chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	73247361	73247362	G	T	19	GENIC	homozygous	136152318
2	73247665	73247666	C	T	47	GENIC	homozygous	136152319
2	73248051	73248052	G	T	26	GENIC	homozygous	136152320
2	73248299	73248300	G	A	43	GENIC	homozygous	136152321
2	73248372	73248373	T	G	43	GENIC	homozygous	143842646
2	73248456	73248457	G	A	22	GENIC	homozygous	136152322
2	73248479	73248480	T	C	12	GENIC	homozygous	136152323
2	73248598	73248599	C	A	36	GENIC	homozygous	136152324
2	73248750	73248751	G	A	37	GENIC	homozygous	136152325
2	73248913	73248914	C	G	36	GENIC	homozygous	136152326
2	73249072	73249073	T	C	43	GENIC	homozygous	136152327
2	73249171	73249172	A	T	46	GENIC	homozygous	143842647
2	73249390	73249391	T	C	34	GENIC	homozygous	136152328
2	73249449	73249450	C	G	30	GENIC	homozygous	136152329
2	73249515	73249516	C	T	34	GENIC	possibly homozygous	143842648
2	73249632	73249633	G	T	44	GENIC	homozygous	136152330
2	73249640	73249641	A	G	44	GENIC	homozygous	136152331
2	73249167	73249167		C	45	GENIC	homozygous	143818513
2	73248537	73248538	C		18	GENIC	homozygous	135916822