chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	118854109	118854110	A	G	16	GENIC	homozygous	143150497
4	118854450	118854451	A	G	26	GENIC	homozygous	137193365
4	118854931	118854932	A	G	18	GENIC	homozygous	137193366
4	118855390	118855390		A	22	GENIC	homozygous	136911590
4	118857735	118857735		T	19	GENIC	homozygous	136911591
4	118857832	118857833	T	C	19	GENIC	homozygous	137193367
4	118858889	118858890	C	T	15	GENIC	homozygous	143150498
4	118864918	118864919	C	A	14	GENIC	heterozygous	137193371
4	118864920	118864921	A	G	14	GENIC	heterozygous	137193372
4	118865638	118865639	G	A	15	GENIC	homozygous	143150499
4	118865937	118865938	T	A	24	GENIC	homozygous	137193373
4	118867632	118867632		AAAC	15	GENIC	homozygous	136911593
4	118868186	118868187	T	C	16	GENIC	homozygous	137193374
4	118868413	118868414	C	T	25	GENIC	homozygous	143150500
4	118871790	118871791	A	G	3	GENIC	homozygous	143150501
4	118871788	118871789	A	G	3	GENIC	homozygous	141656036
4	118864909	118864910	C	T	15	GENIC	heterozygous	403991598
4	118864910	118864911	T	G	15	GENIC	heterozygous	403991599
4	118871978	118871979	T	A	17	GENIC	homozygous	154233935
4	118871978	118871979	T		17	GENIC	heterozygous	403588526
4	118876931	118876932	T	C	25	GENIC	homozygous	143150505
4	118882860	118882864	CTGT		21	GENIC	homozygous	143060742