chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	94169905	94169906	T	-	21	GENIC	homozygous	49966930
13	94170093	94170094	C	G	22	GENIC	homozygous	49966931
13	94170145	94170146	C	CT	12	GENIC	homozygous	49966932
13	94170798	94170799	T	C	26	GENIC	homozygous	49966934
13	94171803	94171804	A	AT	15	GENIC	homozygous	49966935
13	94173195	94173196	A	AT	28	GENIC	homozygous	49966936
13	94173934	94173941	ACCATCC	-------	12	GENIC	homozygous	49966938
13	94176331	94176349	TCATCATCATCATCATCA	------------------	9	GENIC	homozygous	50958973
13	94177379	94177380	A	-	19	GENIC	possibly homozygous	50730574
13	94180759	94180760	C	A	25	GENIC	homozygous	50983206
13	94170356	94170357	T	TTA	5	GENIC	homozygous	50983201
13	94178379	94178380	C	CGTGTGTGTGTGTGT	13	GENIC	homozygous	50983202
13	94179490	94179491	G	A	21	GENIC	homozygous	50983203
13	94179927	94179928	C	T	18	GENIC	homozygous	50983204
13	94179935	94179949	CACACACACACACA	--------------	10	GENIC	homozygous	50983205
13	94182241	94182242	T	C	26	GENIC	homozygous	50983207
13	94183227	94183228	T	-	20	GENIC	possibly homozygous	49966943
13	94184833	94184834	G	A	15	GENIC	homozygous	50983208
13	94185773	94185774	C	-	9	GENIC	homozygous	50983209
13	94186128	94186129	G	A	9	GENIC	homozygous	50730577
13	94187904	94187905	A	AGAGGGGGAGGGGGAGGAAGAGGAGGGGAGAAGGAGAAGGAGGAGGGAGGAGGAGGGAGG	7	GENIC	homozygous	50530967
13	94191182	94191183	G	GTGTCTGTC	3	GENIC	heterozygous	51141178
13	94191738	94191739	G	A	23	GENIC	homozygous	50983210
13	94192539	94192540	T	C	6	GENIC	homozygous	49966946
13	94191414	94191420	ACACAC	------	5	GENIC	homozygous	50658707
13	94191188	94191189	G	GTCTGTC	3	GENIC	heterozygous	51185571