chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	107767411	107767412	A	C	45	INTERGENIC	heterozygous	48891146
14	107767422	107767423	A	C	43	INTERGENIC	heterozygous	49188102
14	107767433	107767434	A	C	41	INTERGENIC	heterozygous	48891148
14	107767435	107767436	C	T	41	INTERGENIC	heterozygous	48891150
14	107767444	107767445	C	A	33	INTERGENIC	heterozygous	48891152
14	107767446	107767447	C	T	31	INTERGENIC	heterozygous	48891154
14	107767501	107767502	C	T	22	INTERGENIC	heterozygous	49188106
14	107767510	107767511	A	C	20	INTERGENIC	heterozygous	49188108
14	107767512	107767513	T	C	21	INTERGENIC	heterozygous	49188110
14	107767532	107767533	C	A	20	INTERGENIC	heterozygous	49188112
14	107767556	107767557	T	C	18	INTERGENIC	heterozygous	49188114
14	107767565	107767566	A	C	17	INTERGENIC	heterozygous	49188116
14	107767578	107767579	T	C	15	INTERGENIC	heterozygous	49188118
14	107767611	107767612	T	C	22	INTERGENIC	heterozygous	49188120
14	107767912	107767913	T	C	38	INTERGENIC	homozygous	48891156
14	107769265	107769271	TCTCTC	------	9	INTERGENIC	heterozygous	48891160
14	107769267	107769271	TCTC	----	9	INTERGENIC	heterozygous	48891162
14	107771145	107771146	A	AT	25	INTERGENIC	homozygous	49188121
14	107772134	107772135	C	CA	27	INTERGENIC	homozygous	48891170
14	107772869	107772871	CG	--	22	INTERGENIC	heterozygous	48891173
14	107775629	107775630	T	TA	20	INTERGENIC	homozygous	49188123
14	107776856	107776857	T	C	35	INTERGENIC	homozygous	48891188
14	107777552	107777553	T	C	26	INTERGENIC	homozygous	48891190