chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	49338436	49338437	C	T	16	GENIC	homozygous	115152158
13	49382317	49382318	C		13	GENIC	heterozygous	129052227
13	49454115	49454116	T		22	GENIC	homozygous	129052228
13	49454123	49454124	G	C	24	GENIC	homozygous	114337998
13	49454125	49454126	T	C	23	GENIC	homozygous	114338000
13	49454132	49454133	C	A	20	GENIC	homozygous	114338002
13	49454134	49454135	G		20	GENIC	homozygous	129052229
13	49454139	49454140	T	C	19	GENIC	homozygous	114338004
13	49454178	49454179	C		18	GENIC	homozygous	129052230
13	49454193	49454194	T		20	GENIC	homozygous	129052231
13	49454197	49454198	A	C	22	GENIC	homozygous	114338006
13	49454211	49454212	T		20	GENIC	homozygous	129052232
13	49454217	49454218	T		20	GENIC	possibly homozygous	129052233
13	49456910	49456910		A	14	GENIC	heterozygous	131126296
13	49473157	49473158	G		16	GENIC	heterozygous	131501757
13	49473193	49473194	T	C	17	GENIC	heterozygous	118450435
13	49480913	49480914	T	C	28	GENIC	heterozygous	133684723
13	49480530	49480531	G	A	18	GENIC	heterozygous	129109151
13	49480540	49480541	A	T	18	GENIC	heterozygous	129109153
13	49481053	49481054	C	T	27	GENIC	heterozygous	129109158
13	49482204	49482205	T	C	14	GENIC	heterozygous	130587044