Variant report

Variant	rs4440237
Chromosome Location	chr4:130308216-130308217
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12506624	0.86[ASN][1000 genomes]
rs12506696	0.86[ASN][1000 genomes]
rs12510624	0.88[ASN][1000 genomes]
rs1433378	0.99[ASN][1000 genomes]
rs17014735	0.92[ASN][1000 genomes]
rs4540061	0.97[ASN][1000 genomes]
rs56361313	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61554187	0.98[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs62309611	0.96[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs62309616	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534538	chr4:129799138-130431688	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv830058	chr4:130136025-130315471	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:130308200-130308400	Flanking Active TSS	Fetal Heart	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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