chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	41911612	41911613	C	G	28	GENIC	homozygous	111105552
2	41911783	41911784	G	A	20	GENIC	homozygous	109715533
2	41912015	41912016	T	C	16	GENIC	homozygous	109715535
2	41913395	41913396	G	A	23	GENIC	possibly homozygous	109715537
2	41913461	41913462	G	A	26	GENIC	possibly homozygous	109715539
2	41914727	41914728	T	C	20	GENIC	homozygous	109715543
2	41916386	41916387	C	T	29	GENIC	possibly homozygous	109715545
2	41916397	41916398	G	A	26	GENIC	possibly homozygous	111105554
2	41912039	41912055	TTTTTTTTCTTTTTTC		12	GENIC	homozygous	130861540
2	41913390	41913390		A	22	GENIC	homozygous	130861541
2	41916849	41916849		T	12	GENIC	homozygous	127615990