chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	11257197	11257198	C	A	18	GENIC	homozygous	113962688
14	11259809	11259810	A	G	25	GENIC	homozygous	113340334
14	11260664	11260665	A	T	26	GENIC	homozygous	113941403
14	11260697	11260698	C	T	22	GENIC	homozygous	113340342
14	11261879	11261880	A	G	26	GENIC	homozygous	113340346
14	11262372	11262373	T	C	34	GENIC	homozygous	113340348
14	11262431	11262432	G	A	28	GENIC	homozygous	113941405
14	11262433	11262434	C	T	28	GENIC	homozygous	113340350
14	11263649	11263650	C	T	10	GENIC	homozygous	113340352
14	11264567	11264568	T	C	30	GENIC	homozygous	113340356
14	11264621	11264622	G	A	29	GENIC	homozygous	113340362
14	11265032	11265033	T	A	19	GENIC	homozygous	113941408
14	11265249	11265250	C	G	21	GENIC	homozygous	113340366
14	11265401	11265402	G	A	28	GENIC	homozygous	113340368
14	11266084	11266085	C	T	31	GENIC	homozygous	113941410
14	11266791	11266792	T	C	19	GENIC	homozygous	113340372
14	11268978	11268979	A	G	20	GENIC	homozygous	113340379
14	11269349	11269350	G	C	25	GENIC	homozygous	113941412
14	11269366	11269367	G	A	28	GENIC	homozygous	113941414
14	11269379	11269380	C	T	36	GENIC	homozygous	113340383
14	11269395	11269396	G	A	31	GENIC	homozygous	113340385
14	11269444	11269445	C	T	32	GENIC	homozygous	113941416
14	11269455	11269456	G	A	35	GENIC	homozygous	113941418
14	11269984	11269985	T	C	41	GENIC	homozygous	113340387
14	11270801	11270802	A	G	31	GENIC	homozygous	113340389
14	11271339	11271340	T	C	17	GENIC	homozygous	113340393
14	11272775	11272776	G	A	17	GENIC	homozygous	113941420
14	11272790	11272791	C	T	19	GENIC	homozygous	113941422
14	11273585	11273586	T	C	17	GENIC	homozygous	113941424