Variant report

Variant	rs341316
Chromosome Location	chr5:111829027-111829028
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:111827330..111830310-chr5:111838037..111840196,2	MCF-7	breast:
2	chr5:111754059..111755568-chr5:111828134..111829745,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000268358	Chromatin interaction
ENSG00000129595	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10037635	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10043247	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10043303	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10043305	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10463632	0.82[ASN][1000 genomes]
rs10463633	0.81[ASN][1000 genomes]
rs10463635	0.81[ASN][1000 genomes]
rs10478092	0.84[ASN][1000 genomes]
rs11748606	0.83[ASN][1000 genomes]
rs11749490	0.84[ASN][1000 genomes]
rs11958362	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs168182	0.81[ASN][1000 genomes]
rs255702	0.84[ASN][1000 genomes]
rs341309	0.81[ASN][1000 genomes]
rs341310	0.81[ASN][1000 genomes]
rs341311	0.81[ASN][1000 genomes]
rs341314	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs341317	0.81[ASN][1000 genomes]
rs341318	0.81[ASN][1000 genomes]
rs341319	1.00[ASN][1000 genomes]
rs341320	0.81[ASN][1000 genomes]
rs341321	0.81[ASN][1000 genomes]
rs341322	0.81[ASN][1000 genomes]
rs341323	0.81[ASN][1000 genomes]
rs341328	1.00[ASN][1000 genomes]
rs341329	1.00[ASN][1000 genomes]
rs341330	1.00[ASN][1000 genomes]
rs341331	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs456145	0.81[ASN][1000 genomes]
rs456305	0.81[ASN][1000 genomes]
rs456491	0.98[ASN][1000 genomes]
rs458204	0.81[ASN][1000 genomes]
rs459290	0.81[ASN][1000 genomes]
rs459306	0.82[ASN][1000 genomes]
rs459369	0.81[ASN][1000 genomes]
rs463532	1.00[ASN][1000 genomes]
rs463588	0.81[ASN][1000 genomes]
rs464453	0.81[ASN][1000 genomes]
rs465021	0.81[ASN][1000 genomes]
rs465644	1.00[ASN][1000 genomes]
rs55713401	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55818114	0.86[AFR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56019374	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57909030	0.82[EUR][1000 genomes]
rs58170444	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72789912	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72789914	0.82[EUR][1000 genomes];0.82[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	nsv599368	chr5:111399885-112032675	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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