chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	149148705	149148706	A	G	34	GENIC	homozygous	112036026
3	149154341	149154342	T	A	30	GENIC	homozygous	119744236
3	149154772	149154773	G	T	34	GENIC	homozygous	119744237
3	149156470	149156471	G	A	37	GENIC	homozygous	119744238
3	149157376	149157377	C	A	34	GENIC	homozygous	112036070
3	149157684	149157685	C	T	25	GENIC	homozygous	119744239
3	149158986	149158987	T	C	31	GENIC	homozygous	112365791
3	149159025	149159026	A	G	43	GENIC	homozygous	112365792
3	149159133	149159134	C	T	25	GENIC	homozygous	119744240
3	149159293	149159294	C	T	7	GENIC	homozygous	119744241
3	149160444	149160445	C	T	26	GENIC	homozygous	119744242
3	149160688	149160689	T	C	32	GENIC	homozygous	112036090
3	149161121	149161122	A	C	31	GENIC	homozygous	119744243
3	149161266	149161267	G	T	37	GENIC	homozygous	112036094
3	149161758	149161759	G	A	24	GENIC	homozygous	112036098
3	149163556	149163557	G	A	29	GENIC	homozygous	119744244
3	149163705	149163706	A	G	28	GENIC	homozygous	112036106
3	149164141	149164142	A	C	37	GENIC	homozygous	119744245
3	149164513	149164514	C	T	36	GENIC	homozygous	119744246
3	149164763	149164764	G	A	31	GENIC	homozygous	119744247
3	149167409	149167410	G	T	30	GENIC	homozygous	112036134
3	149167896	149167897	T	G	32	GENIC	homozygous	112036140
3	149168546	149168547	G	A	25	GENIC	homozygous	119744248