Variant report

Variant	rs9483414
Chromosome Location	chr6:132536703-132536704
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	6:132269655-132282174..6:132533382-132536758	H1-hESC	embryonic stem cell:	embryo

Variant related genes	Relation type
ENSG00000118523	Chromatin interaction
ENSG00000227220	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1321261	0.82[CEU][hapmap];0.80[JPT][hapmap]
rs1321278	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1321279	1.00[CEU][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1321280	0.81[CEU][hapmap];0.80[JPT][hapmap]
rs1406935	0.82[CEU][hapmap];0.81[JPT][hapmap]
rs1406939	1.00[CEU][hapmap];0.95[YRI][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1406940	0.96[CEU][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1535196	1.00[CEU][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1535197	0.82[CEU][hapmap];0.85[JPT][hapmap]
rs3927419	0.84[CEU][hapmap];0.84[JPT][hapmap]
rs4142807	1.00[CEU][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4142808	1.00[CEU][hapmap];0.95[JPT][hapmap];0.87[YRI][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6569777	1.00[CEU][hapmap];0.95[JPT][hapmap];0.91[YRI][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6935755	0.81[CEU][hapmap]
rs7739344	0.82[CEU][hapmap];0.81[JPT][hapmap]
rs7739499	0.81[CEU][hapmap]
rs7742430	1.00[CEU][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7760956	0.96[CEU][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7761388	0.88[JPT][hapmap];0.86[YRI][hapmap];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9375866	0.82[CEU][hapmap];0.80[JPT][hapmap]
rs9385597	0.81[CEU][hapmap]
rs9388967	0.81[JPT][hapmap]
rs9402390	1.00[CEU][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9402391	0.82[CEU][hapmap];0.80[JPT][hapmap]
rs9493239	1.00[CEU][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9493240	0.81[CEU][hapmap];0.85[JPT][hapmap]

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	esv2762616	chr6:132404708-132584324	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1024527	chr6:132532941-132571889	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132532200-132537200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr6:132532600-132537200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:132536000-132537600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:132536200-132537000	Weak transcription	Aorta	Aorta
5	chr6:132536200-132537200	Weak transcription	Pancreas	Pancrea

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