Variant report

Variant	rs67140761
Chromosome Location	chr8:62063188-62063189
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11778157	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12541340	0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12545360	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs17764366	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17831865	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2003204	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2017819	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2116466	0.87[ASN][1000 genomes]
rs2116468	0.87[ASN][1000 genomes]
rs2163609	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4033372	0.81[ASN][1000 genomes]
rs55901932	0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs56146367	0.81[ASN][1000 genomes]
rs62524553	0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7822608	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7830295	0.81[EUR][1000 genomes]
rs7830680	0.82[AFR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948922	chr8:61818964-62475097	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv465698	chr8:62036793-62179465	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv611426	chr8:62036793-62179465	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1026243	chr8:62039073-62101123	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 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	chr8:62062200-62063600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:62062200-62063800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:62062600-62063400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:62062800-62063400	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr8:62063000-62063400	Enhancers	GM12878-XiMat	blood
6	chr8:62063000-62063600	Weak transcription	Fetal Brain Female	brain
7	chr8:62063000-62065800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr8:62063000-62066200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr8:62063000-62066200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr8:62063000-62084600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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