chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	12075589	12075590	G	C	9	GENIC	homozygous	53790178
7	12076297	12076298	T	C	28	GENIC	homozygous	53790179
7	12076880	12076881	G	C	31	GENIC	homozygous	53790180
7	12076895	12076896	G	C	28	GENIC	homozygous	53790181
7	12076900	12076901	T	C	28	GENIC	homozygous	53790182
7	12077182	12077183	G	GT	25	GENIC	homozygous	56141855
7	12077379	12077380	C	G	30	GENIC	homozygous	53790183
7	12077693	12077694	C	T	26	GENIC	homozygous	56141858
7	12077868	12077869	T	C	23	GENIC	homozygous	53790184
7	12078691	12078692	G	A	31	GENIC	possibly homozygous	56141861
7	12078938	12078939	T	C	21	GENIC	homozygous	53790189
7	12081634	12081635	A	G	33	GENIC	possibly homozygous	53790193
7	12081869	12081870	A	G	30	GENIC	homozygous	53790194
7	12082819	12082820	A	G	33	GENIC	homozygous	56141864
7	12082905	12082906	T	G	40	GENIC	homozygous	53790195
7	12085137	12085138	T	G	20	GENIC	homozygous	56141867
7	12085798	12085800	TT	--	7	GENIC	possibly homozygous	54954754
7	12086033	12086068	CTCCTAGGCATCTGAGTTCTCAGCCATCAGTATGA	-----------------------------------	11	GENIC	homozygous	56141870
7	12085797	12085800	TTT	---	7	GENIC	heterozygous	55057491