Variant report

Variant	rs4426713
Chromosome Location	chr3:144677113-144677114
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10804698	0.89[AMR][1000 genomes]
rs11714435	0.89[AMR][1000 genomes]
rs4254701	0.89[AMR][1000 genomes]
rs4362764	0.89[AMR][1000 genomes]
rs4381987	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4405957	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4541446	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4681642	0.89[AMR][1000 genomes]
rs61294843	0.89[AMR][1000 genomes]
rs6440286	0.89[AMR][1000 genomes]
rs6440289	0.89[AMR][1000 genomes]
rs6440290	0.89[AMR][1000 genomes]
rs6440311	0.89[AMR][1000 genomes]
rs6765625	0.89[AMR][1000 genomes]
rs6767341	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6778480	0.89[AMR][1000 genomes]
rs6782683	0.89[AMR][1000 genomes]
rs6788584	0.84[AMR][1000 genomes]
rs6794760	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6800640	1.00[ASN][1000 genomes]
rs7427359	0.89[AMR][1000 genomes]
rs7427634	0.89[AMR][1000 genomes]
rs7427709	0.89[AMR][1000 genomes]
rs7611410	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7619338	0.89[AMR][1000 genomes]
rs7623306	0.89[AMR][1000 genomes]
rs7624601	0.89[AMR][1000 genomes]
rs7646371	0.89[AMR][1000 genomes]
rs9289690	0.89[AMR][1000 genomes]
rs9827899	0.89[AMR][1000 genomes]
rs9828040	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9843234	0.89[AMR][1000 genomes]
rs9863285	0.89[AMR][1000 genomes]
rs9865339	0.89[AMR][1000 genomes]
rs9877095	0.89[AMR][1000 genomes]
rs9917709	0.89[AMR][1000 genomes]

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	nsv591928	chr3:144050897-144822081	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv3357831	chr3:144433846-144790831	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3405013	chr3:144433866-144790801	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1005754	chr3:144529346-144984363	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1004792	chr3:144658885-145191801	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	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	chr3:144677000-144677200	Enhancers	Colon Smooth Muscle	Colon

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