Variant report

Variant	rs12537437
Chromosome Location	chr7:14581307-14581308
allele	A/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:16)

rs_ID	r²[population]
rs10499448	0.88[CHB][hapmap];0.83[JPT][hapmap]
rs10499451	1.00[CEU][hapmap];0.88[CHB][hapmap];0.94[JPT][hapmap]
rs12533796	1.00[CEU][hapmap]
rs12536087	1.00[CEU][hapmap]
rs12537102	1.00[CEU][hapmap]
rs12537358	1.00[CEU][hapmap];0.88[CHB][hapmap];0.94[JPT][hapmap]
rs12537383	1.00[CEU][hapmap];0.88[CHB][hapmap]
rs12538204	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12666606	1.00[CEU][hapmap];0.94[CHB][hapmap];0.82[JPT][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12667053	1.00[CEU][hapmap];0.94[CHB][hapmap];0.82[JPT][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17168246	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs17168250	0.88[CHB][hapmap];0.82[JPT][hapmap]
rs17168255	1.00[CEU][hapmap];0.94[CHB][hapmap];0.82[JPT][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17168261	0.87[CHB][hapmap];0.86[JPT][hapmap]
rs17168263	1.00[CEU][hapmap];0.82[CHB][hapmap];0.82[JPT][hapmap]
rs1991690	0.81[CHB][hapmap];0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv915603	chr7:14443884-14624268	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv887708	chr7:14494508-14617982	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1022267	chr7:14551894-14607627	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv887709	chr7:14562957-14604898	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3377324	chr7:14569761-14587173	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No data

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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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