Variant report

Variant	rs58511995
Chromosome Location	chr3:155101013-155101014
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:9)

rs_ID	r²[population]
rs1356604	1.00[EUR][1000 genomes]
rs16824777	1.00[EUR][1000 genomes]
rs16824779	1.00[EUR][1000 genomes]
rs56122616	1.00[EUR][1000 genomes]
rs60656067	1.00[EUR][1000 genomes]
rs6768491	1.00[EUR][1000 genomes]
rs73013284	1.00[EUR][1000 genomes]
rs73873138	1.00[EUR][1000 genomes]
rs7650465	1.00[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	nsv999994	chr3:154579254-155175303	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv532664	chr3:154588346-155162615	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv1000753	chr3:154848433-155207022	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
4	nsv536773	chr3:154848433-155207022	Enhancers Strong transcription Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155097000-155109400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:155100400-155101600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr3:155100400-155101600	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr3:155100400-155101800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr3:155100600-155101200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:155100600-155101600	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr3:155100600-155101800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr3:155100600-155102200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:155100800-155101200	Enhancers	H9 Cell Line	embryonic stem cell
10	chr3:155100800-155101800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr3:155100800-155102200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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