Variant report

Variant	rs7761638
Chromosome Location	chr6:70613696-70613697
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs4457128	1.00[MEX][hapmap]
rs6899856	1.00[AMR][1000 genomes]
rs6918912	1.00[MEX][hapmap]
rs6926567	1.00[MEX][hapmap]
rs6941069	1.00[MEX][hapmap]
rs9454898	1.00[MEX][hapmap]
rs9454928	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9454931	1.00[AMR][1000 genomes]
rs9454934	1.00[AMR][1000 genomes]
rs9454940	1.00[YRI][hapmap]
rs991974	1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886140	chr6:70354682-70728202	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv886141	chr6:70590638-70694162	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70604400-70617800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:70605200-70616000	Weak transcription	Fetal Stomach	stomach
3	chr6:70605600-70627800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:70609800-70616400	Strong transcription	Primary B cells from peripheral blood	blood
5	chr6:70609800-70616800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr6:70610800-70618200	Strong transcription	Primary B cells from cord blood	blood
7	chr6:70613400-70615200	Strong transcription	GM12878-XiMat	blood
8	chr6:70613600-70616200	Weak transcription	Primary mononuclear cells 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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