Variant report

Variant	rs9534589
Chromosome Location	chr13:47872698-47872699
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12561429	0.92[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs6561367	0.82[JPT][hapmap]
rs6561368	0.98[ASN][1000 genomes]
rs7329520	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7999656	0.86[CEU][hapmap];0.83[JPT][hapmap]
rs9526300	0.87[ASN][1000 genomes]
rs9526301	0.87[ASN][1000 genomes]
rs9526305	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9526307	0.82[CEU][hapmap];0.82[JPT][hapmap];0.85[EUR][1000 genomes]
rs9526312	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9526313	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs9526315	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9534584	0.83[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs9534590	0.97[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs9534593	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs9567823	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2763019	chr13:47348229-48123447	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv3394678	chr13:47678184-48039379	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv832599	chr13:47703075-47873855	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:47862800-47874200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr13:47872600-47873200	Enhancers	HMEC	breast
3	chr13:47872600-47873400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr13:47872600-47873400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr13:47872600-47874400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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