chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	68314070	68314071	C	CA	27	GENIC	homozygous	46301299
19	68314388	68314389	A	G	45	GENIC	homozygous	46301300
19	68314605	68314606	G	A	49	GENIC	homozygous	46196617
19	68314644	68314645	T	C	46	GENIC	homozygous	46196618
19	68315539	68315540	G	T	31	GENIC	homozygous	46196620
19	68316209	68316210	G	A	42	GENIC	homozygous	46301301
19	68317652	68317653	G	T	24	GENIC	homozygous	46301302
19	68317659	68317660	A	T	24	GENIC	homozygous	46301303
19	68318399	68318400	C	T	34	GENIC	homozygous	46196622
19	68318483	68318484	C	T	35	GENIC	homozygous	46301304
19	68318576	68318577	A	G	37	GENIC	homozygous	46196623
19	68319337	68319338	C	T	44	GENIC	homozygous	46196625
19	68319767	68319768	G	GGACACCCTCCCTGCT	12	GENIC	homozygous	46196627
19	68320091	68320092	T	C	29	GENIC	homozygous	46301305
19	68322765	68322779	TGAGATAACTTTTT	--------------	10	GENIC	homozygous	46301306
19	68322948	68322949	A	T	30	GENIC	homozygous	46301307
19	68323545	68323546	T	C	43	GENIC	homozygous	46301308
19	68323764	68323765	T	C	51	GENIC	homozygous	46301309
19	68324419	68324420	T	A	30	GENIC	possibly homozygous	46301310
19	68325046	68325047	T	TG	19	GENIC	homozygous	46301311
19	68325050	68325051	G	GA	16	GENIC	heterozygous	46196629
19	68325064	68325067	AAA	---	15	GENIC	homozygous	46301312
19	68325558	68325559	A	G	22	GENIC	homozygous	46196632
19	68326284	68326285	T	-	20	GENIC	homozygous	46301313
19	68326713	68326714	T	C	27	GENIC	homozygous	46301314
19	68326810	68326811	A	C	13	GENIC	homozygous	46301315
19	68327650	68327651	C	G	28	GENIC	homozygous	46301316
19	68321149	68321150	C	G	32	GENIC	possibly homozygous	46311821