Variant report

Variant	rs1495508
Chromosome Location	chr4:21392977-21392978
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10014861	0.87[YRI][hapmap]
rs12513069	0.91[CEU][hapmap]
rs12641447	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs1390262	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs1495521	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs17522139	1.00[CEU][hapmap];0.95[CHB][hapmap];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1826738	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1845694	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1948519	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2132274	0.94[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs2322941	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap]
rs28520752	0.98[EUR][1000 genomes]
rs6448050	1.00[ASW][hapmap];0.87[YRI][hapmap]
rs6820035	0.95[CEU][hapmap]
rs7660556	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs7671666	0.91[CEU][hapmap]
rs9996172	1.00[CHB][hapmap];0.95[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1014062	chr4:21270358-21479027	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1005453	chr4:21295066-21454143	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No data

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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