Variant report

Variant	rs10056370
Chromosome Location	chr5:107986721-107986722
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10057764	0.80[ASN][1000 genomes]
rs10069339	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1508783	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1573993	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17161424	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2221670	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28369260	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57292082	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6594327	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6890407	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6890589	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7448463	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7704945	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9326742	0.86[EUR][1000 genomes];0.96[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	nsv882689	chr5:107595383-108299744	Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv1019409	chr5:107934028-107991426	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	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	chr5:107984200-107987800	Enhancers	NHDF-Ad	bronchial
2	chr5:107985000-107989800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr5:107985200-107989400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:107985400-107990600	Enhancers	HUVEC	blood vessel
5	chr5:107985600-107989400	Weak transcription	NHLF	lung
6	chr5:107985600-107990200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr5:107986000-107987200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr5:107986400-107986800	Weak transcription	Aorta	Aorta
9	chr5:107986400-107987600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr5:107986600-107987400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	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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