Variant report

Variant	rs2370049
Chromosome Location	chr3:132960772-132960773
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11914347	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs1197280	0.95[AFR][1000 genomes]
rs1398761	0.97[AFR][1000 genomes]
rs1513369	0.98[AFR][1000 genomes]
rs1708388	0.95[AFR][1000 genomes]
rs1795109	0.95[AFR][1000 genomes]
rs1913283	0.98[AFR][1000 genomes]
rs2048628	0.81[AFR][1000 genomes]
rs2370047	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs2699871	0.95[AFR][1000 genomes]
rs2887728	0.95[AFR][1000 genomes]
rs3948082	0.83[AMR][1000 genomes]
rs4298040	0.93[AFR][1000 genomes]
rs4416380	0.89[AFR][1000 genomes]
rs4498042	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4618219	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs4854575	0.83[AMR][1000 genomes]
rs6439397	0.84[AFR][1000 genomes]
rs6439399	0.93[AFR][1000 genomes]
rs6768513	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7613727	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7624059	0.97[AFR][1000 genomes]
rs938232	0.84[AFR][1000 genomes]
rs938233	0.97[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530055	chr3:132380878-132982343	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:132957200-132981400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:132958200-132967200	Weak transcription	Fetal Lung	lung

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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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