Variant report

Variant	rs7460910
Chromosome Location	chr8:121919361-121919362
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1317511	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2386128	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55900967	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57024511	0.97[ASN][1000 genomes]
rs58793775	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59972267	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73710114	1.00[EUR][1000 genomes];0.97[ASN][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	nsv1016172	chr8:121679590-121929916	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv891423	chr8:121847643-121994660	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv465790	chr8:121853405-122185415	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv612114	chr8:121853405-122185415	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv891424	chr8:121873345-122393258	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv891425	chr8:121875083-122025559	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv528893	chr8:121914565-121928562	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121918000-121920200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:121918200-121919400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr8:121918600-121919600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr8:121918800-121920000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:121918800-121920000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr8:121918800-121920000	Enhancers	HSMM	muscle
7	chr8:121919000-121919400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr8:121919000-121919400	Enhancers	Adipose Nuclei	Adipose
9	chr8:121919000-121919400	Bivalent Enhancer	NHDF-Ad	bronchial
10	chr8:121919000-121919400	Enhancers	Osteobl	bone
11	chr8:121919000-121919600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr8:121919000-121920000	Enhancers	HSMMtube	muscle
13	chr8:121919000-121920200	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr8:121919200-121919400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr8:121919200-121921600	Weak transcription	Psoas Muscle	Psoas

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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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