Variant report

Variant	rs6586879
Chromosome Location	chr8:19762732-19762733
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10092137	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10092531	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10092538	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10099404	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10102021	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10102032	0.91[EUR][1000 genomes]
rs10102045	1.00[EUR][1000 genomes]
rs10102876	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs10107119	1.00[EUR][1000 genomes]
rs10111437	1.00[EUR][1000 genomes]
rs1031045	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs10503667	1.00[EUR][1000 genomes]
rs11992664	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11997573	1.00[EUR][1000 genomes]
rs1470186	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs17091738	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17091742	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs17482338	1.00[EUR][1000 genomes]
rs1800590	1.00[CEU][hapmap];0.92[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1801177	1.00[EUR][1000 genomes]
rs2410615	0.91[EUR][1000 genomes]
rs28371439	1.00[EUR][1000 genomes]
rs28445964	1.00[EUR][1000 genomes]
rs28522139	1.00[EUR][1000 genomes]
rs28568947	1.00[EUR][1000 genomes]
rs28575919	1.00[EUR][1000 genomes]
rs28582042	1.00[EUR][1000 genomes]
rs28615996	1.00[EUR][1000 genomes]
rs28645722	1.00[EUR][1000 genomes]
rs28689946	1.00[EUR][1000 genomes]
rs28786747	1.00[EUR][1000 genomes]
rs35469180	0.91[EUR][1000 genomes]
rs3854905	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3900537	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3951339	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4368997	1.00[EUR][1000 genomes]
rs56043715	1.00[EUR][1000 genomes]
rs59811201	1.00[EUR][1000 genomes]
rs60633545	1.00[EUR][1000 genomes]
rs60901125	1.00[EUR][1000 genomes]
rs6984990	1.00[EUR][1000 genomes]
rs6995406	1.00[EUR][1000 genomes]
rs6996383	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6997330	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6998260	1.00[EUR][1000 genomes]
rs6999612	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7000460	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs7008626	0.91[EUR][1000 genomes]
rs7009128	0.83[EUR][1000 genomes]
rs7016529	1.00[EUR][1000 genomes]
rs73667455	1.00[EUR][1000 genomes]
rs73667459	1.00[EUR][1000 genomes]
rs73667461	1.00[EUR][1000 genomes]
rs73667462	1.00[EUR][1000 genomes]
rs73667463	1.00[EUR][1000 genomes]
rs73667465	1.00[EUR][1000 genomes]
rs73667468	1.00[EUR][1000 genomes]
rs73667469	1.00[EUR][1000 genomes]
rs73667470	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7818864	1.00[EUR][1000 genomes]
rs7835874	1.00[EUR][1000 genomes]
rs7840666	1.00[EUR][1000 genomes]
rs7840815	1.00[EUR][1000 genomes]
rs7840959	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890625	chr8:19368697-19799641	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv610759	chr8:19561997-20068842	Enhancers Strong transcription Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv498082	chr8:19722435-19873112	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	esv32767	chr8:19740189-19873082	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	nsv1033511	chr8:19751299-20625091	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19761800-19763600	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr8:19761800-19764400	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr8:19762600-19763200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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