chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	37092798	37092799	A	G	38	GENIC	homozygous	48501197
15	37093550	37093551	G	A	31	GENIC	homozygous	48501199
15	37095545	37095546	T	-	2	GENIC	homozygous	48501201
15	37095751	37095752	T	A	42	GENIC	possibly homozygous	48501203
15	37096010	37096011	C	CTT	22	GENIC	homozygous	48501205
15	37096121	37096122	G	A	34	GENIC	possibly homozygous	48501207
15	37096271	37096272	T	C	29	GENIC	homozygous	48501209
15	37097418	37097432	GACCGCTTTAGCCC	--------------	8	GENIC	homozygous	48501211
15	37097420	37097423	CCG	---	8	GENIC	homozygous	48501213
15	37097633	37097634	C	-	18	GENIC	homozygous	48501215
15	37098209	37098210	G	T	24	GENIC	homozygous	48501217
15	37098427	37098428	C	T	23	GENIC	homozygous	48501219
15	37098649	37098650	C	A	37	GENIC	homozygous	48501221
15	37098817	37098818	A	G	46	GENIC	homozygous	48501223
15	37098888	37098889	G	T	34	GENIC	homozygous	48501225
15	37098910	37098911	A	-	26	GENIC	homozygous	48501227
15	37099021	37099022	G	GA	35	GENIC	homozygous	48501229
15	37099230	37099231	T	C	27	GENIC	homozygous	48501232
15	37099602	37099603	A	G	35	GENIC	homozygous	48501234
15	37099609	37099610	G	A	32	GENIC	homozygous	48501236
15	37099793	37099794	T	C	39	GENIC	homozygous	48501238
15	37099958	37099959	T	C	30	GENIC	homozygous	48501240
15	37100075	37100076	A	G	34	GENIC	homozygous	48501242
15	37100850	37100851	T	G	15	GENIC	homozygous	48501246
15	37101158	37101159	C	T	21	GENIC	homozygous	48501248
15	37102843	37102844	A	C	38	GENIC	homozygous	48501251
15	37103273	37103274	C	G	27	GENIC	homozygous	48501253