chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	52498328	52498329	G		20	GENIC	homozygous	135907211
2	52498481	52498482	T	A	30	GENIC	homozygous	136108237
2	52499005	52499006	A	G	32	GENIC	homozygous	136108238
2	52499139	52499140	T	C	20	GENIC	homozygous	136108239
2	52499348	52499349	A	G	20	GENIC	homozygous	136108240
2	52499523	52499523		C	20	GENIC	homozygous	135907212
2	52499720	52499721	G	T	22	GENIC	homozygous	136108241
2	52499946	52499947	T	C	22	GENIC	homozygous	136108242
2	52500035	52500036	T	C	18	GENIC	homozygous	136108243
2	52500136	52500137	A		24	GENIC	homozygous	135907213
2	52500798	52500798		T	8	GENIC	homozygous	135907214
2	52500802	52500803	C	T	8	GENIC	homozygous	136108244
2	52500808	52500809	C	T	5	GENIC	homozygous	136108245
2	52500811	52500812	C	T	15	GENIC	homozygous	136108246
2	52500817	52500818	C	T	14	GENIC	homozygous	136108247
2	52501045	52501046	T	C	21	GENIC	homozygous	136108248
2	52503732	52503733	C	T	21	GENIC	homozygous	136108249
2	52504321	52504322	A	T	24	GENIC	homozygous	136108250
2	52504559	52504559		A	13	GENIC	homozygous	135907215
2	52504871	52504872	G	A	18	GENIC	homozygous	136108251
2	52505301	52505302	T		16	GENIC	homozygous	135907216
2	52507861	52507862	C	T	17	GENIC	homozygous	136108252
2	52508276	52508277	C	T	18	GENIC	homozygous	136108253
2	52508407	52508408	A	G	20	GENIC	homozygous	136108254