Variant report

Variant	rs10958223
Chromosome Location	chr8:85603351-85603352
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10090567	0.95[EUR][1000 genomes]
rs10095469	0.95[EUR][1000 genomes]
rs10101057	0.95[EUR][1000 genomes]
rs10103811	1.00[YRI][hapmap]
rs10103984	1.00[EUR][1000 genomes]
rs10106490	0.95[EUR][1000 genomes]
rs10106879	0.95[EUR][1000 genomes]
rs10107192	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10108862	0.95[EUR][1000 genomes]
rs10109673	1.00[GIH][hapmap];1.00[TSI][hapmap]
rs10110773	0.95[EUR][1000 genomes]
rs10111461	0.95[EUR][1000 genomes]
rs10504806	1.00[TSI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10958224	0.93[YRI][hapmap]
rs11984578	1.00[TSI][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11985257	1.00[GIH][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11985284	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11988419	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11989935	1.00[GIH][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11994516	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1320767	1.00[TSI][hapmap]
rs1488702	1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16913052	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16913111	1.00[YRI][hapmap]
rs16913135	1.00[YRI][hapmap]
rs2029358	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28377892	0.95[EUR][1000 genomes]
rs28410514	1.00[EUR][1000 genomes]
rs28470202	1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap]
rs28552445	0.95[EUR][1000 genomes]
rs28615259	1.00[EUR][1000 genomes]
rs28620139	1.00[GIH][hapmap];1.00[TSI][hapmap]
rs28682420	0.95[EUR][1000 genomes]
rs28690245	0.95[EUR][1000 genomes]
rs28701915	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28748272	1.00[EUR][1000 genomes]
rs28750120	0.95[EUR][1000 genomes]
rs28753755	1.00[EUR][1000 genomes]
rs28792691	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28838665	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35982821	0.89[EUR][1000 genomes]
rs6992185	1.00[GIH][hapmap]
rs7009141	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73294048	1.00[EUR][1000 genomes]
rs73294082	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73294084	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7820782	0.95[EUR][1000 genomes]
rs7834473	0.95[EUR][1000 genomes]
rs7839325	0.95[EUR][1000 genomes]
rs7844228	0.95[EUR][1000 genomes]
rs9657052	1.00[MEX][hapmap];0.87[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
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