chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	41711255	41711283	GTGTGTGTGTGTGTGTGTGTGTGTGTGA		12	GENIC	heterozygous	132433177
19	41711358	41711359	T	A	15	GENIC	heterozygous	134465786
19	41711589	41711590	A	G	57	GENIC	homozygous	109702453
19	41712740	41712741	T	C	53	GENIC	homozygous	109702455
19	41713883	41713884	A	G	60	GENIC	homozygous	109702459
19	41714308	41714309	T	C	57	GENIC	homozygous	109702461
19	41715849	41715850	T	C	56	GENIC	homozygous	109702463
19	41719537	41719538	G	A	25	GENIC	homozygous	132239405
19	41719556	41719557	C	T	32	GENIC	homozygous	132239406
19	41720002	41720003	T	C	73	GENIC	homozygous	109702467
19	41721497	41721497		G	27	GENIC	possibly homozygous	129609423
19	41716191	41716191		G	60	GENIC	homozygous	129609418
19	41719719	41719720	G		67	GENIC	homozygous	129609421
19	41719724	41719725	A		67	GENIC	homozygous	129609422
19	41718532	41718533	A	G	57	GENIC	homozygous	109817195
19	41719807	41719808	G	A	65	GENIC	possibly homozygous	109817197
19	41723502	41723506	TGTG		19	GENIC	heterozygous	129609426
19	41723519	41723520	G	A	20	GENIC	heterozygous	132239407
19	41723557	41723558	A	G	24	GENIC	heterozygous	132367271
19	41723565	41723566	A	G	25	GENIC	heterozygous	132239408
19	41723949	41723950	A	T	29	GENIC	possibly homozygous	109817199
19	41723861	41723862	A	C	7	GENIC	homozygous	110035902
19	41723524	41723526	TG		10	GENIC	heterozygous	132235390