Variant report

Variant	rs11182704
Chromosome Location	chr12:45220287-45220288
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10506259	1.00[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10880694	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10880698	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10880699	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10880727	1.00[AMR][1000 genomes]
rs10880728	1.00[AMR][1000 genomes]
rs10880729	1.00[AMR][1000 genomes]
rs11182700	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs11182709	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182712	1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11182713	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11182714	1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11182717	1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11182722	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11182723	0.89[ASN][1000 genomes]
rs11182724	1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11182725	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11182726	0.89[ASN][1000 genomes]
rs11182728	0.83[ASN][1000 genomes]
rs11182729	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11182730	1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11182732	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11182770	1.00[AMR][1000 genomes]
rs11182771	1.00[AMR][1000 genomes]
rs11182772	1.00[AMR][1000 genomes]
rs11182785	1.00[AMR][1000 genomes]
rs11182789	1.00[AMR][1000 genomes]
rs11182790	1.00[AMR][1000 genomes]
rs11182791	1.00[AMR][1000 genomes]
rs11182792	1.00[AMR][1000 genomes]
rs11182793	1.00[AMR][1000 genomes]
rs11182796	1.00[CHB][hapmap];0.92[JPT][hapmap];0.87[AMR][1000 genomes]
rs11534985	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12227311	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12227622	1.00[CHB][hapmap];0.89[AMR][1000 genomes]
rs12228073	1.00[CHB][hapmap];1.00[AMR][1000 genomes]
rs12228476	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12580287	1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12581903	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12582602	1.00[AMR][1000 genomes]
rs12829945	0.89[AMR][1000 genomes]
rs17095196	1.00[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17095198	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs17095247	0.93[CHB][hapmap]
rs2658949	0.89[ASN][1000 genomes]
rs2658950	0.86[CHB][hapmap]
rs2658976	0.94[CHB][hapmap]
rs2703049	0.89[ASN][1000 genomes]
rs2703052	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2703056	0.84[ASN][1000 genomes]
rs2703057	0.89[ASN][1000 genomes]
rs2710418	0.87[CHB][hapmap];0.85[JPT][hapmap];0.89[ASN][1000 genomes]
rs2710424	0.94[CHB][hapmap]
rs447760	0.81[CHB][hapmap]
rs57726055	1.00[AMR][1000 genomes]
rs59646766	1.00[AMR][1000 genomes]
rs61438749	0.86[ASN][1000 genomes]
rs71459276	0.86[ASN][1000 genomes]
rs7295338	0.88[CHB][hapmap]
rs7300104	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3378050	chr12:44963059-45264289	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv832394	chr12:45077573-45269305	Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
3	nsv1036926	chr12:45131884-45273648	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
4	nsv541484	chr12:45131884-45273648	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45211600-45227400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:45211800-45224600	Weak transcription	Fetal Intestine Small	intestine
3	chr12:45213600-45237800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:45214000-45224000	Weak transcription	Fetal Brain Female	brain
5	chr12:45219200-45220400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr12:45219400-45221600	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr12:45219600-45221600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr12:45219800-45221400	Enhancers	Primary T cells from cord blood	blood
9	chr12:45220000-45220400	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr12:45220000-45221400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr12:45220200-45220400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr12:45220200-45221400	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr12:45220200-45221400	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr12:45220200-45221600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr12:45220200-45227800	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr12:45220200-45229800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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