Variant report

Variant	rs2903765
Chromosome Location	chr4:82311291-82311292
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10013788	0.93[ASN][1000 genomes]
rs10017744	0.84[EUR][1000 genomes]
rs10028610	0.93[ASN][1000 genomes]
rs10488932	0.88[AFR][1000 genomes]
rs11727754	0.84[EUR][1000 genomes]
rs11731567	0.85[EUR][1000 genomes]
rs11732106	0.93[ASN][1000 genomes]
rs11736471	0.93[ASN][1000 genomes]
rs11736583	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11939135	0.85[EUR][1000 genomes]
rs12332030	0.99[ASN][1000 genomes]
rs13435660	0.85[EUR][1000 genomes]
rs1377055	0.80[AFR][1000 genomes]
rs1452367	0.82[EUR][1000 genomes]
rs1551236	0.95[ASN][1000 genomes]
rs17428097	0.99[ASN][1000 genomes]
rs17428153	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17500037	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17500100	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1993160	0.85[EUR][1000 genomes]
rs2041461	0.86[EUR][1000 genomes]
rs2058367	0.85[EUR][1000 genomes]
rs2159656	0.83[EUR][1000 genomes]
rs59493042	0.81[EUR][1000 genomes]
rs62303573	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6535243	0.84[EUR][1000 genomes]
rs6814785	0.84[EUR][1000 genomes]
rs6819909	0.84[EUR][1000 genomes]
rs6839968	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs6851443	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7654102	0.85[EUR][1000 genomes]
rs7660089	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7664953	0.85[EUR][1000 genomes]
rs7669131	0.85[EUR][1000 genomes]
rs7673578	0.85[EUR][1000 genomes]
rs7677239	0.85[EUR][1000 genomes]
rs7681976	0.80[EUR][1000 genomes]
rs9307782	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]

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	nsv999729	chr4:81802554-82627820	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537156	chr4:81802554-82627820	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv829985	chr4:82199328-82353656	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv980406	chr4:82310479-82337709	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:82310200-82311600	Enhancers	Primary monocytes fromperipheralblood	blood

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