chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	184172335	184172336	T	C	69	GENIC	homozygous	136405204
2	184173201	184173201		TG	50	GENIC	homozygous	135966383
2	184173652	184173653	T	C	63	GENIC	homozygous	136405206
2	184173836	184173837	G	A	54	GENIC	homozygous	136405207
2	184174055	184174056	G	A	75	GENIC	homozygous	136405208
2	184174389	184174389		T	56	GENIC	homozygous	135966384
2	184175146	184175147	T	C	52	GENIC	homozygous	136405209
2	184176076	184176077	A	G	56	GENIC	homozygous	136405210
2	184176642	184176643	A	G	35	GENIC	homozygous	136405212
2	184175713	184175714	C	T	46	GENIC	homozygous	141423353
2	184176334	184176335	C	T	56	GENIC	homozygous	136405211
2	184177242	184177243	A	C	42	GENIC	possibly homozygous	136405213
2	184177261	184177262	G	A	49	GENIC	possibly homozygous	136405214
2	184177366	184177367	T	C	56	GENIC	homozygous	136405215
2	184178078	184178079	G	A	44	GENIC	homozygous	136405217
2	184178104	184178104		A	34	GENIC	homozygous	135966385
2	184178158	184178159	T	C	49	GENIC	homozygous	136405218
2	184178178	184178179	C	T	51	GENIC	homozygous	136405219
2	184178224	184178225	T	G	63	GENIC	homozygous	136405220
2	184178556	184178557	A	G	54	GENIC	homozygous	136405221
2	184178623	184178624	T		41	GENIC	homozygous	135966386
2	184178733	184178734	G	A	45	GENIC	homozygous	141423354
2	184178873	184178874	C	T	45	GENIC	homozygous	136405222
2	184179070	184179071	C	T	47	GENIC	homozygous	136405223
2	184179102	184179103	C	T	39	GENIC	homozygous	136405224
2	184179699	184179700	C	T	35	GENIC	homozygous	136405226
2	184179725	184179725		T	37	GENIC	possibly homozygous	135966387
2	184179836	184179837	T	G	62	GENIC	homozygous	136405228
2	184179861	184179862	A	G	61	GENIC	homozygous	136405229
2	184180511	184180512	A	G	46	GENIC	homozygous	136405230
2	184180758	184180759	T	C	34	GENIC	homozygous	136405231
2	184179912	184179926	CTTGATGACAGTGC		57	GENIC	homozygous	141334529