Variant report

Variant	rs34985833
Chromosome Location	chr3:179683537-179683538
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs13096827	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35040076	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35102009	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35362105	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62290481	0.86[AMR][1000 genomes];0.82[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:13 , 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	chr3:179679800-179688000	Weak transcription	Fetal Thymus	thymus
4	chr3:179680000-179684400	Enhancers	Brain Substantia Nigra	brain
5	chr3:179680600-179684200	Enhancers	Fetal Brain Female	brain
6	chr3:179681600-179684000	Weak transcription	GM12878-XiMat	blood
7	chr3:179682200-179686400	Enhancers	Brain Hippocampus Middle	brain
8	chr3:179682200-179688000	Weak transcription	Thymus	Thymus
9	chr3:179682400-179686800	Enhancers	Brain Cingulate Gyrus	brain
10	chr3:179682600-179683600	Enhancers	Brain Anterior Caudate	brain
11	chr3:179682800-179686800	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr3:179683200-179684000	Weak transcription	Brain Angular Gyrus	brain
13	chr3:179683200-179686400	Genic enhancers	Dnd41	blood

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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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