Variant report

Variant	rs55871537
Chromosome Location	chr15:39101945-39101946
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs55683619	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55848257	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57258498	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57443394	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60229326	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60528415	1.00[AMR][1000 genomes]
rs7175243	1.00[AMR][1000 genomes]
rs7176607	1.00[AMR][1000 genomes]
rs73392402	0.82[AFR][1000 genomes]
rs73394130	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73394152	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73394179	1.00[AMR][1000 genomes]
rs73394182	1.00[AMR][1000 genomes]
rs74009918	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74009919	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74009920	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046994	chr15:38806163-39239014	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv832975	chr15:39011915-39227590	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1054810	chr15:39019900-39578526	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv542359	chr15:39019900-39578526	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv904087	chr15:39065424-39117186	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv510659	chr15:39072035-39148591	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv904088	chr15:39081717-39117186	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:39100600-39102000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr15:39101600-39102200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr15:39101600-39102200	Enhancers	Fetal Heart	heart
4	chr15:39101600-39102200	Enhancers	Fetal Stomach	stomach
5	chr15:39101800-39103600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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

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