Variant report

Variant	rs7805623
Chromosome Location	chr7:39356882-39356883
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:39356708..39357326-chr7:39504458..39505136,2	MCF-7	breast:
2	chr7:39351047..39353326-chr7:39354900..39357326,2	K562	blood:

Variant related genes	Relation type
ENSG00000106536	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10447663	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10447664	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12666828	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12671242	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34905355	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35354413	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4236357	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4256493	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4338004	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs4364548	0.81[CEU][hapmap];0.85[CHB][hapmap]
rs4628166	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs4720318	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4720319	0.96[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4723851	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4723852	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4723854	1.00[CEU][hapmap];0.86[CHB][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4723855	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4723856	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4723857	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60467141	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6462902	1.00[CEU][hapmap]
rs6462905	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6462907	1.00[CEU][hapmap];0.85[CHB][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6462908	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6462909	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6951119	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6962816	1.00[CEU][hapmap];0.85[CHB][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6971051	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7806341	1.00[CEU][hapmap];0.85[CHB][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7806608	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]

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	nsv1015572	chr7:39185895-39413053	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv538821	chr7:39185895-39413053	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv887969	chr7:39265429-39391875	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39350600-39358400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:39354800-39358800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:39355200-39357600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr7:39355400-39359000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:39355800-39358400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:39356400-39357000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:39356600-39357000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr7:39356800-39357000	Enhancers	H1 Cell Line	embryonic stem cell

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