Variant report

Variant	rs10497486
Chromosome Location	chr2:178711888-178711889
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10497485	1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1370658	1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1527292	1.00[AMR][1000 genomes]
rs16865829	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865833	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865835	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865838	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865839	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865844	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865848	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865850	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865852	1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16865872	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs16865887	1.00[AMR][1000 genomes]
rs16865907	1.00[AMR][1000 genomes]
rs16865909	1.00[AMR][1000 genomes]
rs16865918	1.00[AMR][1000 genomes]
rs16865933	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999086	chr2:178262348-178773585	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv536055	chr2:178262348-178773585	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv583690	chr2:178638381-178712283	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv3053	chr2:178690640-178735132	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	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	chr2:178699800-178716600	Weak transcription	Skeletal Muscle Female	skeletal muscle

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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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