Joint Open Genome and Omics Platform (JoGo)

Search by Variant

Regionname

e.g. ALDH2_chr12_111761933_111822532, HBB_chr11_5220464_5232071.

Chr

Chromosome name (e.g., chr11).

Snpeff genename

Exact SnpEff gene name.

Sampleids

Target sampleid (e.g. HG02615).

Snpeff haplotype class

Haplotype-annotation class (e.g., ahapid, ahapid+chapid).

Snpeff annotation impact

Exact impact level (e.g., HIGH, MODERATE, LOW).

Snpeff annotation impact detail

Keyword match in SnpEff annotation.

Hapid

One or more haplotype IDs (comma-separated; e.g., a0001, a01, a0001c0001, a01c02, a1c2, a0001c0001t0005, a0001c0001t0005g0018).

Samplehapid

Sample haplotype IDs to include (comma-separated; e.g., HG02257.hp1, HG02615.hp2, HG00673.hp2).

No_hapid

Haplotype IDs to exclude (comma-separated; e.g., a0001, a0002, a0001c0001, a0001c0001t0005, a1, a01).

No_samplehapid

Sample haplotype IDs to exclude (comma-separated; e.g., HG02257.hp1, HG02615.hp2, HG00673.hp2).

Start

Start position (GRCh38).

End

End position (GRCh38).

Minac

Minimum alternate allele count (≥).

Maxac

Maximum alternate allele count (≤).

Minlen

Minimum variant length (≥).

Maxlen

Maximum variant length (≤).

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⚠️ Results limited to 10,000 hits. Refine your search for more specific results.

