chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	26322628	26322630	TT	--	28	GENIC	heterozygous	50147539
12	26322629	26322630	T	-	28	GENIC	heterozygous	50147540
12	26322686	26322687	A	T	35	GENIC	homozygous	50147542
12	26323097	26323098	A	C	43	GENIC	homozygous	50147544
12	26323193	26323194	T	C	40	GENIC	homozygous	50147546
12	26323265	26323266	G	-	36	GENIC	homozygous	50147548
12	26323334	26323430	TTTTCAGTTTCCCTCTTTTTTTTTTTTTTTTTTTTTTTTATGTTAATCGTTGATGTTCTTGTTTTTTGTTTTTGTTTTTTTTATTAACTTGAGTAT	------------------------------------------------------------------------------------------------	29	GENIC	homozygous	50569552
12	26323970	26323971	T	C	43	GENIC	homozygous	50147550
12	26324285	26324286	C	T	48	GENIC	homozygous	50147552
12	26325403	26325404	C	G	37	GENIC	homozygous	50147554
12	26325626	26325634	TTTTTTTT	--------	12	GENIC	heterozygous	50614685
12	26325629	26325634	TTTTT	-----	12	GENIC	heterozygous	50539331
12	26326225	26326226	T	C	31	GENIC	homozygous	50147558
12	26326415	26326416	A	G	22	GENIC	homozygous	50147560
12	26326905	26326906	A	C	46	GENIC	homozygous	50147562
12	26328596	26328597	G	T	34	GENIC	homozygous	50147564
12	26329440	26329441	T	C	45	GENIC	homozygous	50147566
12	26329636	26329637	T	-	15	GENIC	homozygous	50539333
12	26333171	26333172	C	T	30	GENIC	homozygous	50147570
12	26333453	26333454	G	A	38	GENIC	homozygous	50147572
12	26333483	26333484	C	T	41	GENIC	homozygous	50147574
12	26334167	26334168	T	C	41	GENIC	homozygous	50147576
12	26334825	26334826	C	A	50	GENIC	homozygous	50147578
12	26335201	26335202	T	TTG	20	GENIC	heterozygous	50539334
12	26335248	26335249	T	TGTGTGTGTG	35	GENIC	heterozygous	50569553
12	26336017	26336018	T	TACAC	39	GENIC	homozygous	50147580
12	26336646	26336647	G	GGA	46	GENIC	heterozygous	50569554
12	26336648	26336649	C	CTGGGGGTTGGTGTGATA	47	GENIC	heterozygous	50569555
12	26336650	26336651	C	CAGTCTGGTCTCTAACTCTTCT	49	GENIC	heterozygous	50569556