Variant report

Variant	rs12699641
Chromosome Location	chr7:14573817-14573818
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10236653	0.84[CEU][hapmap];0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10237359	0.84[EUR][1000 genomes]
rs10260522	0.85[CEU][hapmap]
rs10274270	0.86[CEU][hapmap]
rs10274418	0.83[CEU][hapmap]
rs10274552	0.84[CHB][hapmap];0.86[JPT][hapmap]
rs10499442	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs11505395	0.86[CEU][hapmap]
rs11505396	0.82[CEU][hapmap]
rs11767890	0.93[CEU][hapmap];0.83[EUR][1000 genomes]
rs11767969	0.81[CEU][hapmap];0.81[EUR][1000 genomes]
rs11771647	0.81[CEU][hapmap]
rs12669548	0.85[CEU][hapmap]
rs12674261	0.88[CEU][hapmap]
rs12699622	0.88[CEU][hapmap];0.84[EUR][1000 genomes]
rs12699624	0.82[CEU][hapmap]
rs12699626	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs12699627	0.83[CEU][hapmap]
rs12699628	0.82[CEU][hapmap]
rs12699635	0.86[CEU][hapmap]
rs12699636	0.81[CEU][hapmap]
rs13232496	0.89[CEU][hapmap]
rs1367781	0.82[CEU][hapmap]
rs1431521	0.89[CEU][hapmap]
rs1431528	0.85[CEU][hapmap]
rs1431531	0.88[CHB][hapmap];0.86[ASN][1000 genomes]
rs1560576	0.81[CEU][hapmap]
rs1897300	0.85[CEU][hapmap]
rs196751	0.85[CEU][hapmap]
rs1991685	0.88[CEU][hapmap]
rs2357960	0.85[CEU][hapmap]
rs3823843	0.88[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs4370419	0.89[CEU][hapmap]
rs4719407	0.83[CEU][hapmap]
rs4719409	0.82[CEU][hapmap]
rs4721343	0.88[CHB][hapmap];0.84[AMR][1000 genomes]
rs4721345	0.89[CEU][hapmap]
rs6461104	0.88[CEU][hapmap]
rs6958607	0.89[CEU][hapmap]
rs6958691	0.96[CEU][hapmap]
rs6979012	0.89[CEU][hapmap]
rs6979330	0.89[CEU][hapmap]
rs6980167	0.89[CEU][hapmap]
rs7783571	0.84[EUR][1000 genomes]
rs7793372	0.82[CEU][hapmap]
rs7806877	0.84[CEU][hapmap]
rs7807072	0.89[CEU][hapmap]
rs987448	0.85[CEU][hapmap]
rs987449	0.88[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 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	nsv887707	chr7:14471682-14576163	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv887708	chr7:14494508-14617982	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv606282	chr7:14542836-14579801	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
7	nsv1022267	chr7:14551894-14607627	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv887709	chr7:14562957-14604898	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	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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