chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	145362202	145362202		G	20	GENIC	homozygous	132967632
4	145362359	145362360	T	C	19	GENIC	homozygous	119315406
4	145364439	145364440	T	C	15	GENIC	homozygous	112870819
4	145365227	145365228	T	C	20	GENIC	homozygous	119315407
4	145365339	145365340	T	C	24	GENIC	homozygous	119315408
4	145365611	145365612	A	G	29	GENIC	homozygous	119315409
4	145366289	145366290	G	A	21	GENIC	homozygous	119315410
4	145366477	145366478	C	T	28	GENIC	homozygous	119315411
4	145367615	145367616	C	T	20	GENIC	homozygous	119315412
4	145367873	145367875	GT		19	GENIC	homozygous	132967633
4	145367984	145367986	AC		14	GENIC	homozygous	132967634
4	145368068	145368068		T	22	GENIC	homozygous	132967635
4	145368069	145368070	T	C	24	GENIC	homozygous	119315413
4	145368083	145368084	G	A	25	GENIC	homozygous	119315414
4	145369708	145369709	T	C	18	GENIC	homozygous	112870823
4	145369904	145369905	A	C	31	GENIC	homozygous	112870824
4	145370077	145370078	C	T	30	GENIC	homozygous	119315415
4	145370443	145370444	T	A	21	GENIC	homozygous	112870825
4	145370957	145370958	A	T	25	GENIC	homozygous	112870826