Variant report

Variant	rs8179903
Chromosome Location	chr3:111547319-111547320
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1039309	1.00[AMR][1000 genomes]
rs10755070	1.00[AMR][1000 genomes]
rs12171297	1.00[AMR][1000 genomes]
rs1282969	1.00[AMR][1000 genomes]
rs1282971	1.00[AMR][1000 genomes]
rs1352888	1.00[AMR][1000 genomes]
rs1463875	1.00[AMR][1000 genomes]
rs1553226	1.00[AMR][1000 genomes]
rs2055363	1.00[AMR][1000 genomes]
rs28809607	1.00[AMR][1000 genomes]
rs4682064	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7340688	1.00[AMR][1000 genomes]
rs7616227	1.00[AMR][1000 genomes]
rs7644889	1.00[AMR][1000 genomes]
rs937555	1.00[AMR][1000 genomes]
rs937556	1.00[AMR][1000 genomes]
rs937558	1.00[AMR][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	nsv829676	chr3:111464087-111619200	Genic enhancers Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111541000-111550600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:111541200-111577600	Weak transcription	Pancreas	Pancrea
3	chr3:111543800-111550800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr3:111544200-111547400	Enhancers	Placenta	Placenta
5	chr3:111544400-111556800	Weak transcription	Liver	Liver
6	chr3:111545800-111550800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr3:111545800-111550800	Weak transcription	NHEK	skin
8	chr3:111546200-111550400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr3:111546200-111550600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr3:111546200-111550600	Weak transcription	HMEC	breast
11	chr3:111546200-111550800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr3:111546600-111547800	Enhancers	Adipose Nuclei	Adipose
13	chr3:111546800-111547600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:111546800-111549000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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