Variant report

Variant	rs2331576
Chromosome Location	chr4:69779114-69779115
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	chr4:69770351..69773308-chr4:69775332..69780038,5	MCF-7	breast:
2	chr4:69778943..69780754-chr4:69782695..69784707,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000272626	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10000481	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10004381	1.00[EUR][1000 genomes]
rs10005280	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10014997	1.00[EUR][1000 genomes]
rs10015332	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10018123	1.00[EUR][1000 genomes]
rs10030582	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10030703	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1020766	0.84[ASN][1000 genomes]
rs10903222	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1117530	1.00[EUR][1000 genomes]
rs1117531	1.00[EUR][1000 genomes]
rs11728297	0.82[ASN][1000 genomes]
rs1303726	1.00[EUR][1000 genomes]
rs13113179	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13148459	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1379814	1.00[EUR][1000 genomes]
rs1379815	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1458239	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1598901	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1902924	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1984569	0.87[AMR][1000 genomes]
rs2018001	0.80[ASN][1000 genomes]
rs2085571	0.87[AMR][1000 genomes]
rs2125306	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2331566	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2331575	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2877423	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3828503	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3966087	1.00[EUR][1000 genomes]
rs4419538	0.80[ASN][1000 genomes]
rs4643882	0.80[ASN][1000 genomes]
rs6812386	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6814321	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6818594	0.82[ASN][1000 genomes]
rs6851476	0.82[ASN][1000 genomes]
rs6858371	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7657317	1.00[EUR][1000 genomes]
rs7659867	0.82[ASN][1000 genomes]
rs7664636	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7672933	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7678708	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7688541	1.00[EUR][1000 genomes]
rs9329038	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005513	chr4:69446718-69890307	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv999654	chr4:69661415-70132110	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	esv3420586	chr4:69680878-70322918	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
4	esv3398036	chr4:69700493-69841391	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1067773	chr4:69718248-70715727	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	esv3468151	chr4:69718675-70322776	Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
7	esv3468153	chr4:69718675-70322776	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
8	nsv436447	chr4:69743339-69851390	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv4372	chr4:69764499-69810115	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69773400-69779200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:69778200-69779600	ZNF genes & repeats	Fetal Intestine Large	intestine

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