chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	154557263	154557264	A	G	10	GENIC	homozygous	110065383
2	154557396	154557397	C	T	15	GENIC	homozygous	110768588
2	154558141	154558142	G	A	9	GENIC	homozygous	110065385
2	154560882	154560883	T	C	19	GENIC	homozygous	110065387
2	154566172	154566173	T	C	9	GENIC	homozygous	110768594
2	154569147	154569148	C	G	15	GENIC	homozygous	110065397
2	154570831	154570832	C	T	12	GENIC	homozygous	110065400
2	154571107	154571108	G	A	6	GENIC	homozygous	110065402
2	154571452	154571453	T	C	11	GENIC	homozygous	110065406
2	154571943	154571944	C	T	14	GENIC	homozygous	110065408
2	154572018	154572019	C	T	6	GENIC	homozygous	110065410
2	154572144	154572145	A	G	2	GENIC	homozygous	110065412
2	154576208	154576209	G	A	11	GENIC	homozygous	110065414
2	154576382	154576383	G	A	18	GENIC	homozygous	110768596
2	154576937	154576938	C	T	14	GENIC	possibly homozygous	110768597
2	154577470	154577471	G	T	9	GENIC	homozygous	110598598
2	154577481	154577482	C	T	9	GENIC	homozygous	111331282
2	154578130	154578131	C	A	8	GENIC	homozygous	120127965
2	154578216	154578217	G	T	6	GENIC	homozygous	120127967
2	154578217	154578218	A	G	6	GENIC	homozygous	120127969
2	154578657	154578658	A	G	8	GENIC	homozygous	110065434
2	154582899	154582900	T	G	28	GENIC	homozygous	110768599
2	154583521	154583522	A	G	19	GENIC	homozygous	110065440
2	154583663	154583664	T	A	19	GENIC	homozygous	110065442
2	154586528	154586529	C	T	8	GENIC	homozygous	110768601
2	154587541	154587542	G	A	12	GENIC	homozygous	110065444
2	154589267	154589268	G	A	5	GENIC	homozygous	110768605
2	154589857	154589858	T	A	10	GENIC	homozygous	110065446