chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	107433313	107433314	T	C	16	GENIC	homozygous	116842391
10	107433418	107433419	T	C	16	GENIC	homozygous	116842393
10	107433600	107433601	A	G	25	GENIC	homozygous	116842395
10	107433686	107433687	C	T	19	GENIC	homozygous	116842397
10	107434166	107434167	C	T	13	GENIC	homozygous	117034016
10	107434704	107434705	T	C	11	GENIC	homozygous	117034018
10	107435571	107435572	T	G	19	GENIC	homozygous	116842403
10	107435802	107435803	T	G	19	GENIC	homozygous	117034020
10	107435947	107435948	C	T	23	GENIC	homozygous	117034022
10	107436641	107436642	A	G	16	GENIC	homozygous	117034024
10	107437292	107437293	A	G	17	GENIC	homozygous	117034026
10	107437749	107437750	A	C	14	GENIC	homozygous	116842407
10	107437901	107437902	C	G	15	GENIC	homozygous	116842409
10	107438113	107438114	C	T	15	GENIC	homozygous	116842411
10	107438169	107438170	A	G	13	GENIC	homozygous	116842413
10	107439218	107439219	T	C	14	GENIC	homozygous	117034028
10	107439379	107439380	C	T	14	GENIC	homozygous	116842417
10	107439610	107439611	G	C	19	GENIC	homozygous	116842419
10	107440533	107440534	G	A	19	GENIC	homozygous	116842421
10	107441263	107441264	G	A	19	GENIC	homozygous	116842423
10	107441732	107441733	T	A	18	GENIC	homozygous	116842425
10	107441894	107441895	A	G	14	GENIC	homozygous	116842427
10	107442181	107442182	G	A	20	GENIC	homozygous	116842429
10	107442270	107442271	C	T	12	GENIC	homozygous	116842431
10	107442368	107442369	G	A	12	GENIC	homozygous	116842433
10	107443300	107443301	G	A	15	GENIC	homozygous	116842435
10	107443893	107443899	AGGGGA		14	GENIC	homozygous	131099106
10	107437075	107437076	T	C	11	GENIC	homozygous	117261329
10	107443449	107443450	G	T	16	GENIC	homozygous	117261331
10	107442907	107442907		G	16	GENIC	homozygous	131099105
10	107444982	107444983	C	T	13	GENIC	homozygous	116842437
10	107435149	107435150	T		11	GENIC	homozygous	131471095
10	107435157	107435166	TCCCAGGCC		13	GENIC	homozygous	131471096
10	107445371	107445372	G	T	19	GENIC	homozygous	116842439