chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	187114527	187114528	A	G	48	GENIC	homozygous	110166929
2	187114784	187114785	T	C	36	GENIC	homozygous	110166930
2	187114917	187114918	A	G	40	GENIC	homozygous	110166931
2	187115561	187115562	A	G	28	GENIC	homozygous	110166932
2	187116861	187116862	A	G	62	GENIC	homozygous	110166933
2	187118980	187118981	G	A	45	GENIC	homozygous	110166934
2	187119480	187119481	G	A	38	GENIC	homozygous	110166935
2	187120335	187120336	G	A	38	GENIC	homozygous	110166936
2	187121209	187121210	A	G	44	GENIC	homozygous	110166937
2	187121900	187121901	A	G	43	GENIC	homozygous	110166938
2	187123110	187123111	C	G	40	GENIC	homozygous	110166939
2	187123947	187123948	C	T	43	GENIC	homozygous	110166940
2	187124170	187124171	G	A	40	GENIC	homozygous	110166941
2	187124695	187124696	G	A	50	GENIC	homozygous	110166942
2	187125163	187125164	C	T	49	GENIC	homozygous	110166943
2	187126341	187126342	G	A	45	GENIC	homozygous	110166944
2	187127537	187127538	G	A	49	GENIC	homozygous	110166945
2	187129159	187129160	C	T	22	GENIC	homozygous	110166946
2	187129762	187129763	C	T	42	GENIC	homozygous	110166947
2	187130331	187130332	G	A	41	GENIC	homozygous	110166948
2	187130911	187130912	A	G	45	GENIC	homozygous	110166949
2	187134101	187134102	C	G	38	GENIC	homozygous	110166950
2	187121113	187121114	G		29	GENIC	possibly homozygous	127716660