Variant report

Variant	rs74105624
Chromosome Location	chr13:87896651-87896652
allele	C/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]
rs58044864	1.00[AFR][1000 genomes]
rs59690989	0.90[AFR][1000 genomes]
rs59949878	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60144006	0.80[AFR][1000 genomes]
rs60609846	0.82[AFR][1000 genomes]
rs73558883	0.90[AFR][1000 genomes]
rs73561226	0.82[AFR][1000 genomes]
rs73561227	0.82[AFR][1000 genomes]
rs73562444	1.00[AFR][1000 genomes]
rs73562449	1.00[AFR][1000 genomes]
rs73562451	1.00[AFR][1000 genomes]
rs73562479	0.86[AFR][1000 genomes]
rs73562486	0.84[AFR][1000 genomes]
rs74103207	0.90[AFR][1000 genomes]
rs74103288	0.90[AFR][1000 genomes]
rs74103297	0.90[AFR][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	nsv562621	chr13:87192747-87927450	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1045687	chr13:87822969-88114685	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv541860	chr13:87822969-88114685	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv930999	chr13:87831662-88143592	Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1047914	chr13:87835419-87909531	Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1043448	chr13:87835419-88140970	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv916254	chr13:87856806-88107725	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:87886000-87907600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:87896200-87897200	Enhancers	Primary hematopoietic stem cells	blood
3	chr13:87896400-87896800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr13:87896400-87897000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr13:87896400-87897000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr13:87896400-87897400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr13:87896400-87897600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr13:87896600-87897000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr13:87896600-87897000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr13:87896600-87897000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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