regionname	pos	ref	alt	annotation	impact	samples	ahapids	achapids	acthapids	actghapids	ac	an	af	hgvs_c	genename	geneid	featuretype	featureid	transcript_biotype	rank	distance	chr	external
AADAT_chr4_170055222_170094956	170060288	T T	A A	3_prime_UTR_variant 3_prime_UTR_variant	MODIFIER	NA18948.hp2 NA18948.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0008 a0001c0001t0008	a0001c0001t0008g0159 a0001c0001t0008g0159	1	378	0.0027	c.64 others(4): Show c.640A>T	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	13/13	640	chr4	TogoVar
AADAT_chr4_170055222_170094956	170060293	A A	G G	3_prime_UTR_variant 3_prime_UTR_variant	MODIFIER	NA18961.hp2 NA18961.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0006 a0001c0001t0006	a0001c0001t0006g0151 a0001c0001t0006g0151	1	378	0.0027	c.63 others(4): Show c.635T>C	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	13/13	635	chr4	TogoVar
AADAT_chr4_170055222_170094956	170060442	T T	C C	3_prime_UTR_variant 3_prime_UTR_variant	MODIFIER	NA18948.hp2 NA18948.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0008 a0001c0001t0008	a0001c0001t0008g0159 a0001c0001t0008g0159	1	378	0.0027	c.48 others(4): Show c.486A>G	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	13/13	486	chr4	TogoVar
AADAT_chr4_170055222_170094956	170060632	G G	T T	3_prime_UTR_variant 3_prime_UTR_variant	MODIFIER	HG00323.hp1 HG01255.hp2 HG01346.hp2 others(10): Show HG00323.hp1 HG01255.hp2 HG01346.hp2 HG01433.hp2 HG02451.hp1 HG02735.hp1 HG03041.hp2 HG03516.hp1 HG03831.hp1 NA18967.hp1 NA18983.hp1 NA20905.hp2 homoSapiens_chm13v2.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0002 a0001c0001t0002	a0001c0001t0002g0016 a0001c0001t0002g0053 a0001c0001t0002g0054 others(8): Show a0001c0001t0002g0016 a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0073 a0001c0001t0002g0100 a0001c0001t0002g0137 a0001c0001t0002g0204	13	378	0.0344	c.29 others(4): Show c.296C>A	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	13/13	296	chr4	TogoVar
AADAT_chr4_170055222_170094956	170060796	C C	A A	3_prime_UTR_variant 3_prime_UTR_variant	MODIFIER	HG00639.hp2 HG03195.hp2 HG00639.hp2 HG03195.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0004 a0001c0001t0004	a0001c0001t0004g0047 a0001c0001t0004g0047	2	378	0.0053	c.13 others(4): Show c.132G>T	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	13/13	132	chr4	TogoVar
AADAT_chr4_170055222_170094956	170060989	T T	A A	intron_variant intron_variant	MODIFIER	HG02630.hp2 HG03225.hp1 NA20129.hp1 HG02630.hp2 HG03225.hp1 NA20129.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0042 a0001c0001t0001g0186 a0001c0001t0001g0042 a0001c0001t0001g0186	3	378	0.0079	c.123 others(7): Show c.1237-20A>T	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	12/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170061166	G G	A A	intron_variant intron_variant	MODIFIER	HG01168.hp1 HG01169.hp1 HG01168.hp1 HG01169.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0034 a0001c0001t0001g0034	2	378	0.0053	c.123 others(8): Show c.1237-197C>T	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	12/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170061443	T T	C C	intron_variant intron_variant	MODIFIER	HG02273.hp2 HG02273.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0084 a0001c0001t0001g0084	1	378	0.0027	c.123 others(8): Show c.1236+449A>G	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	12/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170061535	C C	G G	intron_variant intron_variant	MODIFIER	HG03453.hp1 HG03453.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0198 a0001c0001t0001g0198	1	378	0.0027	c.123 others(8): Show c.1236+357G>C	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	12/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170061639	C C	T T	intron_variant intron_variant	MODIFIER	HG02451.hp2 HG02559.hp1 HG02717.hp1 others(9): Show HG02451.hp2 HG02559.hp1 HG02717.hp1 HG02723.hp1 HG02922.hp2 HG03130.hp1 HG03453.hp1 HG03453.hp2 HG03516.hp2 HG03579.hp1 NA19043.hp2 NA21309.