chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	185288007	185288008	C	T	25	GENIC	homozygous	110164294
2	185288085	185288086	C	G	40	GENIC	homozygous	110164295
2	185288086	185288087	T	A	40	GENIC	homozygous	110164296
2	185288134	185288135	G	A	27	GENIC	homozygous	110164297
2	185288390	185288391	T	C	41	GENIC	homozygous	110164298
2	185288477	185288478	T	C	34	GENIC	possibly homozygous	120377369
2	185288559	185288560	A	C	28	GENIC	homozygous	110164299
2	185288667	185288668	A	G	34	GENIC	homozygous	110164300
2	185288751	185288752	C	T	27	GENIC	homozygous	110164301
2	185292995	185292996	G	A	12	GENIC	homozygous	110164303
2	185299206	185299207	T	A	31	GENIC	homozygous	110164304
2	185299809	185299810	C	T	20	GENIC	homozygous	110164305
2	185299938	185299939	G	T	20	GENIC	homozygous	110164306
2	185300173	185300174	T	C	24	GENIC	homozygous	110164307
2	185300416	185300417	C	T	24	GENIC	homozygous	110164308
2	185300435	185300436	A	G	25	GENIC	homozygous	110164309
2	185300508	185300509	C	T	27	GENIC	homozygous	110164310
2	185300866	185300867	C	T	29	GENIC	homozygous	110164311
2	185304440	185304441	A	G	20	GENIC	homozygous	110164312