chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	106630469	106630470	A	AT	25	GENIC	homozygous	49874241
13	106630574	106630601	TGCGCTTGCTAGGCAAGCGCTCTACCA	---------------------------	28	GENIC	homozygous	51204481
13	106630790	106630791	C	A	26	GENIC	homozygous	51204482
13	106631094	106631095	C	A	29	GENIC	homozygous	51204483
13	106631137	106631138	G	A	24	GENIC	homozygous	51204484
13	106632934	106632935	C	-	21	GENIC	homozygous	49874242
13	106633614	106633617	TTA	---	10	GENIC	homozygous	49874243
13	106633641	106633642	T	A	11	GENIC	homozygous	49977949
13	106636540	106636541	T	C	16	GENIC	homozygous	51204485
13	106636543	106636544	T	C	16	GENIC	homozygous	51204486
13	106636545	106636546	C	A	16	GENIC	homozygous	51204487
13	106636548	106636549	A	G	16	GENIC	homozygous	51204488
13	106636590	106636591	T	A	10	GENIC	homozygous	49977954
13	106636632	106636633	T	A	13	GENIC	homozygous	50272426
13	106636641	106636642	A	C	16	GENIC	homozygous	50272427
13	106637527	106637528	G	A	8	GENIC	homozygous	51204489
13	106637596	106637597	G	A	2	GENIC	homozygous	51204490
13	106637713	106637714	G	GA	11	GENIC	homozygous	51204491
13	106639013	106639014	A	-	11	GENIC	homozygous	49874244
13	106639807	106639817	AGAGGCGCAG	----------	7	GENIC	homozygous	51204492
13	106644004	106644034	GGCCACCCGAAGCTCTTCTATCAATAAAAG	------------------------------	14	GENIC	homozygous	50961043
13	106644125	106644126	T	C	12	GENIC	homozygous	49977971
13	106645040	106645041	A	-	6	GENIC	heterozygous	50554376
13	106645376	106645377	G	GA	18	GENIC	possibly homozygous	49977975
13	106645754	106645756	CA	--	35	GENIC	homozygous	49977977
13	106646417	106646418	C	G	17	GENIC	homozygous	50150962
13	106646871	106646872	G	A	32	GENIC	homozygous	51204493
13	106647619	106647620	G	A	17	GENIC	homozygous	49977989
13	106647634	106647635	G	A	13	GENIC	homozygous	51204494
13	106647640	106647641	G	GGAAGAGGAAGAA	13	GENIC	homozygous	51204495