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0001g0076 others(6): Show a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0138 a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0197 a0001c0001t0001g0198	12	378	0.0318	c.123 others(8): Show c.1236+253G>A	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	12/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170062318	T T	C C	intron_variant intron_variant	MODIFIER	HG02896.hp1 HG02896.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0052 a0001c0001t0001g0052	1	378	0.0027	c.113 others(8): Show c.1135-325A>G	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170062561	C C	T T	intron_variant intron_variant	MODIFIER	NA19074.hp1 NA19074.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0108 a0001c0001t0001g0108	1	378	0.0027	c.113 others(8): Show c.1135-568G>A	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170062676	C C	T T	intron_variant intron_variant	MODIFIER	HG02273.hp2 HG02738.hp1 HG02273.hp2 HG02738.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0084 a0001c0001t0001g0205 a0001c0001t0001g0084 a0001c0001t0001g0205	2	378	0.0053	c.113 others(8): Show c.1135-683G>A	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170062692	G G	C C	intron_variant intron_variant	MODIFIER	HG03471.hp2 HG03471.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0196 a0001c0001t0001g0196	1	378	0.0027	c.113 others(8): Show c.1135-699C>G	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170062709	G G	A A	intron_variant intron_variant	MODIFIER	HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show HG00099.hp2 HG00280.hp1 HG01070.hp2 HG01261.hp2 HG01515.hp2 HG01517.hp2 HG02004.hp1 HG02698.hp1 HG02735.hp2 HG04184.hp2 NA20805.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0194 others(3): Show a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0194 a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202	11	378	0.0291	c.113 others(8): Show c.1135-716C>T	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170062736	T T	C C	intron_variant intron_variant	MODIFIER	HG02622.hp1 HG02622.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0189 a0001c0001t0001g0189	1	378	0.0027	c.113 others(8): Show c.1135-743A>G	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170062771	T T	A A	intron_variant intron_variant	MODIFIER	HG02976.hp2 HG02976.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0061 a0001c0001t0001g0061	1	378	0.0027	c.113 others(8): Show c.1135-778A>T	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170063078	T T	C C	intron_variant intron_variant	MODIFIER	HG00735.hp1 HG00741.hp1 HG00735.hp1 HG00741.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0040 a0001c0001t0001g0040	2	378	0.0053	c.113 others(9): Show c.1135-1085A>G	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170063254	C C	T T	intron_variant intron_variant	MODIFIER	HG02717.hp1 HG02717.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0197 a0001c0001t0001g0197	1	378	0.0027	c.113 others(9): Show c.1135-1261G>A	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170063509	T T	C C	intron_variant intron_variant	MODIFIER	HG02109.hp2 HG02109.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0060 a0001c0001t0001g0060	1	378	0.0027	c.113 others(9): Show c.1134+1210A>G	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170063598	T T	C C	intron_variant intron_variant	MODIFIER	HG00323.hp1 HG02735.hp1 HG00323.hp1 HG02735.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0002 a0001c0001t0002	a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0002g0053 a0001c0001t0002g0057	2	378	0.0053	c.113 others(9): Show c.1134+1121A>G	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170063603	T T	C C	intron_variant intron_variant	MODIFIER	HG02559.hp1 HG02717.hp1 HG02723.hp1 others(7): Show HG02559.hp1 HG02717.hp1 HG02723.hp1 HG02922.hp2 HG03130.hp1 HG03453.hp1 HG03516.hp2 HG03579.hp1 NA19043.hp2 NA21309.