Variant report

Variant	rs2736551
Chromosome Location	chr11:5389286-5389287
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5384124..5385767-chr11:5387283..5389565,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10837945	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11037097	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11037120	0.83[CEU][hapmap]
rs12360876	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1473547	0.81[CHB][hapmap];0.89[JPT][hapmap]
rs1532514	0.89[JPT][hapmap]
rs2340327	0.94[JPT][hapmap]
rs2471983	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2471984	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2471991	0.83[CEU][hapmap]
rs2647545	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2647547	0.94[JPT][hapmap]
rs2647548	0.95[JPT][hapmap]
rs2647550	0.95[JPT][hapmap]
rs2647551	0.95[JPT][hapmap]
rs2647552	0.95[JPT][hapmap]
rs2647555	0.95[JPT][hapmap]
rs2647556	0.95[JPT][hapmap]
rs2647579	0.83[CEU][hapmap]
rs2647611	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2723375	0.95[JPT][hapmap]
rs2736537	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2736538	0.95[JPT][hapmap]
rs2736539	0.95[JPT][hapmap]
rs2736540	0.95[JPT][hapmap]
rs2736541	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2736544	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2736546	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2736549	0.85[CEU][hapmap];0.81[JPT][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4301813	1.00[CEU][hapmap];0.84[JPT][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4494328	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6421052	0.85[JPT][hapmap]
rs7479727	0.95[JPT][hapmap]
rs951747	0.94[JPT][hapmap]
rs9734220	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv524400	chr11:5328361-5416622	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
2	nsv1048608	chr11:5328516-5645179	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	60 gene(s)	inside rSNPs	diseases
3	nsv1046068	chr11:5335943-6063742	Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
4	nsv896931	chr11:5357881-5505149	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
5	nsv832057	chr11:5375585-5576200	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
6	nsv983147	chr11:5376861-5392760	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5384200-5391200	Enhancers	NHLF	lung
2	chr11:5384200-5391200	Enhancers	Osteobl	bone
3	chr11:5384800-5389600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr11:5384800-5389600	Enhancers	HUVEC	blood vessel
5	chr11:5385000-5389600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr11:5385000-5391400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr11:5386000-5391200	Enhancers	NHDF-Ad	bronchial
8	chr11:5387200-5389600	Enhancers	NH-A	brain
9	chr11:5388000-5390200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr11:5388000-5390400	Enhancers	Hela-S3	cervix
11	chr11:5388200-5389400	Enhancers	Ovary	ovary
12	chr11:5388200-5389600	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr11:5388200-5390400	Enhancers	HSMM	muscle
14	chr11:5388400-5389400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr11:5388400-5389400	Weak transcription	K562	blood
16	chr11:5388800-5389400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr11:5389000-5390600	Weak transcription	HSMMtube	muscle
18	chr11:5389200-5389400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links