Variant report

Variant	rs67420747
Chromosome Location	chr3:179692712-179692713
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10804882	0.93[ASN][1000 genomes]
rs11715337	0.85[ASN][1000 genomes]
rs12054457	0.93[ASN][1000 genomes]
rs2031043	0.92[ASN][1000 genomes]
rs2031044	0.93[ASN][1000 genomes]
rs2056597	0.93[ASN][1000 genomes]
rs3774257	0.93[ASN][1000 genomes]
rs56383017	0.89[ASN][1000 genomes]
rs6764609	0.87[ASN][1000 genomes]
rs67667466	0.93[ASN][1000 genomes]
rs9817201	0.81[ASN][1000 genomes]
rs9822440	0.93[ASN][1000 genomes]
rs9841654	0.89[ASN][1000 genomes]
rs9871887	0.93[ASN][1000 genomes]
rs9875854	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829807	chr3:179527567-179745153	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv829808	chr3:179574614-179754321	Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv534210	chr3:179666123-179899347	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1000756	chr3:179672703-179827373	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr3:179689400-179710200	Weak transcription	Fetal Brain Male	brain
2	chr3:179692200-179694600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr3:179692200-179696200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr3:179692400-179692800	Enhancers	Brain Hippocampus Middle	brain
5	chr3:179692400-179695000	Weak transcription	Brain Angular Gyrus	brain
6	chr3:179692400-179695200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr3:179692400-179695200	Weak transcription	Brain Anterior Caudate	brain
8	chr3:179692400-179696600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr3:179692400-179696600	Weak transcription	Thymus	Thymus
10	chr3:179692400-179698200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:179692600-179693600	Weak transcription	Brain Substantia Nigra	brain
12	chr3:179692600-179694600	Weak transcription	Brain Cingulate Gyrus	brain
13	chr3:179692600-179695800	Enhancers	Dnd41	blood

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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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