chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	31151313	31151372	CGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAG		16	GENIC	homozygous	128803390
10	31167711	31167715	TTTG		42	GENIC	possibly homozygous	132881258
10	31170413	31170413		A	7	GENIC	homozygous	128803400
10	31170414	31170418	TCGC		7	GENIC	homozygous	128803401
10	31170421	31170424	ATC		8	GENIC	homozygous	128803402
10	31170427	31170436	GGGCTCTTT		8	GENIC	homozygous	128803403
10	31170440	31170441	G		8	GENIC	homozygous	128803404
10	31170446	31170447	T		8	GENIC	homozygous	128803405
10	31170449	31170450	T		8	GENIC	homozygous	128803406
10	31170451	31170452	G		8	GENIC	homozygous	128803407
10	31170458	31170459	C		8	GENIC	homozygous	128803408
10	31174597	31174598	A		9	GENIC	homozygous	128803409
10	31174601	31174602	A	C	9	GENIC	homozygous	123333686
10	31174609	31174610	C		12	GENIC	homozygous	128803410
10	31174617	31174619	CC		14	GENIC	homozygous	128803411
10	31174629	31174630	A		15	GENIC	homozygous	128803412
10	31174637	31174638	C		17	GENIC	homozygous	128803413
10	31174652	31174653	C		20	GENIC	homozygous	128803414
10	31174659	31174660	C		21	GENIC	homozygous	128803415
10	31174665	31174667	CT		22	GENIC	homozygous	128803416
10	31174682	31174682		A	24	GENIC	homozygous	128803417
10	31174685	31174686	T		25	GENIC	homozygous	128803418
10	31174692	31174693	T		26	GENIC	homozygous	128803419
10	31174697	31174698	C		28	GENIC	homozygous	128803420
10	31174716	31174717	C		30	GENIC	homozygous	128803421
10	31174722	31174722		A	32	GENIC	homozygous	128803422
10	31174727	31174728	T		31	GENIC	homozygous	128803423
10	31174729	31174730	T		31	GENIC	homozygous	128803424
10	31174734	31174737	GGC		32	GENIC	homozygous	128803425
10	31174743	31174744	A		33	GENIC	homozygous	128803426