Variant report

Variant	rs4258914
Chromosome Location	chr3:157199001-157199002
allele	A/C
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:27)

rs_ID	r²[population]
rs1011060	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10513515	0.96[YRI][hapmap]
rs12635273	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1350149	0.86[CHB][hapmap];0.81[ASN][1000 genomes]
rs16827705	0.87[YRI][hapmap]
rs16827727	0.96[YRI][hapmap];0.80[AFR][1000 genomes]
rs2165873	0.91[CHB][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs2316337	0.81[ASN][1000 genomes]
rs4611770	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4679796	0.96[CEU][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4680371	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs4680372	0.86[CHB][hapmap]
rs62280977	0.81[ASN][1000 genomes]
rs62280978	0.80[ASN][1000 genomes]
rs62280979	0.81[ASN][1000 genomes]
rs62280980	0.81[ASN][1000 genomes]
rs62280981	0.81[ASN][1000 genomes]
rs62280982	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6441133	0.81[CHB][hapmap]
rs67118252	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs67228252	0.81[ASN][1000 genomes]
rs6779693	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73158523	0.80[AFR][1000 genomes]
rs73158525	0.80[AFR][1000 genomes]
rs73158530	0.81[ASN][1000 genomes]
rs9682174	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs988757	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[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	esv2757900	chr3:157090166-157254684	Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv2759193	chr3:157090166-157254684	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:157185600-157211400	Weak transcription	HSMM	muscle
2	chr3:157187600-157210600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr3:157188000-157203000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr3:157189400-157199400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr3:157194000-157212000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:157194400-157210200	Weak transcription	NH-A	brain
7	chr3:157194600-157217000	Weak transcription	Pancreas	Pancrea
8	chr3:157194800-157212000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr3:157198800-157200000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr3:157198800-157204400	Weak transcription	HUVEC	blood vessel
11	chr3:157198800-157210400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:157199000-157200400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr3:157199000-157200600	Weak transcription	Osteobl	bone
14	chr3:157199000-157211600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links