Variant report

Variant	rs35040076
Chromosome Location	chr3:179681551-179681552
allele	C/T
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:11)

rs_ID	r²[population]
rs11917103	0.81[EUR][1000 genomes]
rs11923858	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13096827	0.96[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17749273	0.82[EUR][1000 genomes]
rs34985833	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35068209	0.82[EUR][1000 genomes]
rs35102009	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35362105	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62290481	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6795496	0.81[EUR][1000 genomes]
rs6807998	0.81[EUR][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:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179675800-179688000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr3:179677200-179685000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:179678800-179682000	Weak transcription	Brain Anterior Caudate	brain
4	chr3:179679800-179688000	Weak transcription	Fetal Thymus	thymus
5	chr3:179680000-179684400	Enhancers	Brain Substantia Nigra	brain
6	chr3:179680400-179681600	Enhancers	GM12878-XiMat	blood
7	chr3:179680600-179682000	Enhancers	Dnd41	blood
8	chr3:179680600-179684200	Enhancers	Fetal Brain Female	brain
9	chr3:179680800-179681600	Enhancers	Pancreas	Pancrea
10	chr3:179681000-179682200	Weak transcription	Brain Hippocampus Middle	brain
11	chr3:179681000-179682600	Enhancers	Brain Angular Gyrus	brain
12	chr3:179681200-179682000	Weak transcription	Thymus	Thymus
13	chr3:179681400-179682400	Weak transcription	Brain Cingulate Gyrus	brain
14	chr3:179681400-179682800	Weak transcription	Brain Inferior Temporal Lobe	brain

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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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