chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42479561	42479562	A	T	13	GENIC	homozygous	50209153
12	42480660	42480661	C	CCA	8	GENIC	heterozygous	50209156
12	42480660	42480661	C	CCACA	8	GENIC	heterozygous	50544348
12	42483114	42483157	AGATGGGTGCTCTTAACCGCTGAGCCATCTCTCCAGCCCCCCC	-------------------------------------------	12	GENIC	heterozygous	50544349
12	42483368	42483369	T	-	16	GENIC	heterozygous	50563858
12	42483954	42483955	T	-	7	GENIC	heterozygous	50563860
12	42486270	42486271	A	AC	4	INTERGENIC	homozygous	50209165
12	42483953	42483955	TT	--	7	GENIC	heterozygous	50572255
12	42487729	42487730	T	C	13	GENIC	homozygous	50209169
12	42488412	42488421	TTTTTTTAA	---------	2	GENIC	heterozygous	50209173
12	42488606	42488607	C	T	13	GENIC	homozygous	50563866
12	42488909	42488910	A	T	36	GENIC	homozygous	50563868
12	42489036	42489037	C	T	33	GENIC	homozygous	50563870
12	42489914	42489915	C	T	47	GENIC	possibly homozygous	50563872
12	42490252	42490253	G	-	35	GENIC	homozygous	50592216
12	42490538	42490539	A	G	27	GENIC	homozygous	50209176
12	42486435	42486436	C	G	8	INTERGENIC	homozygous	50804593
12	42484990	42484994	GTGT	----	5	GENIC	heterozygous	50804591
12	42488256	42488257	A	G	27	GENIC	homozygous	50804595
12	42490657	42490658	C	T	34	GENIC	homozygous	50209180
12	42490876	42490877	A	C	47	GENIC	homozygous	50563880
12	42491393	42491394	C	T	22	GENIC	homozygous	50209181
12	42493649	42493650	T	C	34	INTERGENIC	homozygous	50592219
12	42493679	42493680	G	A	34	INTERGENIC	homozygous	50804597
12	42493899	42493900	C	T	28	INTERGENIC	possibly homozygous	50592220
12	42494101	42494102	C	A	28	INTERGENIC	homozygous	50209183
12	42494157	42494158	A	G	27	INTERGENIC	homozygous	50209184
12	42490598	42490603	CACGC	-----	15	GENIC	heterozygous	50885553
12	42490596	42490603	CACACGC	-------	15	GENIC	heterozygous	50885551