Variant report

Variant	rs11182801
Chromosome Location	chr12:45427985-45427986
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10880730	0.82[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs11182799	0.82[EUR][1000 genomes]
rs11182800	0.83[GIH][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.82[EUR][1000 genomes]
rs11182810	0.83[ASN][1000 genomes]
rs11182811	0.83[ASN][1000 genomes]
rs1118481	0.95[JPT][hapmap]
rs11830299	0.82[EUR][1000 genomes]
rs12304054	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1495033	0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs1495042	0.82[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs2160987	0.95[MEX][hapmap]
rs2408140	0.81[ASN][1000 genomes]
rs2658950	1.00[CEU][hapmap]
rs2658976	1.00[CEU][hapmap]
rs2710424	1.00[CEU][hapmap]
rs73277027	0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs73277028	0.89[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs978696	0.82[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3351644	chr12:45345597-45529449	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1045857	chr12:45351172-45468784	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv541485	chr12:45351172-45468784	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45424400-45428800	Weak transcription	Brain Substantia Nigra	brain
2	chr12:45425000-45428600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:45426600-45428600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr12:45427600-45428400	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr12:45427800-45428000	Bivalent Enhancer	Fetal Brain Male	brain
6	chr12:45427800-45428400	Enhancers	Brain Hippocampus Middle	brain
7	chr12:45427800-45428600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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