chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39415326	39415327	G	A	16	GENIC	homozygous	50946451
12	39416061	39416062	T	C	16	GENIC	homozygous	50946454
12	39416708	39416709	T	C	10	GENIC	homozygous	50899697
12	39417171	39417172	A	C	11	GENIC	heterozygous	50946457
12	39417194	39417204	CAAAAAAAAC	----------	14	GENIC	homozygous	50946460
12	39417213	39417214	A	T	19	GENIC	homozygous	50899698
12	39417872	39417873	C	G	18	GENIC	homozygous	50199159
12	39418436	39418438	GA	--	10	GENIC	homozygous	50199161
12	39418439	39418445	TGATTG	------	9	GENIC	homozygous	50199163
12	39418948	39418949	T	TGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCA	9	GENIC	homozygous	50543016
12	39420195	39420196	T	TA	8	GENIC	homozygous	50511683
12	39420850	39420851	C	CTTTT	2	GENIC	heterozygous	50571296
12	39420865	39420874	GAGGCAGGG	---------	7	GENIC	heterozygous	50885484
12	39421208	39421209	A	G	20	GENIC	homozygous	50199173
12	39421269	39421271	GG	--	8	GENIC	heterozygous	50543018
12	39422998	39422999	G	A	15	GENIC	homozygous	50946463
12	39423256	39423257	C	T	25	GENIC	homozygous	50946466
12	39423484	39423610	TTTTTTTCGGAGCTGGGGACTGAACCCAGGACCTTGCGCTTGCTAGGCAAGTGCTCTACCACTGAGCTAAATCCCCAACCCCCCCCCCCCCCCGTTTAGTTTTTTTTTTTTTTTTTTTCCCGGTTC	------------------------------------------------------------------------------------------------------------------------------	11	GENIC	homozygous	50558895
12	39424014	39424015	T	-	2	GENIC	homozygous	50199187
12	39424929	39424930	A	G	19	GENIC	homozygous	50199193
12	39424972	39424973	G	T	25	GENIC	homozygous	50946469
12	39425488	39425489	C	CT	16	GENIC	homozygous	50199195
12	39425495	39425496	T	C	19	GENIC	homozygous	50199197
12	39425947	39425948	A	G	25	GENIC	possibly homozygous	50946472
12	39426065	39426066	C	G	26	GENIC	homozygous	50946475
12	39426545	39426546	C	T	10	GENIC	homozygous	50946477