chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	11305711	11305712	T	C	26	GENIC	homozygous	136971001
4	11306694	11306695	A	C	22	GENIC	homozygous	136971002
4	11307330	11307331	T	C	30	GENIC	homozygous	136971003
4	11307539	11307540	G	A	25	GENIC	homozygous	136971004
4	11307717	11307718	C	G	21	GENIC	homozygous	136971005
4	11307990	11307991	A	G	22	GENIC	homozygous	136971006
4	11308286	11308287	G	A	26	GENIC	homozygous	136971007
4	11310106	11310107	G	T	26	GENIC	homozygous	136971008
4	11310585	11310586	T		6	GENIC	heterozygous	147397770
4	11311004	11311005	T	C	31	GENIC	homozygous	136971009
4	11311560	11311561	T	C	21	GENIC	homozygous	136971010
4	11311626	11311627	T	G	33	GENIC	possibly homozygous	136971011
4	11310604	11310605	T	C	9	GENIC	heterozygous	149129297
4	11308579	11308581	TG		27	GENIC	homozygous	136866704
4	11311421	11311422	T		12	GENIC	possibly homozygous	136866705
4	11311445	11311445		T	12	GENIC	homozygous	136866706
4	11310571	11310572	T	C	5	GENIC	heterozygous	140877699
4	11310572	11310573	C	T	5	GENIC	heterozygous	140877700
4	11310579	11310580	T	C	6	GENIC	heterozygous	140877701
4	11310599	11310600	T	C	9	GENIC	heterozygous	149129296
4	11310595	11310596	T		8	GENIC	heterozygous	403955349
4	11310595	11310596	T	C	8	GENIC	heterozygous	403955348