Variant report

Variant	rs13156286
Chromosome Location	chr5:94371683-94371684
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10037916	0.81[CHB][hapmap]
rs10463164	0.80[ASN][1000 genomes]
rs10476532	0.86[CHB][hapmap]
rs11135418	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11747168	0.80[ASN][1000 genomes]
rs12652623	0.86[CHB][hapmap]
rs13155160	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13160664	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13163860	0.89[EUR][1000 genomes]
rs13181869	0.81[CHB][hapmap]
rs1426100	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1593464	0.80[JPT][hapmap];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17084368	0.85[CHB][hapmap]
rs2011547	0.88[ASN][1000 genomes]
rs2194946	0.97[ASN][1000 genomes]
rs2347478	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2881646	0.80[CHB][hapmap]
rs4869119	0.95[CHB][hapmap];0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs4869227	1.00[CHB][hapmap];0.89[JPT][hapmap];0.99[ASN][1000 genomes]
rs4869228	1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs4988879	0.95[CHB][hapmap];0.80[JPT][hapmap];0.87[ASN][1000 genomes]
rs6862790	0.85[CHB][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs735989	0.90[CHB][hapmap]
rs737002	0.86[CHB][hapmap]
rs7728007	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7729095	0.90[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs7730096	0.90[CHB][hapmap]
rs929989	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2756469	chr5:94323268-94400017	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94349000-94377800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:94366400-94371800	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr5:94366400-94374200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr5:94369400-94378200	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr5:94369600-94373000	Weak transcription	HUVEC	blood vessel
6	chr5:94371000-94372800	Enhancers	Muscle Satellite Cultured Cells	--
7	chr5:94371600-94371800	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr5:94371600-94372000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr5:94371600-94372200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:94371600-94372800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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