Variant report

Variant	rs73280840
Chromosome Location	chr8:102880884-102880885
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs58196146	1.00[AMR][1000 genomes]
rs58704718	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60341429	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73280814	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73280829	1.00[AMR][1000 genomes]
rs73280834	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73280843	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73280869	1.00[AMR][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	nsv1018653	chr8:102818271-103009082	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv539700	chr8:102818271-103009082	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv518162	chr8:102841031-102893626	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv523850	chr8:102841031-102893626	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv465749	chr8:102847202-102929460	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv611819	chr8:102847202-102929460	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1030076	chr8:102866179-102896458	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:102870000-102891200	Weak transcription	Ovary	ovary
2	chr8:102876600-102883400	Weak transcription	NHDF-Ad	bronchial
3	chr8:102879000-102881000	Enhancers	Small Intestine	intestine
4	chr8:102879000-102881000	Enhancers	Stomach Mucosa	stomach
5	chr8:102880200-102881400	Enhancers	Aorta	Aorta
6	chr8:102880400-102881000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr8:102880400-102881000	Enhancers	Fetal Intestine Large	intestine
8	chr8:102880400-102881000	Genic enhancers	Fetal Muscle Leg	muscle
9	chr8:102880400-102881400	Enhancers	Psoas Muscle	Psoas
10	chr8:102880600-102881600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:102880600-102887400	Weak transcription	Fetal Muscle Trunk	muscle
12	chr8:102880800-102881800	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
13	chr8:102880800-102882600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:102880800-102885000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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