chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	154520663	154520664	A	G	41	GENIC	homozygous	110065337
2	154521832	154521833	G	A	44	GENIC	homozygous	110065339
2	154523478	154523479	G	A	28	GENIC	homozygous	110065341
2	154530148	154530149	T	A	36	GENIC	homozygous	110065346
2	154531851	154531851		A	47	GENIC	possibly homozygous	127693031
2	154523295	154523295		G	35	GENIC	homozygous	127693029
2	154525269	154525269		AG	35	GENIC	homozygous	127693030
2	154533192	154533193	C	T	35	GENIC	homozygous	110065350
2	154534203	154534204	C	G	51	GENIC	homozygous	110065352
2	154534992	154534993	G	A	49	GENIC	homozygous	110065354
2	154535842	154535843	G	A	49	GENIC	homozygous	110065355
2	154538080	154538081	T	C	42	GENIC	homozygous	110065357
2	154538184	154538185	T	C	40	GENIC	homozygous	110065359
2	154539332	154539333	A	G	47	GENIC	homozygous	110065361
2	154536777	154536778	T	A	22	GENIC	heterozygous	120150926
2	154536779	154536780	T	A	25	GENIC	homozygous	120150927
2	154536781	154536782	T	A	25	GENIC	homozygous	120150928