chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	148875730	148875731	C	T	18	GENIC	homozygous	110050329
2	148876657	148876658	A	G	23	GENIC	homozygous	110050332
2	148876659	148876660	G	A	23	GENIC	homozygous	110050333
2	148876901	148876902	T	G	31	GENIC	homozygous	110050335
2	148877800	148877801	C	G	34	GENIC	homozygous	110050336
2	148877883	148877884	T	C	30	GENIC	homozygous	110050337
2	148878525	148878526	T	C	17	GENIC	homozygous	110050338
2	148879948	148879949	C	G	16	GENIC	homozygous	110050339
2	148880009	148880010	C	T	9	GENIC	homozygous	110050340
2	148883146	148883147	G	A	37	GENIC	homozygous	110050341
2	148883729	148883730	G	A	19	GENIC	homozygous	110050342
2	148884321	148884322	G	A	16	GENIC	homozygous	110050343
2	148886666	148886667	T	G	12	GENIC	homozygous	110050344
2	148887242	148887243	T	C	17	GENIC	homozygous	110050346
2	148888053	148888054	A	G	16	GENIC	homozygous	110050347
2	148888370	148888371	A	G	16	GENIC	homozygous	110050349
2	148889016	148889017	C	T	17	GENIC	homozygous	110050352
2	148889206	148889207	G	A	16	GENIC	homozygous	110050353
2	148889494	148889495	G	T	9	GENIC	homozygous	110050354
2	148889501	148889502	T	C	9	GENIC	homozygous	110050355
2	148889532	148889533	G	C	10	GENIC	homozygous	110050356
2	148890085	148890086	A	G	20	GENIC	homozygous	110050357
2	148890319	148890320	T	A	22	GENIC	homozygous	110050358
2	148890557	148890558	G	T	22	GENIC	homozygous	110050359
2	148890813	148890814	T	C	28	GENIC	possibly homozygous	110050360