
19	36974179	36974180	A	-	16	GENIC	heterozygous	46429715
19	36975008	36975012	TATT	----	12	GENIC	homozygous	46109881
19	36976220	36976221	A	G	37	GENIC	homozygous	46109882