Variant report

Variant	rs2390564
Chromosome Location	chr4:124569266-124569267
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs1425419	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1425420	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59812456	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7695956	1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]

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	esv34581	chr4:124271321-125247395	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv469710	chr4:124474286-124623722	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv482747	chr4:124474286-124623722	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv830047	chr4:124504051-124699142	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv879873	chr4:124528452-124590869	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv879874	chr4:124550693-124607201	Genic enhancers Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:124558400-124569800	Weak transcription	Psoas Muscle	Psoas
2	chr4:124564800-124570000	Weak transcription	Fetal Kidney	kidney
3	chr4:124565000-124570400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:124565200-124570200	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr4:124565200-124570600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr4:124565200-124570600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr4:124565200-124570600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr4:124565400-124570200	Weak transcription	Colon Smooth Muscle	Colon
9	chr4:124565400-124570600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr4:124565600-124570400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:124566000-124570400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr4:124568600-124570800	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr4:124568800-124570400	Enhancers	HepG2	liver
14	chr4:124569200-124569400	Enhancers	Fetal Muscle Trunk	muscle
15	chr4:124569200-124569600	Weak transcription	Fetal Muscle Leg	muscle
16	chr4:124569200-124570200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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