Variant report

Variant	rs10027627
Chromosome Location	chr4:120569737-120569738
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:15)

rs_ID	r²[population]
rs12331968	0.82[AFR][1000 genomes]
rs13122502	0.85[AFR][1000 genomes]
rs2257018	0.82[AFR][1000 genomes]
rs2389865	0.85[AFR][1000 genomes]
rs2389867	0.85[AFR][1000 genomes]
rs2715018	0.82[AFR][1000 genomes]
rs2715020	0.85[AFR][1000 genomes]
rs2715021	0.81[AFR][1000 genomes]
rs2715022	0.85[AFR][1000 genomes]
rs2953292	0.85[AFR][1000 genomes]
rs4264816	0.85[AFR][1000 genomes]
rs4513554	0.85[AFR][1000 genomes]
rs7670618	0.83[AFR][1000 genomes]
rs7675276	0.86[AFR][1000 genomes]
rs7697823	0.85[AFR][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	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv532739	chr4:120392824-121098103	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv1010753	chr4:120429028-120684310	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv537233	chr4:120429028-120684310	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1006572	chr4:120432494-120694243	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv1802546	chr4:120558608-120675026	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120567600-120569800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr4:120567800-120569800	Enhancers	Liver	Liver
3	chr4:120568200-120573600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:120568200-120573600	Weak transcription	NH-A	brain
5	chr4:120568400-120573600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr4:120568400-120577400	Weak transcription	Psoas Muscle	Psoas
7	chr4:120568600-120582200	Weak transcription	Fetal Brain Male	brain
8	chr4:120568800-120573200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr4:120568800-120573200	Weak transcription	NHLF	lung
10	chr4:120568800-120573600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:120569000-120573200	Weak transcription	Osteobl	bone
12	chr4:120569200-120573600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr4:120569600-120570000	Enhancers	HepG2	liver

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dbSNP/dbVar ID: rs12345 /nsv7879
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