chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	31858727	31858728	T	TA	28	GENIC	homozygous	50174531
12	31859615	31859616	A	ATT	24	GENIC	homozygous	50174534
12	31859766	31859767	T	C	22	GENIC	homozygous	50174536
12	31859941	31859942	C	T	31	GENIC	homozygous	50442010
12	31860519	31860520	G	A	34	GENIC	homozygous	50442012
12	31860632	31860633	G	C	28	GENIC	homozygous	50174537
12	31861277	31861278	T	-	21	GENIC	homozygous	50174538
12	31861789	31861790	T	TA	23	GENIC	homozygous	50442015
12	31862699	31862700	G	A	20	GENIC	homozygous	50442017
12	31862874	31862875	A	C	37	GENIC	homozygous	50442019
12	31863835	31863836	A	T	29	GENIC	homozygous	50174539
12	31864659	31864660	T	G	32	GENIC	homozygous	50174541
12	31865880	31865881	A	AT	7	GENIC	homozygous	50421410
12	31866911	31866914	AGC	---	30	GENIC	homozygous	50442021