Variant report

Variant	rs11182637
Chromosome Location	chr12:45146682-45146683
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10880664	0.95[ASN][1000 genomes]
rs11182619	0.86[ASN][1000 genomes]
rs11182620	0.86[ASN][1000 genomes]
rs11182623	0.95[ASN][1000 genomes]
rs11182624	0.95[ASN][1000 genomes]
rs11182625	0.91[ASN][1000 genomes]
rs11182626	0.91[ASN][1000 genomes]
rs11182629	0.95[ASN][1000 genomes]
rs11182632	0.95[ASN][1000 genomes]
rs11182638	1.00[ASN][1000 genomes]
rs11182641	0.91[ASN][1000 genomes]
rs11182642	1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11182643	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182644	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182645	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182646	1.00[ASN][1000 genomes]
rs11182648	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182649	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182650	1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11182651	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182652	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182653	0.95[ASN][1000 genomes]
rs12227809	0.81[ASN][1000 genomes]
rs17094775	1.00[AMR][1000 genomes]
rs17094809	1.00[AMR][1000 genomes]
rs17094817	1.00[AMR][1000 genomes]
rs17094822	1.00[AMR][1000 genomes]
rs17094832	1.00[AMR][1000 genomes]
rs17094847	1.00[AMR][1000 genomes]
rs17094988	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17595910	1.00[AMR][1000 genomes]
rs7965452	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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	nsv1049080	chr12:45097564-45195295	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
4	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
5	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:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45134400-45165200	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr12:45135400-45175000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:45145000-45150200	Weak transcription	Fetal Brain Male	brain
4	chr12:45145000-45150600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:45145000-45172200	Weak transcription	Fetal Brain Female	brain
6	chr12:45145200-45169600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr12:45146000-45147200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr12:45146200-45147200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:45146400-45147000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr12:45146600-45146800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:45146600-45146800	Enhancers	Primary T helper cells PMA-I stimulated	--

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