Variant report

Variant	rs56836923
Chromosome Location	chr6:81320081-81320082
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs56305940	1.00[AMR][1000 genomes]
rs57554841	1.00[AMR][1000 genomes]
rs58855828	1.00[AMR][1000 genomes]
rs60133974	1.00[AMR][1000 genomes]
rs6917382	1.00[AMR][1000 genomes]
rs73477693	1.00[AMR][1000 genomes]
rs73479714	1.00[AMR][1000 genomes]
rs73479719	1.00[AMR][1000 genomes]
rs73479721	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73481805	1.00[AMR][1000 genomes]
rs73748658	1.00[AMR][1000 genomes]
rs9449084	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531333	chr6:81042427-81836484	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1019670	chr6:81086504-81569984	ZNF genes & repeats Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv915714	chr6:81134888-81366749	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv1020533	chr6:81288890-81406533	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv538340	chr6:81288890-81406533	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv508417	chr6:81290516-81330590	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv604085	chr6:81297890-81439973	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1015520	chr6:81309213-81374699	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:81314800-81321000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr6:81317000-81321000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:81317000-81321000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:81317000-81321000	Enhancers	HMEC	breast
5	chr6:81317000-81321000	Enhancers	HSMM	muscle
6	chr6:81317000-81321200	Enhancers	NHDF-Ad	bronchial
7	chr6:81317800-81321200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr6:81318200-81320400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:81318200-81321000	Weak transcription	Right Atrium	heart
10	chr6:81318400-81320600	Weak transcription	Hela-S3	cervix
11	chr6:81318400-81321000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:81318400-81321200	Enhancers	Muscle Satellite Cultured Cells	--
13	chr6:81318400-81321200	Enhancers	HSMMtube	muscle
14	chr6:81319200-81320200	Weak transcription	NHEK	skin
15	chr6:81320000-81320600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr6:81320000-81321000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr6:81320000-81321000	Enhancers	NHLF	lung
18	chr6:81320000-81321200	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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