Variant report

Variant	rs7674832
Chromosome Location	chr4:87382743-87382744
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11929783	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11941484	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11946235	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11946258	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35455450	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6824346	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6831576	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6831589	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6845334	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7684469	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7690940	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7693558	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv594786	chr4:87076360-87609320	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv999470	chr4:87165663-87514552	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537164	chr4:87165663-87514552	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv594787	chr4:87221827-87888667	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv1012836	chr4:87279206-87643558	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 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	chr4:87381200-87382800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
2	chr4:87381200-87383600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:87381800-87382800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
4	chr4:87381800-87383000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr4:87382400-87383600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr4:87382600-87382800	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr4:87382600-87383600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr4:87382600-87384200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr4:87382600-87385000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:87382600-87387800	Weak transcription	ES-I3 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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