Variant report

Variant	rs10096651
Chromosome Location	chr8:124758733-124758734
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs4870865	0.83[EUR][1000 genomes]
rs7460871	0.95[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831451	chr8:124710946-124885148	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv6373	chr8:124741567-124786609	Active TSS Genic enhancers Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124746800-124763600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr8:124756400-124761400	Weak transcription	NHEK	skin
3	chr8:124757400-124761600	Weak transcription	A549	lung
4	chr8:124757800-124761200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr8:124757800-124764600	Weak transcription	Small Intestine	intestine
6	chr8:124758000-124759400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr8:124758000-124759600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr8:124758000-124760000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr8:124758200-124759200	Weak transcription	Fetal Intestine Large	intestine
10	chr8:124758200-124759800	Weak transcription	HepG2	liver
11	chr8:124758400-124759600	Weak transcription	Fetal Intestine Small	intestine

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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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