chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	104037259	104037260	A	C	13	GENIC	homozygous	116961330
10	104037633	104037634	C	T	20	GENIC	homozygous	116961332
10	104038973	104038974	A	T	4	GENIC	homozygous	116834668
10	104039253	104039254	C	T	8	GENIC	homozygous	116961334
10	104039623	104039624	G	A	8	GENIC	homozygous	116834672
10	104039706	104039707	C	A	8	GENIC	heterozygous	116961336
10	104040527	104040528	C	A	11	GENIC	homozygous	116834676
10	104041653	104041654	T	C	10	GENIC	homozygous	126425863
10	104041916	104041917	G	A	20	GENIC	homozygous	116961338
10	104041941	104041942	G	C	18	GENIC	homozygous	116961340
10	104042056	104042057	C	T	10	GENIC	heterozygous	116961342
10	104043067	104043068	A	G	16	GENIC	homozygous	116834684
10	104043109	104043110	A	G	18	GENIC	homozygous	116961344
10	104043412	104043413	G	A	4	GENIC	homozygous	126391504
10	104043851	104043852	C	T	11	GENIC	homozygous	116834688
10	104044448	104044449	A	G	17	GENIC	homozygous	116834696
10	104044529	104044530	G	T	9	GENIC	homozygous	116961346
10	104044588	104044589	T	C	9	GENIC	homozygous	116834698
10	104045201	104045202	G	A	11	GENIC	homozygous	116961348
10	104046862	104046863	T	C	22	GENIC	homozygous	116834702
10	104047541	104047542	G	A	5	GENIC	homozygous	116961350
10	104049038	104049039	G	C	8	GENIC	homozygous	117347020
10	104050400	104050401	C	G	11	GENIC	homozygous	116961352
10	104050575	104050576	G	A	8	GENIC	homozygous	116961354
10	104050821	104050822	T	C	12	GENIC	homozygous	116834706
10	104051071	104051072	G	C	5	GENIC	homozygous	126391506
10	104051160	104051161	C	A	9	GENIC	homozygous	116834708
10	104051461	104051462	C	G	6	GENIC	homozygous	116834710
10	104051705	104051706	A	T	19	GENIC	homozygous	116834712
10	104052212	104052213	C	G	18	GENIC	homozygous	116834714
10	104052270	104052271	C	T	13	GENIC	homozygous	116834716