Variant report

Variant	rs1531871
Chromosome Location	chr3:25407268-25407269
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs13094358	0.90[ASN][1000 genomes]
rs13325064	0.95[ASN][1000 genomes]
rs1384899	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1483842	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17588729	0.94[ASN][1000 genomes]
rs35569984	0.94[ASN][1000 genomes]
rs35946440	0.90[ASN][1000 genomes]
rs4681019	0.90[ASN][1000 genomes]
rs62235603	0.84[ASN][1000 genomes]
rs72619935	0.83[ASN][1000 genomes]
rs8180044	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9835390	0.84[ASN][1000 genomes]
rs9835396	0.84[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	nsv949035	chr3:25194301-26084890	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
2	nsv834645	chr3:25363723-25555107	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25406800-25407600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:25406800-25407600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:25406800-25407800	Enhancers	Fetal Intestine Small	intestine
4	chr3:25407200-25408000	Enhancers	Fetal Intestine Large	intestine
5	chr3:25407200-25408400	Enhancers	Fetal Heart	heart

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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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