chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	23686098	23686099	T	C	18	GENIC	homozygous	48259325
15	23686259	23686260	A	-	25	GENIC	heterozygous	49040559
15	23686278	23686279	A	-	29	GENIC	heterozygous	48949343
15	23686361	23686362	A	ATT	26	GENIC	heterozygous	48949345
15	23686391	23686392	T	TG	17	GENIC	heterozygous	48949347
15	23686422	23686423	A	AATAAAGCCTT	16	GENIC	heterozygous	49040561
15	23686430	23686434	CAAG	----	15	GENIC	heterozygous	49040563
15	23687012	23687013	A	G	23	GENIC	homozygous	48259326
15	23687431	23687432	T	C	23	GENIC	homozygous	48259327
15	23687788	23687789	C	T	16	GENIC	homozygous	48259328
15	23687854	23687855	G	A	13	GENIC	homozygous	48259329
15	23687889	23687890	C	G	15	GENIC	homozygous	48259330
15	23689047	23689048	A	-	25	GENIC	homozygous	48259331
15	23689548	23689549	T	C	21	GENIC	homozygous	48259332
15	23689779	23689780	T	C	29	GENIC	homozygous	48259333
15	23690472	23690473	A	G	22	GENIC	homozygous	48259334
15	23690787	23690788	A	G	20	GENIC	homozygous	48259335
15	23692294	23692295	A	AT	16	GENIC	homozygous	48259336
15	23692975	23692976	T	TA	7	GENIC	homozygous	48259337
15	23693065	23693066	A	G	9	GENIC	homozygous	48259338
15	23693080	23693081	G	A	10	GENIC	homozygous	48259339
15	23693318	23693319	G	A	16	GENIC	homozygous	48259340
15	23693322	23693323	G	A	16	GENIC	homozygous	48259341
15	23693667	23693668	T	C	18	GENIC	homozygous	48259342
15	23694153	23694154	A	ACT	23	GENIC	homozygous	48259343
15	23694805	23694806	T	G	14	GENIC	homozygous	48259344
15	23695475	23695476	C	T	16	GENIC	homozygous	48259345
15	23696004	23696005	C	T	20	GENIC	homozygous	48259346
15	23696134	23696135	A	G	16	GENIC	homozygous	48259347
15	23697080	23697081	A	T	10	GENIC	homozygous	48259348
15	23697347	23697348	T	TC	4	GENIC	homozygous	48259349
15	23693555	23693556	C	-	20	GENIC	heterozygous	49117980
15	23693582	23693583	G	GA	17	GENIC	heterozygous	49117982