chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	46351482	46351483	T	C	58	GENIC	homozygous	146376139
3	46353203	46353204	A	T	16	GENIC	possibly homozygous	154105653
3	46353203	46353204	A		16	GENIC	heterozygous	403809478
3	46353340	46353341	G		10	GENIC	heterozygous	403809479
3	46353340	46353341	G	A	10	GENIC	heterozygous	403809480
3	46353612	46353613	C		12	GENIC	heterozygous	403809481
3	46353612	46353613	C	T	12	GENIC	heterozygous	403809482
3	46355800	46355804	GCTG		39	GENIC	homozygous	140985054
3	46357309	46357310	G	T	48	GENIC	homozygous	143883756
3	46354114	46354115	C	G	42	GENIC	homozygous	143883753
3	46355659	46355660	C	G	54	GENIC	homozygous	143883754
3	46356682	46356683	G	A	55	GENIC	homozygous	143883755
3	46355147	46355148	A		38	GENIC	homozygous	146367978
3	46358297	46358298	A		39	GENIC	homozygous	143855489
3	46358730	46358731	G	T	45	GENIC	possibly homozygous	146376140
3	46360296	46360300	TCCC		25	GENIC	homozygous	140985055
3	46363919	46363920	C		50	GENIC	possibly homozygous	143855492
3	46365013	46365013		T	39	GENIC	homozygous	143855493
3	46366242	46366243	A	C	43	GENIC	homozygous	143883760
3	46366823	46366824	C	G	44	GENIC	homozygous	146376141
3	46367757	46367758	A	G	29	GENIC	heterozygous	403809483
3	46367757	46367758	A		29	GENIC	homozygous	403809484
3	46368065	46368066	A		28	GENIC	heterozygous	403809485
3	46368371	46368372	C	T	41	GENIC	homozygous	143883761
3	46367755	46367756	A		29	GENIC	homozygous	403062571
3	46367755	46367756	A	G	29	GENIC	heterozygous	403062572
3	46368065	46368066	A	C	28	GENIC	heterozygous	403809486