Variant report

Variant	rs167505
Chromosome Location	chr4:127553424-127553425
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10005082	0.95[ASN][1000 genomes]
rs1160368	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11937789	0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs13134248	0.93[ASN][1000 genomes]
rs1511140	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1552665	0.87[ASN][1000 genomes]
rs167504	0.82[ASN][1000 genomes]
rs17011443	0.83[ASN][1000 genomes]
rs170195	0.82[ASN][1000 genomes]
rs170196	0.86[ASN][1000 genomes]
rs17200542	0.94[ASN][1000 genomes]
rs178299	0.82[ASN][1000 genomes]
rs186366	0.81[ASN][1000 genomes]
rs2391077	0.88[ASN][1000 genomes]
rs313046	0.82[ASN][1000 genomes]
rs313047	0.82[ASN][1000 genomes]
rs313048	0.82[ASN][1000 genomes]
rs313049	0.80[ASN][1000 genomes]
rs313050	0.82[ASN][1000 genomes]
rs313063	0.82[ASN][1000 genomes]
rs313066	0.82[ASN][1000 genomes]
rs313067	0.82[ASN][1000 genomes]
rs313069	0.86[ASN][1000 genomes]
rs313070	0.86[ASN][1000 genomes]
rs313071	0.86[ASN][1000 genomes]
rs313072	0.86[ASN][1000 genomes]
rs313099	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs313124	0.88[JPT][hapmap]
rs434002	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs435220	0.86[ASN][1000 genomes]
rs447507	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4833351	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62324174	0.83[ASN][1000 genomes]
rs6857039	0.86[ASN][1000 genomes]
rs7691175	0.87[JPT][hapmap];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012833	chr4:127468474-127760933	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv537242	chr4:127468474-127760933	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv524850	chr4:127470903-127768849	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1013854	chr4:127508969-127663216	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1009499	chr4:127532856-127659010	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv537243	chr4:127532856-127659010	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127552200-127557400	Weak transcription	Gastric	stomach
2	chr4:127553000-127554400	Strong transcription	K562	blood

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