Variant report

Variant	rs73812523
Chromosome Location	chr4:31090094-31090095
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11937701	1.00[EUR][1000 genomes]
rs11939049	1.00[EUR][1000 genomes]
rs12502649	1.00[EUR][1000 genomes]
rs12511624	1.00[EUR][1000 genomes]
rs12512723	1.00[EUR][1000 genomes]
rs12512727	1.00[EUR][1000 genomes]
rs55918443	1.00[EUR][1000 genomes]
rs56225968	1.00[EUR][1000 genomes]
rs56385830	1.00[EUR][1000 genomes]
rs56706315	1.00[EUR][1000 genomes]
rs59407249	1.00[EUR][1000 genomes]
rs60444821	1.00[EUR][1000 genomes]
rs61138265	1.00[EUR][1000 genomes]
rs73113475	1.00[EUR][1000 genomes]
rs73113481	1.00[EUR][1000 genomes]
rs73113482	1.00[EUR][1000 genomes]
rs73812529	1.00[EUR][1000 genomes]
rs73812530	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73812541	1.00[EUR][1000 genomes]
rs73812545	1.00[EUR][1000 genomes]
rs73812546	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73812557	1.00[EUR][1000 genomes]
rs73812563	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv1007884	chr4:31071934-31680623	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1007145	chr4:31079681-31670541	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 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	chr4:31085200-31092600	Enhancers	Fetal Heart	heart
2	chr4:31087000-31096000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr4:31087600-31090200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr4:31087800-31091400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:31088000-31091400	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr4:31088000-31092600	Enhancers	HUVEC	blood vessel
7	chr4:31088800-31091200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr4:31088800-31105200	Weak transcription	Fetal Lung	lung
9	chr4:31089000-31090600	Weak transcription	Stomach Smooth Muscle	stomach
10	chr4:31089000-31099800	Weak transcription	Aorta	Aorta
11	chr4:31089400-31092600	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr4:31089800-31091800	Enhancers	NH-A	brain
13	chr4:31089800-31091800	Enhancers	NHLF	lung
14	chr4:31090000-31091800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:31090000-31091800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:31090000-31091800	Enhancers	Hela-S3	cervix

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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