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0015 a0001c0001t0001g0088 a0001c0001t0001g0138 others(4): Show a0001c0001t0001g0015 a0001c0001t0001g0088 a0001c0001t0001g0138 a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0197 a0001c0001t0001g0198	10	378	0.0265	c.113 others(9): Show c.1134+1116A>G	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170063631	A A	T T	intron_variant intron_variant	MODIFIER	NA19083.hp1 NA19083.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0150 a0001c0001t0001g0150	1	378	0.0027	c.113 others(9): Show c.1134+1088T>A	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170063674	C C	G G	intron_variant intron_variant	MODIFIER	HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00323.hp1 HG00408.hp1 HG00423.hp1 HG00423.hp2 HG00438.hp1 HG00438.hp2 HG00558.hp1 HG00558.hp2 HG00609.hp1 HG00621.hp1 HG00621.hp2 HG00639.hp2 HG00673.hp1 HG00673.hp2 HG00735.hp1 HG00741.hp1 HG00741.hp2 HG01069.hp1 HG01069.hp2 HG01070.hp2 HG01071.hp2 HG01109.hp2 HG01123.hp1 HG01123.hp2 HG01168.hp1 HG01168.hp2 HG01169.hp1 HG01169.hp2 HG01243.hp1 HG01255.hp2 HG01257.hp1 HG01258.hp2 HG01261.hp1 HG01261.hp2 HG01346.hp2 HG01358.hp2 HG01361.hp2 HG01433.hp2 HG01496.hp1 HG01496.hp2 HG01515.hp2 HG01516.hp1 HG01517.hp1 HG01517.hp2 HG01884.hp1 HG01928.hp1 HG01975.hp2 HG01978.hp1 HG02004.hp1 HG02015.hp2 HG02027.hp1 HG02080.hp1 HG02080.hp2 HG02129.hp1 HG02132.hp1 HG02132.hp2 HG02135.hp1 HG02258.hp1 HG02280.hp2 HG02293.hp1 HG02451.hp1 HG02523.hp1 HG02559.hp2 HG02602.hp1 HG02615.hp2 HG02698.hp1 HG02735.hp1 HG02735.hp2 HG02738.hp2 HG02895.hp1 HG02897.hp1 HG02965.hp1 HG03017.hp1 HG03041.hp2 HG03195.hp2 HG03490.hp1 HG03492.hp2 HG03516.hp1 HG03654.hp2 HG03669.hp2 HG03688.hp2 HG03704.hp1 HG03831.hp1 HG03834.hp1 HG03927.hp2 HG03942.hp2 HG04184.hp1 HG04184.hp2 HG04204.hp1 HG04228.hp1 HG04228.hp2 HG06807.hp2 NA18612.hp1 NA18941.hp1 NA18942.hp1 NA18942.hp2 NA18943.hp2 NA18944.hp1 NA18945.hp1 NA18946.hp2 NA18948.hp2 NA18949.hp2 NA18950.hp1 NA18951.hp2 NA18954.hp1 NA18955.hp2 NA18957.hp1 NA18957.hp2 NA18961.hp1 NA18961.hp2 NA18962.hp1 NA18963.hp2 NA18964.hp1 NA18967.hp1 NA18967.hp2 NA18968.hp1 NA18968.hp2 NA18969.hp1 NA18969.hp2 NA18970.hp1 NA18974.hp1 NA18974.hp2 NA18975.hp1 NA18978.hp2 NA18979.hp2 NA18981.hp2 NA18983.hp1 NA18983.hp2 NA18985.hp1 NA18985.hp2 NA18986.hp1 NA18986.hp2 NA18991.hp1 NA18991.hp2 NA18992.hp1 NA18993.hp2 NA18994.hp1 NA18994.hp2 NA18995.hp1 NA19000.hp1 NA19000.hp2 NA19001.hp1 NA19004.hp2 NA19005.hp1 NA19007.hp1 NA19009.hp1 NA19009.hp2 NA19054.hp1 NA19057.hp1 NA19058.hp1 NA19060.hp1 NA19060.hp2 NA19063.hp1 NA19065.hp1 NA19067.hp2 NA19068.hp1 NA19068.hp2 NA19070.hp1 NA19074.hp1 NA19075.hp1 NA19077.hp1 NA19079.hp2 NA19082.hp1 NA19082.hp2 NA19083.hp1 NA19084.hp2 NA19087.hp1 NA19087.hp2 NA19088.hp1 NA19091.hp2 NA19240.hp1 NA20752.hp2 NA20805.hp2 NA20905.hp2 NA21309.hp1 homoSapiens_chm13v2.hp1	a0001 a0001	a0001c0001 a0001c0002 a0001c0001 a0001c0002	a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(5): Show a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0008 a0001c0002t0001	a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0136 a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0002g0016 a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0073 a0001c0001t0002g0100 a0001c0001t0002g0137 a0001c0001t0002g0204 a0001c0001t0003g0010 a0001c0001t0003g0070 a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0164 a0001c0001t0003g0203 a0001c0001t0004g0047 a0001c0001t0006g0151 a0001c0001t0007g0063 a0001c0001t0008g0159 a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0142 a0001c0002t0001g0143 a0001c0002t0001g0144	179	378	0.4735	c.113 others(9): Show c.1134+1045G>C	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170063707	C C	T T	intron_variant intron_variant	MODIFIER	NA18942.hp2 NA18954.hp1 NA18942.hp2 NA18954.