Variant report

Variant	rs12670458
Chromosome Location	chr7:14579051-14579052
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10231750	0.92[CEU][hapmap]
rs10235540	0.88[CEU][hapmap];0.85[CHB][hapmap];0.81[JPT][hapmap]
rs10244094	0.82[CEU][hapmap]
rs10245171	0.87[CEU][hapmap]
rs10245903	0.82[CEU][hapmap]
rs10247453	0.85[CEU][hapmap];0.90[CHB][hapmap];0.85[JPT][hapmap];0.81[EUR][1000 genomes]
rs10256038	0.85[CEU][hapmap]
rs10263131	0.88[CEU][hapmap];0.89[CHB][hapmap];0.81[JPT][hapmap];0.80[EUR][1000 genomes]
rs10270441	0.81[CEU][hapmap]
rs1030578	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs10499441	0.88[CEU][hapmap];0.90[CHB][hapmap];0.81[JPT][hapmap];0.81[EUR][1000 genomes]
rs11762226	0.89[CEU][hapmap]
rs11767969	0.81[CEU][hapmap]
rs11771647	0.81[CEU][hapmap]
rs11771951	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs11982590	0.95[CEU][hapmap]
rs12154477	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs12699617	0.81[CEU][hapmap]
rs12699618	0.89[CEU][hapmap]
rs12699619	0.88[CEU][hapmap];0.80[EUR][1000 genomes]
rs12699621	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs12699624	0.88[CEU][hapmap]
rs12699625	0.90[CEU][hapmap]
rs12699626	0.82[CEU][hapmap]
rs12699627	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs12699628	0.88[CEU][hapmap];0.83[EUR][1000 genomes]
rs12699629	0.92[CEU][hapmap]
rs12699635	0.86[CEU][hapmap]
rs12699636	0.88[CEU][hapmap]
rs13238777	0.81[EUR][1000 genomes]
rs13243691	0.89[CEU][hapmap]
rs13438642	0.81[CEU][hapmap]
rs1367780	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1367781	0.88[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1367783	0.81[CEU][hapmap]
rs1431520	0.84[CEU][hapmap];0.85[CHB][hapmap];0.81[JPT][hapmap]
rs1431525	0.88[CEU][hapmap];0.90[CHB][hapmap];0.81[JPT][hapmap]
rs1431526	0.87[CEU][hapmap]
rs1431527	0.89[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap]
rs1431532	0.92[CEU][hapmap]
rs1431538	0.92[CEU][hapmap]
rs1541874	0.89[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap]
rs1978671	0.83[CEU][hapmap];0.83[EUR][1000 genomes]
rs2116314	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs2116315	0.95[CEU][hapmap]
rs2116319	1.00[CEU][hapmap]
rs2884348	0.88[CEU][hapmap];0.82[EUR][1000 genomes]
rs34919207	0.80[EUR][1000 genomes]
rs4607508	0.86[EUR][1000 genomes]
rs4719405	0.81[EUR][1000 genomes]
rs4719406	0.86[CEU][hapmap];0.89[CHB][hapmap];0.80[JPT][hapmap];0.81[EUR][1000 genomes]
rs4719407	0.89[CEU][hapmap]
rs4719409	0.89[CEU][hapmap]
rs4721335	0.88[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap];0.81[EUR][1000 genomes]
rs4721336	0.81[EUR][1000 genomes]
rs4721337	0.81[EUR][1000 genomes]
rs4721338	0.88[CEU][hapmap];0.90[JPT][hapmap]
rs4721342	0.92[CEU][hapmap]
rs6461102	0.89[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap]
rs6943928	0.89[CEU][hapmap]
rs6975021	0.82[CEU][hapmap]
rs7777868	0.87[EUR][1000 genomes]
rs7782805	0.92[CEU][hapmap];0.84[EUR][1000 genomes]
rs7783911	0.80[EUR][1000 genomes]
rs7793372	0.88[CEU][hapmap];0.90[CHB][hapmap];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7794554	0.82[EUR][1000 genomes]
rs9690425	0.88[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 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	esv1848567	chr7:14464118-14579801	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv887708	chr7:14494508-14617982	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv606282	chr7:14542836-14579801	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
6	nsv1022267	chr7:14551894-14607627	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv887709	chr7:14562957-14604898	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	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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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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