chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	42711201	42711202	C	-	26	GENIC	homozygous	49307377
14	42711204	42711205	C	CA	27	GENIC	homozygous	49307378
14	42711383	42711384	A	G	29	GENIC	homozygous	48685119
14	42711501	42711502	T	C	26	GENIC	homozygous	48685120
14	42711602	42711603	C	T	31	GENIC	homozygous	48685121
14	42712735	42712736	C	A	31	GENIC	homozygous	48685122
14	42712839	42712840	T	C	27	GENIC	homozygous	48685123
14	42713209	42713210	G	T	17	GENIC	homozygous	48685124
14	42713714	42713715	A	G	24	GENIC	homozygous	48685125
14	42713859	42713860	G	T	21	GENIC	homozygous	48685126
14	42714470	42714471	A	G	14	GENIC	homozygous	48685127
14	42715478	42715479	C	G	27	GENIC	homozygous	48685128
14	42715569	42715570	C	CTGTTGTTGTTGTTGT	9	GENIC	heterozygous	49307379
14	42715569	42715570	C	CTGTTGTTGTTGTTGTTGT	9	GENIC	possibly homozygous	49307380
14	42715811	42715812	G	A	26	GENIC	homozygous	48685130
14	42716180	42716181	T	C	22	GENIC	homozygous	48685131
14	42717206	42717207	C	T	33	GENIC	homozygous	48685132
14	42717412	42717413	T	C	30	GENIC	homozygous	48685133