Variant report

Variant	rs1359214
Chromosome Location	chr13:37876982-37876983
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1006078	0.87[ASN][1000 genomes]
rs12583265	0.91[ASN][1000 genomes]
rs1324024	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1324025	0.99[ASN][1000 genomes]
rs1324038	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1359215	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17226415	0.82[ASN][1000 genomes]
rs1853577	0.97[ASN][1000 genomes]
rs1951902	0.82[ASN][1000 genomes]
rs1998565	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1998566	0.99[ASN][1000 genomes]
rs2147177	0.87[ASN][1000 genomes]
rs2224848	0.99[ASN][1000 genomes]
rs4941860	0.87[ASN][1000 genomes]
rs58106020	0.87[ASN][1000 genomes]
rs59032957	0.81[ASN][1000 genomes]
rs61637674	0.87[ASN][1000 genomes]
rs61947165	0.87[ASN][1000 genomes]
rs61947173	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6563526	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7489943	0.87[ASN][1000 genomes]
rs9547775	0.89[ASN][1000 genomes]
rs9566205	0.80[ASN][1000 genomes]
rs9566208	0.89[ASN][1000 genomes]
rs9566210	0.89[ASN][1000 genomes]
rs9576232	0.80[ASN][1000 genomes]
rs9576233	0.82[ASN][1000 genomes]
rs9576235	0.82[ASN][1000 genomes]
rs9576236	0.82[ASN][1000 genomes]
rs9576239	0.88[ASN][1000 genomes]
rs9576240	0.88[ASN][1000 genomes]
rs9576242	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948975	chr13:37281203-38280430	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv899994	chr13:37816086-38087145	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1038850	chr13:37820489-38209571	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv471128	chr13:37838294-37880725	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv34109	chr13:37843819-38276391	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 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	chr13:37861400-37877200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr13:37876800-37877000	Enhancers	Muscle Satellite Cultured Cells	--

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