chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	137712276	137712277	T	C	30	GENIC	homozygous	114997559
6	137712441	137712442	T	G	32	GENIC	homozygous	114997560
6	137713745	137713746	G	A	35	GENIC	homozygous	114997561
6	137714202	137714203	A	G	24	GENIC	homozygous	114997563
6	137714400	137714401	C	T	32	GENIC	homozygous	114997564
6	137716129	137716130	A	G	45	GENIC	homozygous	114997565
6	137718815	137718816	G	A	38	GENIC	homozygous	114997566
6	137719199	137719200	A	G	37	GENIC	homozygous	114997567
6	137719685	137719686	T	C	33	GENIC	homozygous	114997568
6	137721764	137721765	C	T	37	GENIC	possibly homozygous	114997569
6	137721910	137721911	T	C	35	GENIC	homozygous	114997570
6	137722235	137722236	A	G	48	GENIC	homozygous	114997571
6	137722344	137722345	C	T	40	GENIC	homozygous	114997572
6	137725090	137725091	C	T	45	GENIC	homozygous	114997573
6	137726909	137726910	C	T	53	GENIC	possibly homozygous	114997574
6	137727023	137727024	T	C	22	GENIC	possibly homozygous	114997575
6	137727236	137727237	C	T	50	GENIC	homozygous	114997576
6	137727947	137727948	C	G	26	GENIC	homozygous	114997577
6	137728086	137728087	T	C	48	GENIC	homozygous	114997578
6	137730206	137730207	T	C	36	GENIC	homozygous	114997579
6	137730875	137730876	A	C	31	GENIC	homozygous	114997580