chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	100663501	100663502	A	G	37	GENIC	homozygous	50266474
13	100664230	100664231	A	T	35	GENIC	homozygous	50447674
13	100664281	100664284	TTT	---	22	GENIC	homozygous	50447676
13	100665036	100665037	T	C	44	GENIC	homozygous	50447678
13	100666607	100666608	G	A	26	GENIC	homozygous	50266479
13	100667409	100667436	TGATCCTCCCATCTCAAATTAGCTAAG	---------------------------	24	GENIC	homozygous	50533667
13	100667964	100667965	T	G	32	GENIC	homozygous	50266480
13	100668057	100668058	T	C	27	GENIC	homozygous	50266481
13	100668111	100668112	T	-	27	GENIC	homozygous	50266482
13	100669346	100669347	T	G	23	GENIC	homozygous	50447680
13	100671249	100671250	G	A	29	GENIC	homozygous	50447682
13	100671308	100671309	A	-	24	GENIC	homozygous	50266486
13	100672745	100672746	T	TAA	18	GENIC	homozygous	50266488
13	100673190	100673191	T	-	23	GENIC	homozygous	50447684
13	100673528	100673529	C	T	32	GENIC	homozygous	50447686
13	100674467	100674468	T	G	28	GENIC	homozygous	50266490
13	100674847	100674848	T	C	38	GENIC	homozygous	50266491
13	100676295	100676296	C	T	37	GENIC	homozygous	50447688
13	100678158	100678159	G	-	14	GENIC	homozygous	50266493
13	100678272	100678273	T	TA	4	GENIC	homozygous	50201858
13	100678727	100678728	C	T	6	GENIC	homozygous	50447690