Variant report

Variant	rs1522853
Chromosome Location	chr8:34614677-34614678
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11988462	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs11995347	0.86[ASN][1000 genomes]
rs12114068	0.86[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs13254921	0.82[ASN][1000 genomes]
rs13262347	0.82[ASN][1000 genomes]
rs13263701	0.88[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs13264659	0.86[ASN][1000 genomes]
rs1403377	0.86[ASN][1000 genomes]
rs1522844	0.88[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs1522849	0.86[ASN][1000 genomes]
rs1522850	0.86[ASN][1000 genomes]
rs1916172	0.86[ASN][1000 genomes]
rs1916173	0.86[ASN][1000 genomes]
rs1916175	0.86[ASN][1000 genomes]
rs1949719	0.86[ASN][1000 genomes]
rs1949720	0.84[ASN][1000 genomes]
rs1949721	0.86[ASN][1000 genomes]
rs2685590	0.84[ASN][1000 genomes]
rs2685591	0.84[ASN][1000 genomes]
rs2685599	0.84[ASN][1000 genomes]
rs2685600	0.84[ASN][1000 genomes]
rs2685607	0.84[ASN][1000 genomes]
rs2687554	0.84[ASN][1000 genomes]
rs2687556	0.84[ASN][1000 genomes]
rs2687557	0.84[ASN][1000 genomes]
rs35383581	0.82[ASN][1000 genomes]
rs6468286	0.86[ASN][1000 genomes]
rs6468288	0.84[ASN][1000 genomes]
rs6468289	0.84[ASN][1000 genomes]
rs6994824	0.86[ASN][1000 genomes]
rs7007425	0.86[ASN][1000 genomes]
rs7843303	0.86[ASN][1000 genomes]
rs7845916	0.84[ASN][1000 genomes]
rs952902	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831283	chr8:34501243-34662634	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv525800	chr8:34568015-34615454	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv890715	chr8:34568015-34700530	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv1815008	chr8:34577042-34615454	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv1810036	chr8:34577042-34620708	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3326932	chr8:34613510-34617008	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3422722	chr8:34613960-34616958	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34613200-34615400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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