Variant report

Variant	rs74138229
Chromosome Location	chr10:44649937-44649938
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs57992999	1.00[AMR][1000 genomes]
rs74138232	1.00[AMR][1000 genomes]
rs74138237	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74138265	0.84[AFR][1000 genomes]
rs74138987	1.00[AMR][1000 genomes]
rs74140606	1.00[AMR][1000 genomes]
rs74140629	1.00[AMR][1000 genomes]
rs74140630	1.00[AMR][1000 genomes]
rs74140632	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038511	chr10:44596885-44870030	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 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	chr10:44649200-44650200	Enhancers	NHDF-Ad	bronchial
2	chr10:44649400-44650200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr10:44649600-44650000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr10:44649800-44650000	Enhancers	Ovary	ovary
5	chr10:44649800-44650200	Enhancers	Left Ventricle	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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