Variant report

Variant	rs7818433
Chromosome Location	chr8:91146725-91146726
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:91142074..91143853-chr8:91145432..91147703,2	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10504888	1.00[JPT][hapmap]
rs10504891	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12675530	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13312921	0.92[JPT][hapmap]
rs13312954	0.92[JPT][hapmap]
rs16901941	0.92[JPT][hapmap]
rs16902273	1.00[JPT][hapmap]
rs16902355	1.00[JPT][hapmap]
rs16902558	1.00[JPT][hapmap]
rs16903927	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16904011	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16904073	1.00[CEU][hapmap]
rs1805811	0.92[JPT][hapmap]
rs1805824	0.92[JPT][hapmap]
rs1805826	0.92[JPT][hapmap]
rs1805837	0.92[JPT][hapmap]
rs1805855	1.00[JPT][hapmap]
rs1805862	1.00[JPT][hapmap]
rs1805880	1.00[JPT][hapmap]
rs1805882	1.00[JPT][hapmap]
rs1805885	1.00[JPT][hapmap]
rs1805888	1.00[JPT][hapmap]
rs1805892	0.83[ASN][1000 genomes]
rs1805894	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs1805901	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1805902	1.00[CEU][hapmap];0.86[CHB][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs1805907	1.00[CEU][hapmap];0.86[CHB][hapmap];0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs1805911	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs1805912	1.00[CEU][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs1805914	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs1805915	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2074594	1.00[JPT][hapmap]
rs2074595	1.00[JPT][hapmap]
rs2280779	0.92[JPT][hapmap]
rs3026287	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs3358	0.92[JPT][hapmap]
rs3758145	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6982611	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6997558	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7001425	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs769418	0.92[JPT][hapmap]
rs7813378	1.00[JPT][hapmap]
rs7818138	0.92[JPT][hapmap]
rs7822786	1.00[JPT][hapmap]
rs7826471	1.00[JPT][hapmap]
rs7836381	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7844005	1.00[JPT][hapmap]
rs7845155	1.00[JPT][hapmap]
rs7845669	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758164	chr8:91000786-91329669	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv2759628	chr8:91000786-91329669	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	esv2757281	chr8:91090821-91235335	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	esv34347	chr8:91101339-91179126	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
5	nsv470225	chr8:91113616-91229254	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
6	nsv891184	chr8:91114698-91222654	Active TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
7	nsv824687	chr8:91144854-91177488	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	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	chr8:91141600-91150400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:91145800-91146800	Enhancers	K562	blood

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