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0038 a0001c0001t0001g0038	2	378	0.0053	c.113 others(9): Show c.1134+1012G>A	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170063803	A A	G G	intron_variant intron_variant	MODIFIER	HG00423.hp2 HG00423.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0149 a0001c0001t0001g0149	1	378	0.0027	c.113 others(8): Show c.1134+916T>C	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170063871	G G	A A	intron_variant intron_variant	MODIFIER	HG00639.hp2 HG03195.hp2 HG00639.hp2 HG03195.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0004 a0001c0001t0004	a0001c0001t0004g0047 a0001c0001t0004g0047	2	378	0.0053	c.113 others(8): Show c.1134+848C>T	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170063967	A A	G G	intron_variant intron_variant	MODIFIER	HG02886.hp1 HG02886.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0062 a0001c0001t0001g0062	1	378	0.0027	c.113 others(8): Show c.1134+752T>C	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170064036	A A	G G	intron_variant intron_variant	MODIFIER	HG01884.hp1 HG01884.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0007 a0001c0001t0007	a0001c0001t0007g0063 a0001c0001t0007g0063	1	378	0.0027	c.113 others(8): Show c.1134+683T>C	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170064167	C C	G G	intron_variant intron_variant	MODIFIER	HG02258.hp1 HG02965.hp1 HG02258.hp1 HG02965.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0043 a0001c0001t0001g0043	2	378	0.0053	c.113 others(8): Show c.1134+552G>C	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170064193	C C	T T	intron_variant intron_variant	MODIFIER	NA19082.hp1 NA19082.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0163 a0001c0001t0001g0163	1	378	0.0027	c.113 others(8): Show c.1134+526G>A	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170064196	C C	T T	intron_variant intron_variant	MODIFIER	HG00738.hp2 HG00738.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0126 a0001c0001t0001g0126	1	378	0.0027	c.113 others(8): Show c.1134+523G>A	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170064247	T T	C C	intron_variant intron_variant	MODIFIER	HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00323.hp1 HG00408.hp1 HG00423.hp1 HG00423.hp2 HG00438.hp1 HG00438.hp2 HG00558.hp1 HG00558.hp2 HG00609.hp1 HG00621.hp1 HG00621.hp2 HG00639.hp2 HG00673.hp1 HG00673.hp2 HG00735.hp1 HG00738.hp2 HG00741.hp1 HG00741.hp2 HG01069.hp1 HG01069.hp2 HG01070.hp2 HG01071.hp2 HG01109.hp1 HG01109.hp2 HG01123.hp1 HG01123.hp2 HG01168.hp1 HG01168.hp2 HG01169.hp1 HG01169.hp2 HG01243.hp1 HG01255.hp2 HG01257.hp1 HG01258.hp2 HG01261.hp1 HG01261.hp2 HG01346.hp2 HG01358.hp2 HG01361.hp2 HG01433.hp2 HG01496.hp1 HG01496.hp2 HG01515.hp2 HG01516.hp1 HG01517.hp1 HG01517.hp2 HG01884.hp1 HG01884.hp2 HG01928.hp1 HG01975.hp2 HG01978.hp1 HG02004.hp1 HG02015.hp2 HG02027.hp1 HG02080.hp1 HG02080.hp2 HG02129.hp1 HG02132.hp1 HG02132.hp2 HG02135.hp1 HG02258.hp1 HG02280.hp2 HG02293.hp1 HG02451.hp1 HG02451.hp2 HG02523.hp1 HG02559.hp2 HG02572.hp1 HG02602.hp1 HG02615.hp2 HG02630.hp1 HG02630.hp2 HG02683.hp1 HG02698.hp1 HG02735.hp1 HG02735.hp2 HG02738.hp2 HG02818.hp2 HG02895.hp1 HG02896.hp2 HG02897.hp1 HG02897.hp2 HG02965.hp1 HG02976.hp2 HG03017.hp1 HG03041.hp2 HG03195.hp2 HG03225.hp1 HG03453.hp2 HG03486.hp1 HG03490.hp1 HG03491.hp1 HG03492.hp2 HG03516.hp1 HG03540.hp1 HG03579.hp2 HG03654.hp2 HG03669.hp2 HG03688.hp1 HG03688.hp2 HG03704.hp1 HG03831.hp1 HG03834.hp1 HG03927.hp2 HG03942.hp2 HG04184.hp1 HG04184.hp2 HG04204.hp1 HG04228.hp1 HG04228.hp2 HG06807.hp2 NA18522.hp1 NA18612.hp1 NA18612.hp2 NA18941.hp1 NA18942.hp1 NA18942.hp2 NA18943.hp2 NA18944.hp1 NA18945.hp1 NA18946.hp2 NA18948.hp2 NA18949.hp2 NA18950.hp1 NA18951.hp2 NA18954.hp1 NA18955.hp2 NA18957.hp1 NA18957.hp2 NA18961.hp1 NA18961.hp2 NA18962.hp1 NA18963.hp2 NA18964.hp1 NA18967.hp1 NA18967.hp2 NA18968.hp1 NA18968.hp2 NA18969.hp1 NA18969.hp2 NA18970.hp1 NA18974.hp1 NA18974.hp2 NA18975.hp1 