Variant report

Variant	rs57805650
Chromosome Location	chr1:45651118-45651119
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1152028	0.84[ASN][1000 genomes]
rs1226732	0.84[ASN][1000 genomes]
rs1226750	0.84[ASN][1000 genomes]
rs1612575	0.84[ASN][1000 genomes]
rs173208	0.84[ASN][1000 genomes]
rs1969084	0.84[ASN][1000 genomes]
rs1995403	0.84[ASN][1000 genomes]
rs2105460	0.82[ASN][1000 genomes]
rs346685	0.84[ASN][1000 genomes]
rs346686	0.82[ASN][1000 genomes]
rs346688	0.84[ASN][1000 genomes]
rs346689	0.84[ASN][1000 genomes]
rs346692	0.84[ASN][1000 genomes]
rs346703	0.84[ASN][1000 genomes]
rs346704	0.84[ASN][1000 genomes]
rs346709	0.84[ASN][1000 genomes]
rs346710	0.86[ASN][1000 genomes]
rs346711	0.84[ASN][1000 genomes]
rs346718	0.84[ASN][1000 genomes]
rs346720	0.84[ASN][1000 genomes]
rs346725	0.84[ASN][1000 genomes]
rs346726	0.84[ASN][1000 genomes]
rs346730	0.84[ASN][1000 genomes]
rs409082	0.84[ASN][1000 genomes]
rs412055	0.84[ASN][1000 genomes]
rs4415614	0.84[ASN][1000 genomes]
rs4660835	0.80[ASN][1000 genomes]
rs55826381	0.88[ASN][1000 genomes]
rs55842174	0.84[ASN][1000 genomes]
rs55884892	0.88[ASN][1000 genomes]
rs61574129	0.82[ASN][1000 genomes]
rs72684447	0.84[ASN][1000 genomes]
rs72684454	0.84[ASN][1000 genomes]
rs72684481	0.84[ASN][1000 genomes]
rs72684482	0.84[ASN][1000 genomes]
rs72684485	0.84[ASN][1000 genomes]
rs72684487	0.84[ASN][1000 genomes]
rs72684488	0.84[ASN][1000 genomes]
rs72684499	0.84[ASN][1000 genomes]
rs72686404	0.84[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	nsv529677	chr1:45179509-45748571	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	424 gene(s)	inside rSNPs	diseases
2	nsv1002026	chr1:45187594-45758048	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	386 gene(s)	inside rSNPs	diseases
3	nsv915644	chr1:45282802-45696079	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
4	nsv498036	chr1:45428030-46050934	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
5	nsv945918	chr1:45642615-45660743	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45645600-45662600	Weak transcription	HepG2	liver

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