chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	47012175	47012176	C	T	41	GENIC	homozygous	115343010
12	47013955	47013956	C	T	10	GENIC	homozygous	115343012
12	47014655	47014656	A	G	32	GENIC	possibly homozygous	115343014
12	47015629	47015630	T	C	32	GENIC	homozygous	115343016
12	47015899	47015900	C	T	12	GENIC	homozygous	118272549
12	47016310	47016311	C	T	30	GENIC	homozygous	115343018
12	47018601	47018602	A	T	14	GENIC	homozygous	115343020
12	47018607	47018608	A	T	14	GENIC	homozygous	115343022
12	47018940	47018941	A	G	18	GENIC	homozygous	115343024
12	47019959	47019960	C	T	27	GENIC	possibly homozygous	115343026
12	47021025	47021026	G	A	20	GENIC	homozygous	115343028
12	47021238	47021239	G	A	8	GENIC	homozygous	118272550