chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	98387444	98387445	C	G	50	GENIC	homozygous	113936253
5	98388472	98388473	T	C	41	GENIC	homozygous	113936254
5	98391149	98391150	G	T	21	GENIC	homozygous	113936255
5	98391361	98391362	A	G	12	GENIC	homozygous	113936256
5	98391381	98391382	T	C	8	GENIC	homozygous	113936257
5	98391436	98391437	C	A	13	GENIC	homozygous	113936258
5	98391764	98391765	G	A	15	GENIC	homozygous	113936259
5	98392225	98392226	C	T	33	GENIC	homozygous	113936260
5	98392639	98392640	T	A	39	GENIC	homozygous	113936261
5	98392818	98392819	C	T	49	GENIC	homozygous	113936262
5	98392819	98392820	C	G	50	GENIC	homozygous	113936263
5	98393039	98393040	G	T	34	GENIC	homozygous	113936264
5	98393724	98393725	C	A	47	GENIC	homozygous	113936265
5	98394084	98394085	A	G	51	GENIC	homozygous	113936266
5	98394567	98394568	A	G	30	GENIC	homozygous	113936267
5	98395800	98395801	T	C	26	GENIC	homozygous	113936268
5	98396424	98396425	G	T	17	GENIC	homozygous	113936269
5	98396425	98396426	C	T	17	GENIC	homozygous	113936270
5	98397991	98397992	C	T	14	GENIC	homozygous	113936271
5	98399942	98399943	G	A	17	GENIC	homozygous	113936272
5	98402341	98402342	G	A	22	GENIC	homozygous	113936274
5	98403255	98403256	G	A	37	GENIC	homozygous	113936275
5	98403495	98403496	T	C	18	GENIC	homozygous	118844368
5	98403927	98403928	C	T	28	GENIC	homozygous	113936276
5	98404765	98404766	A	T	36	GENIC	homozygous	113936277
5	98405246	98405247	A	T	33	GENIC	homozygous	113936278
5	98405761	98405762	T	C	11	GENIC	homozygous	113936279
5	98405821	98405822	G	A	21	GENIC	homozygous	113936280
5	98406035	98406036	C	T	23	GENIC	homozygous	113936281