chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	19402517	19402518	C	T	12	GENIC	homozygous	136649757
3	19407808	19407809	A	G	20	GENIC	homozygous	136649758
3	19409846	19409847	G		19	GENIC	homozygous	136551161
3	19410373	19410374	C	T	23	GENIC	homozygous	136649759
3	19413172	19413173	C		11	GENIC	homozygous	403058629
3	19413172	19413173	C	G	11	GENIC	heterozygous	403058630
3	19413168	19413169	C		11	GENIC	homozygous	403058627
3	19413168	19413169	C	G	11	GENIC	heterozygous	403058628
3	19416827	19416828	C		9	GENIC	possibly homozygous	136551162
3	19419167	19419167		TGAGTAGCTC	24	GENIC	homozygous	136551163
3	19422221	19422222	T	C	31	GENIC	homozygous	136649760
3	19422287	19422288	C	G	31	GENIC	homozygous	136649761
3	19422838	19422839	G	A	23	GENIC	homozygous	136649762
3	19424532	19424533	T	G	24	GENIC	homozygous	136649763
3	19424625	19424626	G	A	26	GENIC	possibly homozygous	136649764
3	19425817	19425818	G	A	25	GENIC	homozygous	136649765
3	19427246	19427249	GAT		14	GENIC	homozygous	136551164
3	19427370	19427371	G	A	8	GENIC	homozygous	154073380
3	19429275	19429276	A	G	15	GENIC	homozygous	136649766
3	19429353	19429354	C	G	26	GENIC	homozygous	136649767
3	19429719	19429720	T	C	21	GENIC	homozygous	136649768