Variant report

Variant	rs4903967
Chromosome Location	chr14:81485149-81485150
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10873332	0.87[ASN][1000 genomes]
rs12185020	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12436366	0.93[ASN][1000 genomes]
rs2268466	0.87[ASN][1000 genomes]
rs4899784	0.94[ASN][1000 genomes]
rs4903965	0.93[ASN][1000 genomes]
rs59484155	0.93[ASN][1000 genomes]
rs72689907	0.86[ASN][1000 genomes]
rs72689910	0.87[ASN][1000 genomes]
rs72695035	0.86[ASN][1000 genomes]
rs917986	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1052999	chr14:81468860-81599074	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv542144	chr14:81468860-81599074	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81455800-81492200	Weak transcription	Fetal Thymus	thymus
2	chr14:81468000-81486600	Weak transcription	Thymus	Thymus
3	chr14:81482600-81487000	Strong transcription	Dnd41	blood
4	chr14:81484000-81485600	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr14:81484400-81485200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr14:81484400-81485200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr14:81484600-81485200	Flanking Active TSS	Adipose Nuclei	Adipose
8	chr14:81484600-81502400	Weak transcription	Liver	Liver
9	chr14:81484800-81485800	Enhancers	K562	blood
10	chr14:81485000-81485200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr14:81485000-81485400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr14:81485000-81485600	Enhancers	Primary neutrophils fromperipheralblood	blood

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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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