Variant report

Variant	rs2630182
Chromosome Location	chr3:60055788-60055789
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs13060068	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs17061972	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs17257269	1.00[CHB][hapmap]
rs212010	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs212036	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs212038	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs2223085	1.00[ASN][1000 genomes]
rs2361336	1.00[JPT][hapmap]
rs2366953	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2630165	1.00[CHB][hapmap];0.88[GIH][hapmap];1.00[ASN][1000 genomes]
rs2630195	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2630205	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2736763	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2736776	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2736820	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34267930	0.89[ASN][1000 genomes]
rs3845974	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs4024129	1.00[JPT][hapmap]
rs4679629	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4679631	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4679636	1.00[JPT][hapmap]
rs6446109	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6446110	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs67136973	0.89[ASN][1000 genomes]
rs6773600	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6782148	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6789112	1.00[JPT][hapmap]
rs6791450	1.00[JPT][hapmap]
rs6794055	1.00[JPT][hapmap]
rs6797474	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6804216	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs6806074	1.00[JPT][hapmap]
rs7609578	1.00[JPT][hapmap]
rs7642268	1.00[JPT][hapmap]
rs9311748	0.89[ASN][1000 genomes]
rs969562	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs9833389	1.00[ASN][1000 genomes]
rs986651	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428085	chr3:59782509-60070116	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1014983	chr3:59884024-60558331	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv590387	chr3:59890976-60481459	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv834707	chr3:60005679-60184046	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv13593	chr3:60050980-60057155	Flanking Active TSS Enhancers Weak transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv18292	chr3:60055280-60057155	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60048800-60059400	Enhancers	Primary T helper cells fromperipheralblood	blood
2	chr3:60051600-60062000	Weak transcription	Aorta	Aorta
3	chr3:60051800-60056200	Weak transcription	Thymus	Thymus
4	chr3:60051800-60058200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr3:60051800-60063000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr3:60052000-60058400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr3:60052000-60059600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr3:60052200-60056600	Weak transcription	Fetal Thymus	thymus
9	chr3:60052200-60058000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr3:60052400-60055800	Weak transcription	Primary T cells from cord blood	blood
11	chr3:60055200-60055800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr3:60055400-60055800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr3:60055600-60055800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:60055600-60056400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
15	chr3:60055600-60056600	Genic enhancers	Primary T cells fromperipheralblood	blood
16	chr3:60055600-60056600	Genic enhancers	Dnd41	blood
17	chr3:60055600-60057600	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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