Variant report

Variant	rs613548
Chromosome Location	chr11:59990712-59990713
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1426252	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2081546	0.96[ASN][1000 genomes]
rs2243987	0.84[ASN][1000 genomes]
rs2433240	0.84[ASN][1000 genomes]
rs581818	0.84[ASN][1000 genomes]
rs582407	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs585540	0.84[AFR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs587634	0.84[ASN][1000 genomes]
rs590351	0.82[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs590532	0.82[ASN][1000 genomes]
rs592496	0.84[ASN][1000 genomes]
rs594414	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs595014	0.84[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs596788	0.84[ASN][1000 genomes]
rs598862	0.84[ASN][1000 genomes]
rs605820	0.82[ASN][1000 genomes]
rs607639	0.86[AFR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs613629	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs615405	0.86[AFR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs624233	0.84[ASN][1000 genomes]
rs625025	0.84[ASN][1000 genomes]
rs636988	0.86[AFR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs638872	0.84[ASN][1000 genomes]
rs641051	0.84[ASN][1000 genomes]
rs641829	0.84[AFR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs642426	0.84[ASN][1000 genomes]
rs646924	0.84[ASN][1000 genomes]
rs649234	0.84[AFR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs650777	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs650853	0.86[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs650926	0.86[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs653285	0.84[ASN][1000 genomes]
rs654443	0.84[ASN][1000 genomes]
rs661376	0.84[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs662674	0.84[AFR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs668095	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs668134	0.84[AFR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs670925	0.84[ASN][1000 genomes]
rs672218	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs674971	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs675316	0.83[ASN][1000 genomes]
rs675452	0.93[ASN][1000 genomes]
rs680699	0.82[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs682739	0.84[ASN][1000 genomes]
rs684977	0.84[ASN][1000 genomes]
rs73485360	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832174	chr11:59909267-60073908	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1053558	chr11:59979460-60061209	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 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	chr11:59989400-59991200	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr11:59989600-59992200	Strong transcription	Primary monocytes fromperipheralblood	blood

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