chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	23687431	23687432	T	C	83	GENIC	homozygous	48259327
15	23689548	23689549	T	C	51	GENIC	homozygous	48259332
15	23690787	23690788	A	G	47	GENIC	homozygous	48259335
15	23692526	23692527	C	T	53	GENIC	possibly homozygous	48475247
15	23692554	23692555	C	T	59	GENIC	homozygous	48475249
15	23692975	23692976	T	TA	13	GENIC	heterozygous	48259337
15	23692975	23692976	T	TAA	13	GENIC	heterozygous	48475251
15	23693065	23693066	A	G	31	GENIC	possibly homozygous	48259338
15	23693080	23693081	G	A	36	GENIC	possibly homozygous	48259339
15	23693161	23693162	A	G	61	GENIC	homozygous	48475253
15	23693193	23693194	T	TA	56	GENIC	possibly homozygous	48475255
15	23693447	23693448	G	A	61	GENIC	homozygous	48475257
15	23693667	23693668	T	C	83	GENIC	homozygous	48259342
15	23694776	23694777	A	C	66	GENIC	homozygous	48475259
15	23694805	23694806	T	G	61	GENIC	homozygous	48259344
15	23694814	23694815	C	T	60	GENIC	homozygous	48475261
15	23696325	23696326	T	A	45	GENIC	homozygous	48475263
15	23696806	23696807	A	G	42	GENIC	possibly homozygous	48475265
15	23696842	23696843	G	A	39	GENIC	possibly homozygous	48475267
15	23697080	23697081	A	T	66	GENIC	homozygous	48259348
15	23697106	23697107	G	T	72	GENIC	homozygous	48475269
15	23697347	23697348	T	TC	28	GENIC	homozygous	48259349
15	23697488	23697489	A	C	28	GENIC	homozygous	48259350