chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	67341834	67341835	G	T	19	GENIC	homozygous	58861011
2	67341977	67341979	TT	--	2	GENIC	homozygous	58861012
2	67341985	67341986	T	G	2	GENIC	homozygous	60444660
2	67341997	67341998	C	G	3	GENIC	homozygous	58861013
2	67342076	67342077	G	A	21	GENIC	homozygous	58861014
2	67342187	67342188	G	A	15	GENIC	homozygous	58861015
2	67342627	67342628	T	C	6	GENIC	homozygous	58861016
2	67342706	67342708	AA	--	2	GENIC	homozygous	58861017
2	67342908	67342909	T	C	12	GENIC	homozygous	58861018
2	67342957	67342958	G	A	10	GENIC	homozygous	58861019
2	67343586	67343587	G	GT	21	GENIC	possibly homozygous	58861020
2	67343655	67343656	G	A	14	GENIC	homozygous	58861021
2	67344124	67344125	T	C	12	GENIC	homozygous	58861022
2	67344262	67344263	G	A	19	GENIC	homozygous	58861023
2	67344467	67344468	T	C	13	GENIC	homozygous	58861024
2	67344821	67344822	C	T	3	GENIC	homozygous	58861025
2	67345324	67345325	T	G	6	GENIC	homozygous	58861027
2	67345488	67345489	T	A	20	GENIC	possibly homozygous	58861028
2	67345635	67345636	T	G	10	GENIC	homozygous	58861029
2	67345643	67345644	G	A	8	GENIC	homozygous	58861030
2	67345904	67345905	T	C	28	GENIC	possibly homozygous	58861031
2	67346520	67346521	A	G	9	GENIC	homozygous	58861032
2	67349524	67349525	T	C	15	GENIC	possibly homozygous	58861042
2	67349567	67349568	A	G	11	GENIC	homozygous	58861043
2	67350147	67350148	C	T	16	GENIC	possibly homozygous	58861045