chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40373377	40373378	G	GGC	16	GENIC	heterozygous	50512425
12	40373378	40373379	T	TTAGCGGTTAAGAG	16	GENIC	heterozygous	50512427
12	40373381	40373382	C	CTGA	15	GENIC	heterozygous	50543608
12	40373383	40373384	T	TGCTCTTCC	18	GENIC	heterozygous	50543609
12	40374839	40374840	C	-	25	GENIC	homozygous	50203426
12	40374851	40374852	T	C	28	GENIC	homozygous	50203427
12	40374856	40374857	T	-	28	GENIC	homozygous	50203428
12	40375108	40375109	A	G	41	GENIC	homozygous	50203429
12	40377124	40377125	C	T	47	GENIC	homozygous	50203430
12	40378101	40378102	T	C	53	GENIC	homozygous	50203431
12	40378558	40378559	G	GTT	24	GENIC	possibly homozygous	50203433
12	40379482	40379483	A	-	18	GENIC	possibly homozygous	50543610
12	40380441	40380443	TT	--	25	GENIC	possibly homozygous	50592125
12	40381874	40381875	T	TAC	19	GENIC	heterozygous	50203435
12	40381874	40381875	T	TACAC	19	GENIC	possibly homozygous	50203436
12	40382038	40382039	T	-	32	GENIC	homozygous	50203437
12	40382622	40382623	C	T	38	GENIC	homozygous	50203438
12	40384366	40384374	GACCACAC	--------	46	GENIC	homozygous	50203439
12	40385213	40385214	T	TAA	19	GENIC	possibly homozygous	50203440
12	40385213	40385214	T	TA	19	GENIC	heterozygous	50203441