Variant report

Variant	rs7712165
Chromosome Location	chr5:116625850-116625851
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10035146	0.84[EUR][1000 genomes]
rs10037418	0.84[EUR][1000 genomes]
rs10066055	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10068349	0.81[AFR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10068673	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10079309	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10080021	0.85[EUR][1000 genomes]
rs10085046	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10463690	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10478339	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11241420	0.81[ASN][1000 genomes]
rs11957082	0.85[EUR][1000 genomes]
rs12652528	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13170803	0.88[EUR][1000 genomes]
rs13184380	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1353285	0.84[EUR][1000 genomes]
rs1389934	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1389935	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1494818	0.83[EUR][1000 genomes]
rs1494820	0.87[EUR][1000 genomes]
rs1494821	0.89[EUR][1000 genomes]
rs1494823	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1565889	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1565890	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1565892	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1908408	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1908409	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1976282	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2036024	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2220858	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2900101	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34469130	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35793287	0.84[EUR][1000 genomes]
rs4331937	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4435900	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4642406	0.86[EUR][1000 genomes]
rs55813945	0.85[EUR][1000 genomes]
rs56020309	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs60269947	0.86[EUR][1000 genomes]
rs6595020	0.85[EUR][1000 genomes]
rs6595026	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6595028	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6862441	0.84[EUR][1000 genomes]
rs7702997	0.85[EUR][1000 genomes]
rs7703434	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7714476	0.85[EUR][1000 genomes]
rs7729749	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7730432	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7732328	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7735145	0.87[ASN][1000 genomes]
rs7735868	0.87[ASN][1000 genomes]
rs7736463	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015741	chr5:116525936-116665270	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv599486	chr5:116607979-116669707	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116625800-116626400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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