Variant report

Variant	rs4130781
Chromosome Location	chr2:212594948-212594949
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:212593545..212595397-chr2:212598538..212601478,2	MCF-7	breast:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs12620444	1.00[CHB][hapmap]
rs12620559	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12622176	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13035133	1.00[CHB][hapmap]
rs35444377	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4130782	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4132462	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55758468	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55769536	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55897719	0.94[EUR][1000 genomes]
rs56405287	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61079605	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62182986	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62182989	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62182991	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62182999	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62183021	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62183023	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62183024	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62183028	0.95[ASN][1000 genomes]
rs62183029	0.95[ASN][1000 genomes]
rs62183031	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6749448	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6756725	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs72946582	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72948506	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7422793	0.88[CEU][hapmap];0.88[EUR][1000 genomes]
rs7556896	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7564414	1.00[JPT][hapmap]
rs7600261	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs7601502	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34128	chr2:212581485-212857122	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212583600-212595400	Weak transcription	Brain Anterior Caudate	brain
2	chr2:212587400-212595000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:212594400-212595000	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr2:212594400-212595200	Enhancers	Brain Substantia Nigra	brain
5	chr2:212594800-212595200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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