Variant report

Variant	rs7631249
Chromosome Location	chr3:140283768-140283769
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10755093	0.85[AFR][1000 genomes]
rs10804675	0.86[JPT][hapmap]
rs10935386	0.86[JPT][hapmap]
rs11714465	0.86[JPT][hapmap];1.00[YRI][hapmap]
rs11916215	0.88[JPT][hapmap]
rs12494698	0.86[JPT][hapmap]
rs13078522	0.86[JPT][hapmap]
rs4683509	0.86[JPT][hapmap]
rs4683510	0.86[JPT][hapmap]
rs6762605	1.00[YRI][hapmap]
rs961554	1.00[YRI][hapmap]
rs9845717	0.88[JPT][hapmap]
rs9851873	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757891	chr3:139925764-140524730	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	esv2759181	chr3:139925764-140524730	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv527831	chr3:139932966-140533823	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv34489	chr3:140009020-140469302	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv2757012	chr3:140009220-140460228	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv870185	chr3:140265153-140395673	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr3:140265600-140287800	Weak transcription	Pancreas	Pancrea
2	chr3:140274200-140287600	Weak transcription	Brain Hippocampus Middle	brain
3	chr3:140279200-140288400	Strong transcription	HSMMtube	muscle
4	chr3:140279600-140289600	Weak transcription	Fetal Brain Female	brain
5	chr3:140280400-140286200	Strong transcription	Ovary	ovary
6	chr3:140280800-140286200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:140281000-140287800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr3:140282400-140287600	Weak transcription	Adipose Nuclei	Adipose
9	chr3:140282800-140288000	Weak transcription	Liver	Liver
10	chr3:140283200-140285000	Weak transcription	H1 BMP4 Derived Trophoblast 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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