Variant report

Variant	rs10733322
Chromosome Location	chr9:16841777-16841778
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10435764	1.00[AMR][1000 genomes]
rs10733324	1.00[AMR][1000 genomes]
rs10756821	1.00[AMR][1000 genomes]
rs10756837	1.00[AMR][1000 genomes]
rs1416740	1.00[AMR][1000 genomes]
rs1832550	1.00[AMR][1000 genomes]
rs2095881	1.00[AMR][1000 genomes]
rs3861710	1.00[AMR][1000 genomes]
rs4246132	1.00[AMR][1000 genomes]
rs4327939	1.00[AMR][1000 genomes]
rs4961423	1.00[AMR][1000 genomes]
rs4961424	1.00[AMR][1000 genomes]
rs4961500	1.00[AMR][1000 genomes]
rs4961504	1.00[AMR][1000 genomes]
rs7032936	1.00[AMR][1000 genomes]
rs7039999	1.00[AMR][1000 genomes]
rs7048224	1.00[AMR][1000 genomes]
rs7847859	1.00[AMR][1000 genomes]
rs7862159	1.00[AMR][1000 genomes]
rs7868036	1.00[AMR][1000 genomes]
rs8181207	1.00[AMR][1000 genomes]
rs9695691	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024799	chr9:16631890-17431827	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv892650	chr9:16696187-16950860	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv892651	chr9:16816755-16869240	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16829200-16852800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:16829800-16864200	Weak transcription	NH-A	brain
3	chr9:16831000-16859600	Weak transcription	HSMM	muscle
4	chr9:16831200-16852600	Weak transcription	Fetal Lung	lung
5	chr9:16831200-16863400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr9:16831200-16864400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr9:16833800-16863800	Weak transcription	NHLF	lung
8	chr9:16834600-16852600	Weak transcription	Fetal Stomach	stomach
9	chr9:16835200-16848400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr9:16836200-16864400	Weak transcription	NHDF-Ad	bronchial
11	chr9:16838200-16842400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr9:16838800-16852000	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr9:16839200-16846400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr9:16839800-16842200	Enhancers	Colon Smooth Muscle	Colon
15	chr9:16840200-16842600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr9:16840400-16852000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr9:16840600-16849400	Weak transcription	Ovary	ovary
18	chr9:16841000-16848200	Weak transcription	iPS-15b Cell Line	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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