Variant report

Variant	rs7651805
Chromosome Location	chr3:179673117-179673118
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1474366	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1474367	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1524512	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1524513	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2140655	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2177590	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs57784912	0.80[EUR][1000 genomes]
rs62290486	0.80[EUR][1000 genomes]
rs6443683	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6762528	0.82[EUR][1000 genomes]
rs6769137	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6804380	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6804648	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7610053	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7612374	0.80[EUR][1000 genomes]
rs7619212	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7642043	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7642245	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7642327	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7645533	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9290686	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9832433	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9842358	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9856937	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9862738	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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
5	esv3359522	chr3:179672744-179673221	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179660600-179680800	Weak transcription	Pancreas	Pancrea
2	chr3:179668000-179675200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr3:179671400-179673200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:179671400-179673200	Flanking Active TSS	Dnd41	blood
5	chr3:179671400-179674600	Enhancers	Fetal Thymus	thymus
6	chr3:179671800-179676400	Enhancers	Brain Cingulate Gyrus	brain
7	chr3:179672200-179674400	Enhancers	Thymus	Thymus
8	chr3:179672200-179676000	Weak transcription	Brain Anterior Caudate	brain
9	chr3:179672200-179679600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr3:179672400-179673800	Weak transcription	Brain Substantia Nigra	brain
11	chr3:179672800-179674400	Weak transcription	Brain Angular Gyrus	brain
12	chr3:179672800-179674400	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr3:179672800-179674800	Weak transcription	Brain Hippocampus Middle	brain

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