chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	14923711	14923712	T	C	11	GENIC	homozygous	50799307
12	14925241	14925242	G	GCT	6	GENIC	homozygous	50799309
12	14925594	14925595	C	CACAT	7	GENIC	heterozygous	50993183
12	14925598	14925599	T	TACATAC	7	GENIC	possibly homozygous	50799311
12	14925655	14925660	TACTG	-----	7	GENIC	homozygous	50799313
12	14925753	14925754	T	C	5	GENIC	homozygous	50799315
12	14926066	14926067	A	T	9	GENIC	homozygous	50799317
12	14926191	14926192	C	-	2	GENIC	homozygous	50716543
12	14926963	14926964	G	-	1	GENIC	homozygous	50923456
12	14930682	14930683	T	C	11	GENIC	homozygous	50799319
12	14933618	14933620	CA	--	2	GENIC	homozygous	50799322
12	14936208	14936248	GACGGCCTCTGCATCCCACTGACGGCCTCTGCATCCCACT	----------------------------------------	5	GENIC	homozygous	50533337
12	14938923	14938924	C	T	9	GENIC	homozygous	50069994
12	14939952	14939962	CACACACACA	----------	2	GENIC	homozygous	50533339
12	14943066	14943067	T	TGTGTGTGTGTGTGTGC	2	GENIC	homozygous	50560547
12	14943336	14943337	A	G	10	GENIC	homozygous	50069998
12	14945130	14945131	C	T	8	GENIC	homozygous	50070000
12	14945545	14945546	G	A	10	GENIC	homozygous	50070002
12	14945813	14945814	C	A	10	GENIC	homozygous	50070004
12	14945902	14945903	G	A	11	GENIC	homozygous	50070006
12	14945912	14945913	C	T	11	GENIC	homozygous	50070008
12	14946462	14946463	T	G	4	GENIC	homozygous	50070010
12	14950600	14950601	A	-	7	GENIC	heterozygous	50434934
12	14951433	14951434	A	G	7	GENIC	homozygous	50070012
12	14951471	14951472	C	T	6	GENIC	homozygous	50070014