chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	107496959	107496960	T	G	30	GENIC	heterozygous	49874482
13	107501639	107501641	TG	--	33	GENIC	heterozygous	49874483
13	107501656	107501657	G	A	36	GENIC	heterozygous	49980617
13	107501660	107501662	AG	--	31	GENIC	heterozygous	49874484
13	107509953	107509954	C	-	19	GENIC	homozygous	49874487
13	107509962	107509963	A	T	17	GENIC	homozygous	49874488
13	107510030	107510031	C	-	10	GENIC	homozygous	49874489
13	107510045	107510046	A	-	9	GENIC	homozygous	49874490
13	107510055	107510056	G	T	11	GENIC	homozygous	49874491
13	107510074	107510075	A	G	13	GENIC	homozygous	49874492
13	107510080	107510081	T	TGGGG	13	GENIC	homozygous	49874493
13	107511680	107511681	C	CTTA	1	GENIC	homozygous	49874494
13	107518254	107518255	G	T	11	GENIC	possibly homozygous	49874496
13	107525433	107525437	GATA	----	9	GENIC	homozygous	49874497
13	107545937	107545939	TA	--	8	GENIC	homozygous	49874499
13	107545938	107545939	A	-	8	GENIC	homozygous	49874500
13	107546085	107546086	C	T	21	GENIC	heterozygous	49874501
13	107546087	107546088	C	T	22	GENIC	heterozygous	49874502
13	107546125	107546126	T	C	19	GENIC	heterozygous	49980701
13	107546127	107546128	T	C	18	GENIC	heterozygous	49874503
13	107546133	107546134	T	C	14	GENIC	homozygous	49874504
13	107546143	107546148	TGTTT	-----	9	GENIC	homozygous	49874505
13	107546149	107546151	AG	--	9	GENIC	homozygous	49874506
13	107546150	107546151	G	-	10	GENIC	possibly homozygous	49874507
13	107546152	107546153	G	-	10	GENIC	homozygous	49874508
13	107552015	107552016	T	-	12	GENIC	heterozygous	50371961
13	107552290	107552291	G	C	24	GENIC	homozygous	49874509
13	107589646	107589647	T	G	16	GENIC	homozygous	49874515
13	107589651	107589652	A	AG	11	GENIC	homozygous	49874516
13	107589696	107589697	T	TG	9	GENIC	homozygous	49874517
13	107503466	107503467	C	T	10	GENIC	heterozygous	50273208