NA18975.hp2 NA18978.hp2 NA18979.hp2 NA18981.hp2 NA18983.hp1 NA18983.hp2 NA18985.hp1 NA18985.hp2 NA18986.hp1 NA18986.hp2 NA18991.hp1 NA18991.hp2 NA18992.hp1 NA18992.hp2 NA18993.hp1 NA18993.hp2 NA18994.hp1 NA18994.hp2 NA18995.hp1 NA18995.hp2 NA19000.hp1 NA19000.hp2 NA19001.hp1 NA19004.hp2 NA19005.hp1 NA19007.hp1 NA19009.hp1 NA19009.hp2 NA19054.hp1 NA19057.hp1 NA19058.hp1 NA19060.hp1 NA19060.hp2 NA19063.hp1 NA19065.hp1 NA19066.hp2 NA19067.hp2 NA19068.hp1 NA19068.hp2 NA19070.hp1 NA19074.hp1 NA19074.hp2 NA19075.hp1 NA19077.hp1 NA19079.hp2 NA19082.hp1 NA19082.hp2 NA19083.hp1 NA19084.hp2 NA19087.hp1 NA19087.hp2 NA19088.hp1 NA19091.hp2 NA19240.hp1 NA20129.hp1 NA20752.hp2 NA20805.hp1 NA20805.hp2 NA20905.hp2 NA21309.hp1 homoSapiens_chm13v2.hp1	a0001 a0001	a0001c0001 a0001c0002 a0001c0001 a0001c0002	a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(5): Show a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0008 a0001c0002t0001	a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0076 a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0136 a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0002g0016 a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0073 a0001c0001t0002g0100 a0001c0001t0002g0137 a0001c0001t0002g0204 a0001c0001t0003g0010 a0001c0001t0003g0070 a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0164 a0001c0001t0003g0203 a0001c0001t0004g0047 a0001c0001t0006g0151 a0001c0001t0007g0063 a0001c0001t0008g0159 a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0142 a0001c0002t0001g0143 a0001c0002t0001g0144	208	378	0.5503	c.113 others(8): Show c.1134+472A>G	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170064258	A A	T T	intron_variant intron_variant	MODIFIER	HG03688.hp2 HG03688.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0153 a0001c0001t0001g0153	1	378	0.0027	c.113 others(8): Show c.1134+461T>A	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170064361	C C	T T	intron_variant intron_variant	MODIFIER	HG03654.hp1 HG03654.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0104 a0001c0001t0001g0104	1	378	0.0027	c.113 others(8): Show c.1134+358G>A	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170064436	T T	A A	intron_variant intron_variant	MODIFIER	HG02897.hp1 HG02897.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0176 a0001c0001t0001g0176	1	378	0.0027	c.113 others(8): Show c.1134+283A>T	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170064479	T T	C C	intron_variant intron_variant	MODIFIER	HG02897.hp1 HG02897.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0176 a0001c0001t0001g0176	1	378	0.0027	c.113 others(8): Show c.1134+240A>G	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170064688	G G	A A	intron_variant intron_variant	MODIFIER	HG02886.hp1 HG02886.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0062 a0001c0001t0001g0062	1	378	0.0027	c.113 others(7): Show c.1134+31C>T	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170064689	G G	T T	intron_variant intron_variant	MODIFIER	HG01978.hp2 HG01978.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0121 a0001c0001t0001g0121	1	378	0.0027	c.113 others(7): Show c.1134+30C>A	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	11/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170064834	A A	G G	intron_variant intron_variant	MODIFIER	HG02004.hp1 HG02004.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0201 a0001c0001t0001g0201	1	378	0.0027	c.102 others(6): Show c.1028-9T>C	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	10/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170065060	G G	A A	intron_variant intron_variant	MODIFIER	NA18949.hp2 NA19005.hp1 NA18949.hp2 NA19005.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0152 a0001c0001t0001g0154	2	378	0.0053	c.102 others(8): Show c.1028-235C>T	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	10/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170065129	T T	C C	intron_variant intron_variant	MODIFIER	HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show HG00099.hp2 HG00280.hp1 HG01070.hp2 HG01261.hp2 HG01515.hp2 HG01517.hp2 HG02004.hp1 HG02698.hp1 HG02735.hp2 HG04184.hp2 NA20805.