chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	68314070	68314071	C	CA	29	GENIC	homozygous	46301299
19	68314388	68314389	A	G	41	GENIC	homozygous	46301300
19	68314605	68314606	G	A	58	GENIC	homozygous	46196617
19	68314644	68314645	T	C	52	GENIC	homozygous	46196618
19	68315539	68315540	G	T	36	GENIC	homozygous	46196620
19	68316209	68316210	G	A	28	GENIC	homozygous	46301301
19	68317652	68317653	G	T	21	GENIC	homozygous	46301302
19	68317659	68317660	A	T	23	GENIC	homozygous	46301303
19	68318399	68318400	C	T	45	GENIC	homozygous	46196622
19	68318483	68318484	C	T	44	GENIC	homozygous	46301304
19	68318576	68318577	A	G	29	GENIC	homozygous	46196623
19	68319337	68319338	C	T	32	GENIC	homozygous	46196625
19	68319767	68319768	G	GGACACCCTCCCTGCT	25	GENIC	homozygous	46196627
19	68320091	68320092	T	C	26	GENIC	homozygous	46301305
19	68321105	68321106	T	TTGTGTG	3	GENIC	homozygous	46415554
19	68322765	68322779	TGAGATAACTTTTT	--------------	29	GENIC	homozygous	46301306
19	68322948	68322949	A	T	25	GENIC	homozygous	46301307
19	68323545	68323546	T	C	26	GENIC	homozygous	46301308
19	68323764	68323765	T	C	38	GENIC	homozygous	46301309
19	68324419	68324420	T	A	37	GENIC	homozygous	46301310
19	68325046	68325047	T	TG	20	GENIC	possibly homozygous	46301311
19	68325064	68325067	AAA	---	22	GENIC	possibly homozygous	46301312
19	68325065	68325067	AA	--	22	GENIC	heterozygous	46415556
19	68325493	68325494	C	CT	11	GENIC	possibly homozygous	46415558
19	68325558	68325559	A	G	13	GENIC	homozygous	46196632
19	68326284	68326285	T	-	2	GENIC	homozygous	46301313
19	68326713	68326714	T	C	37	GENIC	homozygous	46301314
19	68326810	68326811	A	C	17	GENIC	homozygous	46301315
19	68327650	68327651	C	G	35	GENIC	homozygous	46301316