Variant report

Variant	rs4683343
Chromosome Location	chr3:42878193-42878194
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11129985	0.87[YRI][hapmap]
rs4683347	1.00[AFR][1000 genomes]
rs9865715	0.88[YRI][hapmap]

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	esv1847016	chr3:42855765-42880490	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:42861600-42885400	Weak transcription	Pancreas	Pancrea
2	chr3:42871200-42885000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr3:42871400-42885400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr3:42873200-42880600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr3:42873200-42883000	Weak transcription	Right Atrium	heart
6	chr3:42873200-42885400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr3:42873800-42881000	Weak transcription	Adipose Nuclei	Adipose
8	chr3:42874400-42882800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr3:42877800-42878600	Flanking Active TSS	K562	blood
10	chr3:42878000-42878400	Enhancers	Fetal Heart	heart
11	chr3:42878000-42878800	Strong transcription	Placenta	Placenta

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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