Variant report

Variant	rs56979203
Chromosome Location	chr3:141566052-141566053
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs58449157	1.00[AMR][1000 genomes]
rs60939446	1.00[AMR][1000 genomes]
rs61327618	1.00[AMR][1000 genomes]
rs72986303	1.00[AMR][1000 genomes]
rs72986323	1.00[AMR][1000 genomes]
rs72986333	1.00[AMR][1000 genomes]
rs72986358	1.00[AMR][1000 genomes]
rs72988221	1.00[AMR][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	nsv949709	chr3:141295050-142178144	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv1013352	chr3:141541105-141870293	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141550800-141571800	Weak transcription	Esophagus	oesophagus
2	chr3:141560200-141568200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:141560600-141572600	Weak transcription	Spleen	Spleen
4	chr3:141564800-141570200	Weak transcription	Placenta	Placenta
5	chr3:141565000-141567200	Weak transcription	K562	blood
6	chr3:141565000-141572000	Weak transcription	Adipose Nuclei	Adipose
7	chr3:141565000-141578000	Weak transcription	Fetal Intestine Small	intestine
8	chr3:141565200-141569800	Weak transcription	HUVEC	blood vessel

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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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