Variant report

Variant	rs2137986
Chromosome Location	chr13:61710566-61710567
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11148544	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11840464	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1514550	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1588805	0.90[ASN][1000 genomes]
rs3127277	0.89[ASN][1000 genomes]
rs3127281	0.88[JPT][hapmap]
rs3127285	0.89[JPT][hapmap]
rs34460520	0.88[ASN][1000 genomes]
rs34660732	0.87[ASN][1000 genomes]
rs4884374	0.88[ASN][1000 genomes]
rs4886316	0.90[ASN][1000 genomes]
rs6562159	0.87[ASN][1000 genomes]
rs6562160	0.85[AFR][1000 genomes]
rs7982120	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7982892	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7997602	0.88[EUR][1000 genomes]
rs9528296	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs9592092	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832627	chr13:61642811-61829217	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
2	esv3444432	chr13:61665252-61781081	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61709600-61711000	Enhancers	Fetal Heart	heart
2	chr13:61709800-61710600	Enhancers	Skeletal Muscle Male	skeletal muscle
3	chr13:61710200-61710600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr13:61710200-61711200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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