Variant report

Variant	rs3853208
Chromosome Location	chr5:95834459-95834460
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAST-7	chr5:95834419-95835762	NONHSAT102893

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10515238	1.00[ASN][1000 genomes]
rs11135464	1.00[ASN][1000 genomes]
rs11135465	1.00[ASN][1000 genomes]
rs11739740	1.00[ASN][1000 genomes]
rs11744768	1.00[ASN][1000 genomes]
rs12516760	1.00[ASN][1000 genomes]
rs12517435	1.00[ASN][1000 genomes]
rs12519934	1.00[ASN][1000 genomes]
rs1560837	1.00[ASN][1000 genomes]
rs1560838	1.00[ASN][1000 genomes]
rs1566338	1.00[ASN][1000 genomes]
rs17394413	1.00[ASN][1000 genomes]
rs17473246	1.00[ASN][1000 genomes]
rs17473575	1.00[ASN][1000 genomes]
rs183784	1.00[ASN][1000 genomes]
rs187771	1.00[ASN][1000 genomes]
rs261224	1.00[ASN][1000 genomes]
rs261228	1.00[ASN][1000 genomes]
rs261239	1.00[ASN][1000 genomes]
rs261241	1.00[ASN][1000 genomes]
rs263376	1.00[ASN][1000 genomes]
rs35335212	1.00[ASN][1000 genomes]
rs35758052	1.00[ASN][1000 genomes]
rs3853209	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3866380	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55668618	1.00[ASN][1000 genomes]
rs56188323	1.00[ASN][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	nsv1030444	chr5:95353620-95995619	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv537810	chr5:95353620-95995619	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1024964	chr5:95742124-96065492	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv537811	chr5:95742124-96065492	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
5	nsv1026484	chr5:95759910-95961518	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:95812600-95840400	Weak transcription	Aorta	Aorta
2	chr5:95834200-95836800	Enhancers	Hela-S3	cervix

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