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0194 others(3): Show a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0194 a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202	11	378	0.0291	c.102 others(8): Show c.1028-304A>G	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	10/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170065154	G G	A A	intron_variant intron_variant	MODIFIER	HG02451.hp2 HG03453.hp2 HG02451.hp2 HG03453.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0051 a0001c0001t0001g0076 a0001c0001t0001g0051 a0001c0001t0001g0076	2	378	0.0053	c.102 others(8): Show c.1028-329C>T	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	10/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170065157	A A	G G	intron_variant intron_variant	MODIFIER	HG01123.hp2 HG01123.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0148 a0001c0001t0001g0148	1	378	0.0027	c.102 others(8): Show c.1028-332T>C	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	10/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170065222	C C	G G	intron_variant intron_variant	MODIFIER	HG01109.hp1 HG02572.hp1 HG02818.hp2 others(3): Show HG01109.hp1 HG02572.hp1 HG02818.hp2 HG03540.hp1 HG03579.hp2 NA18522.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0007 a0001c0001t0001g0007	6	378	0.0159	c.102 others(8): Show c.1028-397G>C	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	10/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170065428	T T	G G	intron_variant intron_variant	MODIFIER	HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show HG00099.hp2 HG00280.hp1 HG01070.hp2 HG01261.hp2 HG01515.hp2 HG01517.hp2 HG02004.hp1 HG02698.hp1 HG02735.hp2 HG04184.hp2 NA20805.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0194 others(3): Show a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0194 a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202	11	378	0.0291	c.102 others(8): Show c.1028-603A>C	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	10/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170065509	G G	T T	intron_variant intron_variant	MODIFIER	HG00099.hp1 HG00099.hp1	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0185 a0001c0001t0001g0185	1	378	0.0027	c.102 others(8): Show c.1028-684C>A	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	10/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170065646	G G	A A	intron_variant intron_variant	MODIFIER	NA18522.hp2 NA18522.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0096 a0001c0001t0001g0096	1	378	0.0027	c.102 others(8): Show c.1027+768C>T	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	10/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170065654	T T	G G	intron_variant intron_variant	MODIFIER	HG03688.hp2 HG03688.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0153 a0001c0001t0001g0153	1	378	0.0027	c.102 others(8): Show c.1027+760A>C	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	10/12		chr4	TogoVar
AADAT_chr4_170055222_170094956	170066045	A A	G G	intron_variant intron_variant	MODIFIER	HG00099.hp2 HG00280.hp1 HG01070.hp2 others(8): Show HG00099.hp2 HG00280.hp1 HG01070.hp2 HG01261.hp2 HG01515.hp2 HG01517.hp2 HG02004.hp1 HG02698.hp1 HG02735.hp2 HG04184.hp2 NA20805.hp2	a0001 a0001	a0001c0001 a0001c0001	a0001c0001t0001 a0001c0001t0001	a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0194 others(3): Show a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0194 a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202	11	378	0.0291	c.102 others(8): Show c.1027+369T>C	AADAT	ENSG00000109576.14	transcript	ENST00000337664.9	protein_coding	10/12		chr4	TogoVar

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