Variant report

Variant	rs264302
Chromosome Location	chr4:96528494-96528495
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10013356	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11941922	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1436572	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1436592	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17024225	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs183813	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs264301	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4529056	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6848675	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7681706	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]

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	esv2648717	chr4:96527343-96529922	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv2404517	chr4:96528231-96529879	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3465762	chr4:96528284-96529799	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3465758	chr4:96528336-96529769	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3465759	chr4:96528341-96529760	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3465760	chr4:96528356-96529719	Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3465761	chr4:96528410-96529690	Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3465763	chr4:96528424-96529686	Enhancers	n/a	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	chr4:96527800-96528600	Enhancers	Primary hematopoietic stem cells short term culture	blood

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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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