Variant report

Variant	rs9561464
Chromosome Location	chr13:94557028-94557029
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs12583113	0.91[ASN][1000 genomes]
rs1330459	0.82[ASN][1000 genomes]
rs1411502	0.83[ASN][1000 genomes]
rs1411503	0.82[ASN][1000 genomes]
rs17174714	0.88[ASN][1000 genomes]
rs1888228	0.80[ASN][1000 genomes]
rs2892669	0.85[ASN][1000 genomes]
rs3858844	0.85[ASN][1000 genomes]
rs45608931	0.84[ASN][1000 genomes]
rs4773764	0.82[ASN][1000 genomes]
rs61962148	0.84[ASN][1000 genomes]
rs61964364	0.86[ASN][1000 genomes]
rs61964366	0.91[ASN][1000 genomes]
rs713220	0.87[ASN][1000 genomes]
rs7997761	0.96[ASN][1000 genomes]
rs9516291	0.80[ASN][1000 genomes]
rs9516299	0.86[ASN][1000 genomes]
rs9516307	0.91[ASN][1000 genomes]
rs9516309	0.91[ASN][1000 genomes]
rs9524238	0.80[ASN][1000 genomes]
rs9524244	0.84[ASN][1000 genomes]
rs9524248	0.85[ASN][1000 genomes]
rs9524251	0.84[ASN][1000 genomes]
rs9524255	0.87[ASN][1000 genomes]
rs9524267	0.88[ASN][1000 genomes]
rs955129	0.87[ASN][1000 genomes]
rs9556336	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9561455	0.85[ASN][1000 genomes]
rs9561456	0.84[ASN][1000 genomes]
rs9561466	0.99[ASN][1000 genomes]
rs964508	0.80[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	nsv948714	chr13:94100104-94699435	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv933807	chr13:94187158-94845505	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1045230	chr13:94277683-94764671	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv948455	chr13:94451368-94988900	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv916640	chr13:94521959-95101443	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	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	chr13:94556000-94557600	Enhancers	Fetal Stomach	stomach
2	chr13:94557000-94560600	Weak transcription	Ovary	ovary

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