chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	180898138	180898139	A	G	13	GENIC	homozygous	110800742
2	180898172	180898173	G	A	15	GENIC	homozygous	110800743
2	180899134	180899135	G	A	21	GENIC	homozygous	110800745
2	180899312	180899313	A	G	26	GENIC	homozygous	110800746
2	180899631	180899632	T	C	25	GENIC	homozygous	110800747
2	180899755	180899756	C	T	31	GENIC	homozygous	110800748
2	180901332	180901333	T	C	27	GENIC	homozygous	110800749
2	180902408	180902409	A	G	14	GENIC	homozygous	110800750
2	180903152	180903153	A	T	18	GENIC	homozygous	110800751
2	180906629	180906630	A	C	21	GENIC	homozygous	110155214
2	180907151	180907152	T	C	25	GENIC	homozygous	110155215
2	180907719	180907720	T	A	19	GENIC	homozygous	110800752
2	180908056	180908057	T	A	22	GENIC	homozygous	110800753
2	180908111	180908112	G	A	16	GENIC	homozygous	110800754
2	180910701	180910702	A	C	21	GENIC	homozygous	110155217
2	180911479	180911480	T	C	42	GENIC	homozygous	110155218
2	180911824	180911825	C	G	36	GENIC	homozygous	110800755
2	180911828	180911829	G	A	34	GENIC	homozygous	110800756