Variant report

Variant	rs6765355
Chromosome Location	chr3:115806715-115806716
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs11425708	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11918080	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12695319	0.80[ASN][1000 genomes]
rs13100914	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13315058	0.80[ASN][1000 genomes]
rs1344131	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17630430	0.82[ASN][1000 genomes]
rs17697994	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1920360	0.80[ASN][1000 genomes]
rs1920379	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2091669	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2222827	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2864066	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2864067	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28735793	0.83[ASN][1000 genomes]
rs33956431	0.89[ASN][1000 genomes]
rs34523792	0.82[ASN][1000 genomes]
rs34543919	0.80[ASN][1000 genomes]
rs34844901	0.89[ASN][1000 genomes]
rs34930794	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35080450	0.80[ASN][1000 genomes]
rs35242629	0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35619123	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35780065	0.89[ASN][1000 genomes]
rs35914238	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4263291	0.98[ASN][1000 genomes]
rs4831121	0.80[ASN][1000 genomes]
rs4831225	0.80[ASN][1000 genomes]
rs4831226	0.80[ASN][1000 genomes]
rs4831227	0.89[ASN][1000 genomes]
rs4831228	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4831229	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4831230	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5004406	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56121547	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62269168	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs62269170	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62271281	0.80[ASN][1000 genomes]
rs66490447	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6772113	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73139202	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7632265	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7637650	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9289042	0.88[ASN][1000 genomes]
rs9813038	0.88[ASN][1000 genomes]
rs9816425	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9821040	0.80[ASN][1000 genomes]
rs9821865	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9822568	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9824605	0.80[ASN][1000 genomes]
rs9836963	0.89[ASN][1000 genomes]
rs9837276	0.89[ASN][1000 genomes]
rs9839078	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9851643	0.82[ASN][1000 genomes]
rs9854345	0.89[ASN][1000 genomes]
rs9854711	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9855097	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9857520	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9858539	0.80[ASN][1000 genomes]
rs9866484	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9868706	0.80[ASN][1000 genomes]
rs9873576	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9877662	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9878559	0.80[ASN][1000 genomes]
rs9985471	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760762	chr3:115476222-115807650	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv829685	chr3:115643521-115812913	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv1012260	chr3:115680931-115935968	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2756413	chr3:115721898-115908480	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	esv2751975	chr3:115766285-115902901	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:115780400-115830000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:115801200-115821400	Weak transcription	Fetal Lung	lung
3	chr3:115802000-115807000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:115804600-115821200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr3:115805000-115809200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr3:115806000-115807400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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