chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	36404331	36404332	C	A	28	GENIC	homozygous	55229158
6	36404368	36404369	T	C	37	GENIC	homozygous	55229160
6	36404780	36404781	G	A	33	GENIC	homozygous	55229162
6	36405000	36405001	A	AT	35	GENIC	homozygous	55229164
6	36405571	36405572	G	A	29	GENIC	homozygous	55229166
6	36405891	36405892	G	A	27	GENIC	homozygous	56248185
6	36406008	36406009	C	T	22	GENIC	homozygous	55229168
6	36406187	36406188	T	TG	29	GENIC	homozygous	55229170
6	36406645	36406646	T	C	21	GENIC	homozygous	55229174
6	36406881	36406882	G	GT	18	GENIC	homozygous	56248186
6	36407453	36407454	C	T	30	GENIC	homozygous	55229180
6	36407768	36407769	T	G	30	GENIC	homozygous	55229186
6	36408277	36408278	A	G	30	GENIC	homozygous	55229188
6	36408295	36408296	C	T	31	GENIC	homozygous	55229190
6	36408704	36408705	G	-	19	GENIC	homozygous	56248187
6	36408958	36408959	A	G	32	GENIC	homozygous	56248188
6	36409217	36409222	TACTG	-----	23	GENIC	homozygous	56248189
6	36409253	36409254	A	G	27	GENIC	homozygous	56248190
6	36409264	36409265	C	-	26	GENIC	homozygous	56248191
6	36409291	36409292	T	-	20	GENIC	homozygous	56248192
6	36409324	36409325	T	C	31	GENIC	homozygous	56248193
6	36409381	36409382	A	G	27	GENIC	homozygous	56248194
6	36410107	36410108	A	G	18	GENIC	homozygous	55229196
6	36411466	36411467	C	CAA	4	GENIC	homozygous	55493877
6	36412221	36412222	T	C	33	GENIC	homozygous	55229203
6	36415367	36415368	G	T	26	GENIC	homozygous	55229205
6	36415806	36415812	ATATAT	------	20	GENIC	heterozygous	55229211
6	36415808	36415812	ATAT	----	20	GENIC	possibly homozygous	55699624
6	36416578	36416579	A	G	36	GENIC	homozygous	55229213