chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	225037098	225037099	C	G	62	GENIC	homozygous	108556402
1	225038486	225038622	GCAAGTCCTACTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTCCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC		49	GENIC	possibly homozygous	131782848
1	225038800	225038801	C	T	68	GENIC	homozygous	108556404
1	225039207	225039208	A	G	71	GENIC	homozygous	108556405
1	225040135	225040136	T	C	69	GENIC	homozygous	108556406
1	225040274	225040275	A	G	58	GENIC	homozygous	108556408
1	225044595	225044596	G	T	47	GENIC	homozygous	108556411
1	225044729	225044730	A	G	47	GENIC	homozygous	108556412
1	225043625	225043626	C	T	55	GENIC	homozygous	120595328
1	225038185	225038185		C	75	GENIC	homozygous	130833549
1	225038292	225038296	AAAG		49	GENIC	homozygous	127487465
1	225039784	225039785	G		17	GENIC	homozygous	127487466
1	225043565	225043566	C		55	GENIC	homozygous	127487467
1	225039785	225039786	C	A	17	GENIC	homozygous	120476030