chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	46351323	46351324	A		19	GENIC	homozygous	143855486
3	46353203	46353204	A	T	8	GENIC	heterozygous	154105653
3	46353203	46353204	A		8	GENIC	homozygous	403809478
3	46353340	46353341	G		6	GENIC	homozygous	403809479
3	46353340	46353341	G	A	6	GENIC	heterozygous	403809480
3	46353612	46353613	C		6	GENIC	homozygous	403809481
3	46353612	46353613	C	T	6	GENIC	heterozygous	403809482
3	46354647	46354647		A	22	GENIC	homozygous	143855488
3	46357309	46357310	G	T	20	GENIC	homozygous	143883756
3	46353342	46353343	G		6	GENIC	homozygous	403984463
3	46353342	46353343	G	A	6	GENIC	heterozygous	403984464
3	46353767	46353768	A	G	16	GENIC	homozygous	143883752
3	46354114	46354115	C	G	24	GENIC	homozygous	143883753
3	46355659	46355660	C	G	21	GENIC	homozygous	143883754
3	46356682	46356683	G	A	18	GENIC	homozygous	143883755
3	46355800	46355804	GCTG		14	GENIC	homozygous	140985054
3	46357504	46357505	C	T	22	GENIC	homozygous	143883757
3	46358297	46358298	A		26	GENIC	homozygous	143855489
3	46359410	46359410		CCT	32	GENIC	homozygous	143855490
3	46359528	46359528		T	19	GENIC	homozygous	143855491
3	46360296	46360300	TCCC		8	GENIC	homozygous	140985055
3	46361625	46361626	A	G	25	GENIC	homozygous	143883758
3	46362411	46362412	C	T	21	GENIC	homozygous	143883759
3	46363919	46363920	C		19	GENIC	homozygous	143855492
3	46365013	46365013		T	16	GENIC	homozygous	143855493
3	46366242	46366243	A	C	23	GENIC	homozygous	143883760
3	46368065	46368066	A		5	GENIC	homozygous	403809485
3	46368065	46368066	A	C	5	GENIC	heterozygous	403809486
3	46368371	46368372	C	T	22	GENIC	homozygous	143883761