Variant report

Variant	rs57058080
Chromosome Location	chr9:84846057-84846058
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10117890	0.86[ASN][1000 genomes]
rs10123309	0.86[ASN][1000 genomes]
rs10780541	0.96[ASN][1000 genomes]
rs10867832	0.96[ASN][1000 genomes]
rs10867834	0.96[ASN][1000 genomes]
rs10867835	0.91[ASN][1000 genomes]
rs10867836	0.88[ASN][1000 genomes]
rs10867837	0.87[ASN][1000 genomes]
rs10867839	0.85[ASN][1000 genomes]
rs10867840	0.83[ASN][1000 genomes]
rs11139538	0.83[ASN][1000 genomes]
rs11794308	0.84[ASN][1000 genomes]
rs1200755	0.89[ASN][1000 genomes]
rs1209749	0.82[ASN][1000 genomes]
rs1327254	0.91[ASN][1000 genomes]
rs1330834	0.83[ASN][1000 genomes]
rs1411668	0.81[ASN][1000 genomes]
rs1890344	0.86[ASN][1000 genomes]
rs1933577	0.85[ASN][1000 genomes]
rs1933580	0.81[ASN][1000 genomes]
rs1933583	0.80[ASN][1000 genomes]
rs1933584	0.83[ASN][1000 genomes]
rs1933586	0.83[ASN][1000 genomes]
rs2038995	0.89[ASN][1000 genomes]
rs2767709	0.89[ASN][1000 genomes]
rs2767711	0.86[ASN][1000 genomes]
rs2788106	0.82[ASN][1000 genomes]
rs2788107	0.81[ASN][1000 genomes]
rs2788110	0.80[ASN][1000 genomes]
rs2788114	0.83[ASN][1000 genomes]
rs2788115	0.86[ASN][1000 genomes]
rs2993516	0.83[ASN][1000 genomes]
rs4263847	0.84[ASN][1000 genomes]
rs4276765	0.80[ASN][1000 genomes]
rs4338186	0.81[ASN][1000 genomes]
rs4489388	0.95[ASN][1000 genomes]
rs4563967	0.85[ASN][1000 genomes]
rs4877229	0.83[ASN][1000 genomes]
rs4877691	0.81[ASN][1000 genomes]
rs6559656	0.88[ASN][1000 genomes]
rs7021352	0.84[ASN][1000 genomes]
rs7025964	0.94[ASN][1000 genomes]
rs7027988	0.94[ASN][1000 genomes]
rs7848262	0.81[ASN][1000 genomes]
rs7852603	0.81[ASN][1000 genomes]
rs7857885	0.85[ASN][1000 genomes]
rs7859164	0.84[ASN][1000 genomes]
rs7859493	0.84[ASN][1000 genomes]
rs7861490	0.96[ASN][1000 genomes]
rs986510	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049305	chr9:84667596-84918690	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv831640	chr9:84695958-84880535	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv893507	chr9:84799537-85097651	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr9:84845800-84846400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:84846000-84846600	Enhancers	Colonic Mucosa	Colon

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