chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	42711201	42711202	C	CA	43	GENIC	homozygous	48685117
14	42711204	42711205	C	-	41	GENIC	homozygous	48685118
14	42711383	42711384	A	G	50	GENIC	possibly homozygous	48685119
14	42711501	42711502	T	C	56	GENIC	homozygous	48685120
14	42712304	42712305	A	G	46	GENIC	homozygous	49178650
14	42712735	42712736	C	A	48	GENIC	possibly homozygous	48685122
14	42712839	42712840	T	C	46	GENIC	possibly homozygous	48685123
14	42713594	42713595	T	C	46	GENIC	homozygous	49178651
14	42713714	42713715	A	G	59	GENIC	homozygous	48685125
14	42713870	42713871	T	TA	29	GENIC	homozygous	49178652
14	42714470	42714471	A	G	59	GENIC	homozygous	48685127
14	42716112	42716115	GGG	---	37	GENIC	homozygous	49178653
14	42716157	42716158	C	T	45	GENIC	homozygous	49178654
14	42716180	42716181	T	C	43	GENIC	homozygous	48685131
14	42716826	42716827	A	-	26	GENIC	homozygous	49178655
14	42716882	42716883	C	A	42	GENIC	possibly homozygous	49178656
14	42716947	42716948	G	A	57	GENIC	homozygous	49178657
14	42717412	42717413	T	C	50	GENIC	possibly homozygous	48685133
14	42718587	42718588	T	A	56	GENIC	possibly homozygous	49178658