Variant report

Variant	rs7665257
Chromosome Location	chr4:19732458-19732459
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10516335	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11721854	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11721864	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11722812	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11930962	1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11936583	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11939339	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11942433	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17511289	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17511324	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17511721	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17570085	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17570168	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs28629819	0.94[EUR][1000 genomes]
rs4130540	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs56182249	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62295090	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62295099	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62295100	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62295102	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62295104	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62295107	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62295108	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62295139	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62295153	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62296261	0.94[EUR][1000 genomes]
rs62296262	0.94[EUR][1000 genomes]
rs62296264	0.94[EUR][1000 genomes]
rs62296266	0.94[EUR][1000 genomes]
rs62296271	0.94[EUR][1000 genomes]
rs62296870	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs62296887	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62296905	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6848523	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6853029	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73236204	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73803154	0.81[AFR][1000 genomes]
rs73803156	0.82[AFR][1000 genomes]
rs7667493	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7675318	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs901927	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][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	nsv878733	chr4:19335464-19928602	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv829873	chr4:19582263-19742515	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv829874	chr4:19635213-19781102	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv529290	chr4:19658583-20173839	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	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	chr4:19730800-19732800	Enhancers	Primary hematopoietic stem cells	blood
2	chr4:19731400-19732600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:19731400-19732800	Flanking Active TSS	Dnd41	blood
4	chr4:19731600-19732600	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr4:19732200-19733400	Enhancers	Primary B cells from cord blood	blood
6	chr4:19732400-19732800	Enhancers	HUVEC	blood vessel
7	chr4:19732400-19736400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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