Variant report

Variant	rs2718982
Chromosome Location	chr8:85704370-85704371
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10093758	0.85[EUR][1000 genomes]
rs10105150	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11989750	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11989787	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1488701	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1565225	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2465975	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2465976	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2465977	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2465978	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2465979	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2465980	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2467210	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2467211	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2634042	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2634043	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2634044	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2634045	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2634046	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2634047	0.93[EUR][1000 genomes]
rs2634048	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2634049	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2634050	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2634051	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2634052	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2634053	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2634054	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2634055	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2634056	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2634057	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2634058	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2634059	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2634062	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2634063	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2634064	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2634065	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2634066	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2634067	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2634068	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2634069	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2718963	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2718964	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2718965	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2718967	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2718968	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2718969	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2718970	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2718971	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2718972	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2718973	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2718974	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2718975	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2718977	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2718978	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2718979	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2718980	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2718981	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2718984	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2718985	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2718987	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28405987	0.86[EUR][1000 genomes]
rs60441607	0.80[EUR][1000 genomes]
rs67135531	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6998597	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7820496	0.89[EUR][1000 genomes]
rs901918	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs957815	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs957816	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3481417	chr8:85279453-86145229	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	esv3481418	chr8:85279453-86145229	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats 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	29 gene(s)	inside rSNPs	diseases
3	nsv427823	chr8:85538522-86009068	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv831376	chr8:85577422-85726311	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv891116	chr8:85660437-85792472	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1033771	chr8:85697942-85720299	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:85704200-85704400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:85704200-85704600	Enhancers	Spleen	Spleen
3	chr8:85704200-85704800	Enhancers	Primary T cells from cord blood	blood

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