chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	45526812	45526813	T	G	28	GENIC	homozygous	116877159
10	45527043	45527044	G	T	16	GENIC	possibly homozygous	116877161
10	45527168	45527169	T	C	16	GENIC	homozygous	116877163
10	45527293	45527294	A	G	22	GENIC	homozygous	116877165
10	45527500	45527501	C	T	24	GENIC	homozygous	116877167
10	45527755	45527756	C	G	20	GENIC	homozygous	116877169
10	45527899	45527900	A	G	31	GENIC	homozygous	116583895
10	45528271	45528272	T	C	22	GENIC	homozygous	116877171
10	45528412	45528413	C	T	25	GENIC	homozygous	116877173
10	45528865	45528866	C		27	GENIC	homozygous	131092431
10	45529716	45529717	C	T	25	GENIC	homozygous	116877175
10	45529792	45529796	TAGC		28	GENIC	homozygous	131092432
10	45529901	45529902	C	T	34	GENIC	homozygous	116877177
10	45530246	45530247	G	A	26	GENIC	homozygous	116877179
10	45530751	45530752	T	C	26	GENIC	homozygous	116877181
10	45530854	45530855	T	C	18	GENIC	homozygous	116877183
10	45532413	45532414	C	G	32	GENIC	homozygous	116877185
10	45533199	45533200	C	T	26	GENIC	homozygous	116877187
10	45533751	45533752	T	C	9	GENIC	homozygous	116977584
10	45534063	45534064	G	A	31	GENIC	homozygous	116877189
10	45534868	45534869	T	C	25	GENIC	homozygous	116877191
10	45533750	45533751	T		9	GENIC	homozygous	130392259