chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	34850175	34850176	T	C	19	GENIC	homozygous	136072528
2	34851080	34851081	C	G	20	GENIC	homozygous	140976273
2	34853613	34853614	C	T	14	GENIC	homozygous	140976274
2	34854061	34854062	T	C	18	GENIC	homozygous	136072529
2	34855468	34855469	A	G	29	GENIC	homozygous	136072530
2	34858379	34858380	A	G	15	GENIC	homozygous	136072533
2	34858906	34858907	A	G	24	GENIC	homozygous	136072534
2	34860347	34860347		GTGTTTCA	21	GENIC	homozygous	135898768
2	34853156	34853157	T		26	GENIC	homozygous	140968026
2	34864313	34864314	T	C	22	GENIC	homozygous	136072542
2	34865832	34865833	A	T	18	GENIC	homozygous	136072544
2	34866845	34866846	A	G	18	GENIC	homozygous	136072545
2	34870388	34870389	T	G	20	GENIC	homozygous	140976275
2	34874817	34874818	A	T	17	GENIC	homozygous	140976276
2	34879879	34879880	T	C	20	GENIC	homozygous	136072557
2	34880463	34880464	C	T	14	GENIC	homozygous	140976277
2	34882489	34882490	A	G	23	GENIC	homozygous	136072562
2	34865696	34865699	TAT		5	GENIC	homozygous	135898772
2	34866294	34866295	A		19	GENIC	homozygous	135898773
2	34873019	34873020	A		15	GENIC	possibly homozygous	135898774
2	34879653	34879653		TT	14	GENIC	homozygous	140968028