chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	97458159	97458160	C	T	42	GENIC	homozygous	114434684
13	97458238	97458239	G	T	31	GENIC	homozygous	114434686
13	97458301	97458302	C	A	22	GENIC	homozygous	114434688
13	97458363	97458364	T	C	27	GENIC	homozygous	114434690
13	97458364	97458365	C	T	27	GENIC	homozygous	114434692
13	97462226	97462227	G	A	2	GENIC	homozygous	114693558
13	97462230	97462231	A	C	2	GENIC	homozygous	114693559
13	97462232	97462233	G	A	2	GENIC	homozygous	114693560
13	97556945	97556946	C	T	15	GENIC	homozygous	114434750
13	97559846	97559847	T	G	24	GENIC	homozygous	114434768
13	97559847	97559848	A	C	24	GENIC	homozygous	114583069
13	97559852	97559853	C	A	23	GENIC	homozygous	114583071
13	97575536	97575537	A	T	15	GENIC	homozygous	114434817
13	97580907	97580908	T	G	18	GENIC	homozygous	114693561
13	97580950	97580951	A	G	12	GENIC	homozygous	114583077
13	97583858	97583859	G	A	22	GENIC	homozygous	114583079
13	97589447	97589448	T	G	22	GENIC	homozygous	114434818
13	97589473	97589474	C	A	22	GENIC	homozygous	114434820
13	97589740	97589741	T	A	29	GENIC	homozygous	114434822
13	97608021	97608022	C	G	20	GENIC	homozygous	114583085
13	97608090	97608091	G	A	25	GENIC	possibly homozygous	114434832
13	97608403	97608404	A	G	5	GENIC	homozygous	114434838
13	97612511	97612512	A	G	21	GENIC	homozygous	114434859
13	97739019	97739020	T	C	30	GENIC	homozygous	114434861
13	97739020	97739021	C	T	31	GENIC	homozygous	114434863
13	97739345	97739346	T	C	25	GENIC	homozygous	114434869
13	97739346	97739347	C	T	25	GENIC	homozygous	114434871
13	97750533	97750534	C	G	21	GENIC	homozygous	114434948