Variant report

Variant	rs10088713
Chromosome Location	chr8:52923780-52923781
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10104090	0.91[CHB][hapmap];0.92[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];0.86[TSI][hapmap];0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10105814	0.82[ASN][1000 genomes]
rs10106301	0.95[ASN][1000 genomes]
rs4873633	0.81[ASN][1000 genomes]
rs6988634	0.91[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73593042	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73679114	0.80[ASN][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	nsv817615	chr8:52252405-53023384	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:52921200-52924400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr8:52921200-52924400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr8:52921200-52926600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:52921200-52932800	Weak transcription	Pancreas	Pancrea
5	chr8:52921600-52924400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr8:52921600-52924400	Weak transcription	Dnd41	blood
7	chr8:52922400-52924400	Weak transcription	Osteobl	bone
8	chr8:52923200-52924200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:52923200-52924200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr8:52923200-52924200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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