Variant report

Variant	rs1425331
Chromosome Location	chr4:21257287-21257288
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11722925	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11722994	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11724880	0.84[JPT][hapmap]
rs11735059	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13128130	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13128781	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13146289	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs1425330	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1425344	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs1485514	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs1485517	0.84[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap]
rs1545915	0.84[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap]
rs1872458	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs1872459	0.84[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap]
rs1872461	0.84[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap]
rs2059488	1.00[CHB][hapmap]
rs2322883	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs2322884	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs28591172	0.84[ASN][1000 genomes]
rs2874896	0.89[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap]
rs34595298	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35921744	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4697213	1.00[CEU][hapmap]
rs6827486	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6828595	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6829425	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6850742	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs901112	0.84[CEU][hapmap]
rs901113	0.84[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014941	chr4:20611726-21345226	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537053	chr4:20611726-21345226	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	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
4	nsv1002610	chr4:21192993-21261812	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	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
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