chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	55902848	55902849	T	C	19	GENIC	homozygous	116782972
10	55902897	55902898	G	A	22	GENIC	homozygous	116782974
10	55903222	55903223	C	T	22	GENIC	homozygous	116782976
10	55903350	55903351	C	G	26	GENIC	homozygous	116782978
10	55903654	55903655	T	G	30	GENIC	homozygous	116782980
10	55903861	55903862	C	T	22	GENIC	homozygous	116782982
10	55904102	55904103	A	T	37	GENIC	homozygous	116782984
10	55905079	55905080	G	T	33	GENIC	homozygous	116782986
10	55906918	55906919	G	A	18	GENIC	homozygous	117011547
10	55908336	55908337	C	T	31	GENIC	homozygous	116782990
10	55908754	55908755	G	A	24	GENIC	homozygous	116782992
10	55909077	55909078	G	A	21	GENIC	homozygous	116782994
10	55909138	55909139	G	A	21	GENIC	homozygous	116782996
10	55909375	55909376	G	A	15	GENIC	homozygous	116782998
10	55909897	55909898	T	C	38	GENIC	homozygous	116783002
10	55915554	55915555	T	C	39	GENIC	homozygous	116783004
10	55916495	55916496	G	A	35	GENIC	homozygous	116783006
10	55921177	55921178	G	A	24	GENIC	homozygous	116783008
10	55921392	55921393	C	T	30	GENIC	homozygous	116783010
10	55923158	55923159	A	G	35	GENIC	homozygous	116783012
10	55924238	55924239	G	A	27	GENIC	homozygous	116783014
10	55924684	55924685	C	A	12	GENIC	homozygous	116783016
10	55926591	55926592	A	C	22	GENIC	homozygous	116783018