chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	42235292	42235293	A		45	GENIC	homozygous	139395556
14	42236877	42236877		ATAAA	49	GENIC	homozygous	139395557
14	42237649	42237650	A	G	46	GENIC	homozygous	139525289
14	42236618	42236619	A	G	54	GENIC	homozygous	139525286
14	42237030	42237031	T	C	54	GENIC	homozygous	139525287
14	42237464	42237465	G	A	42	GENIC	homozygous	139525288
14	42238130	42238131	A	T	50	GENIC	homozygous	139525290
14	42238509	42238510	C	T	44	GENIC	homozygous	139525291
14	42238683	42238683		CTTG	43	GENIC	homozygous	139395558
14	42239055	42239056	G	A	48	GENIC	homozygous	139525292
14	42239068	42239069	T	C	50	GENIC	homozygous	139525293
14	42239242	42239243	C	G	28	GENIC	homozygous	139525294
14	42239643	42239644	G	T	29	GENIC	homozygous	139525295
14	42239806	42239809	AAA		29	GENIC	homozygous	139395559
14	42239812	42239813	A	G	30	GENIC	homozygous	139525296
14	42239946	42239947	C	T	38	GENIC	homozygous	139525297
14	42240355	42240356	A	G	56	GENIC	homozygous	139525298
14	42241316	42241317	A	G	53	GENIC	homozygous	139525299