Variant report

Variant	rs6767942
Chromosome Location	chr3:116143809-116143810
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10513826	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4831097	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67644980	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6777473	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7638540	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9857124	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][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	esv2757886	chr3:116142130-116307542	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv2759171	chr3:116142130-116307542	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:116142200-116144200	Enhancers	Stomach Mucosa	stomach
2	chr3:116142800-116144000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
3	chr3:116142800-116144000	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr3:116143000-116144000	Enhancers	Brain Anterior Caudate	brain
5	chr3:116143000-116144200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr3:116143000-116144200	Enhancers	Brain Angular Gyrus	brain
7	chr3:116143000-116144400	Enhancers	Brain Substantia Nigra	brain
8	chr3:116143200-116144200	Enhancers	Brain Cingulate Gyrus	brain
9	chr3:116143200-116144200	Enhancers	Brain Hippocampus Middle	brain
10	chr3:116143200-116144200	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr3:116143400-116144400	Enhancers	Colon Smooth Muscle	Colon
12	chr3:116143400-116161200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr3:116143600-116161000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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