chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	144526537	144526538	G	A	25	GENIC	homozygous	110039281
2	144527708	144527709	A	G	9	GENIC	homozygous	110039282
2	144527712	144527713	G	C	9	GENIC	homozygous	110039283
2	144527789	144527790	C	T	4	GENIC	homozygous	110039284
2	144530102	144530103	G	A	21	GENIC	homozygous	110039285
2	144532102	144532103	A	G	21	GENIC	homozygous	110039287
2	144533540	144533541	C	T	23	GENIC	homozygous	110039288
2	144533628	144533629	A	C	17	GENIC	homozygous	110039289
2	144534638	144534639	A	G	22	GENIC	homozygous	110039290
2	144536158	144536159	G	A	22	GENIC	homozygous	110039291
2	144536171	144536172	G	C	20	GENIC	homozygous	110039292
2	144536176	144536177	T	C	20	GENIC	homozygous	110039293
2	144536206	144536207	G	A	19	GENIC	homozygous	110039294
2	144537047	144537048	G	C	8	GENIC	homozygous	110039295
2	144537049	144537050	G	C	8	GENIC	homozygous	110039296
2	144537051	144537052	G	C	9	GENIC	homozygous	110039297
2	144537265	144537266	C	G	17	GENIC	homozygous	120127346
2	144537266	144537267	G	C	17	GENIC	homozygous	120127347
2	144537476	144537477	G	T	8	GENIC	homozygous	110039298
2	144537704	144537705	C	T	21	GENIC	homozygous	110039299
2	144541712	144541713	C	T	20	GENIC	homozygous	110039300
2	144542304	144542305	G	C	22	GENIC	homozygous	110039302
2	144542337	144542338	G	C	22	GENIC	homozygous	110039303
2	144544312	144544313	T	C	30	GENIC	homozygous	110039304
2	144545496	144545497	T	C	21	GENIC	homozygous	110039305