chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	109714477	109714478	C	T	28	GENIC	homozygous	114701430
13	109714746	109714747	T	C	25	GENIC	homozygous	114701432
13	109715880	109715881	A	G	22	GENIC	homozygous	114701434
13	109716498	109716499	C	T	29	GENIC	homozygous	114701436
13	109716773	109716774	C	G	29	GENIC	homozygous	114701438
13	109718665	109718666	A	C	33	GENIC	homozygous	114701440
13	109719342	109719343	T	C	25	GENIC	homozygous	114701442
13	109720457	109720458	A	G	29	GENIC	homozygous	114443464
13	109721234	109721235	T	C	33	GENIC	homozygous	114443466
13	109721261	109721262	A	G	36	GENIC	homozygous	114701444
13	109721497	109721498	C	T	32	GENIC	homozygous	114701446
13	109725114	109725115	T	C	21	GENIC	homozygous	114443476
13	109725273	109725274	T	G	22	GENIC	homozygous	114701448
13	109725443	109725444	C	T	24	GENIC	homozygous	114701450
13	109726218	109726219	A	T	27	GENIC	homozygous	114443482