Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10241762	1.00[ASW][hapmap]
rs10242478	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10267135	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10950524	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12666188	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12668508	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12670156	1.00[CHB][hapmap]
rs12671101	1.00[JPT][hapmap]
rs16878148	1.00[EUR][1000 genomes]
rs17168223	1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17168227	1.00[CHB][hapmap];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs196747	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs196752	0.85[MEX][hapmap]
rs196754	0.94[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap]
rs196763	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4721339	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4721340	0.80[AMR][1000 genomes]
rs6943504	1.00[EUR][1000 genomes]
rs6957588	0.82[CHB][hapmap];0.86[ASN][1000 genomes]
rs6971925	1.00[MEX][hapmap]
rs73282311	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73282318	0.82[AMR][1000 genomes]
rs73282321	0.82[AMR][1000 genomes]
rs73285809	0.93[ASN][1000 genomes]
rs7782300	0.88[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 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

No data

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

No data

Quick Search:

Input of quick search could be: