Variant report

Variant	rs36055767
Chromosome Location	chr20:15623233-15623234
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs6131683	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6131684	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6131685	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][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	nsv869328	chr20:15325423-16213898	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv2751909	chr20:15489871-15656007	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv833928	chr20:15619962-15780758	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:15617600-15629000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr20:15619400-15629200	Weak transcription	Colon Smooth Muscle	Colon
3	chr20:15619400-15634600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr20:15621000-15623600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr20:15622600-15624000	Enhancers	Aorta	Aorta
6	chr20:15622800-15623600	Enhancers	Fetal Kidney	kidney
7	chr20:15622800-15624200	Enhancers	HUVEC	blood vessel
8	chr20:15623000-15624000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr20:15623000-15624200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr20:15623200-15623600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr20:15623200-15623600	Enhancers	Brain Substantia Nigra	brain
12	chr20:15623200-15623800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr20:15623200-15624000	Enhancers	Muscle Satellite Cultured Cells	--

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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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