Variant report

Variant	rs2287224
Chromosome Location	chr3:179576819-179576820
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1567622	1.00[ASN][1000 genomes]
rs1567624	0.94[ASN][1000 genomes]
rs1609981	0.90[ASN][1000 genomes]
rs2037633	0.97[ASN][1000 genomes]
rs2177591	0.90[ASN][1000 genomes]
rs2879636	0.90[ASN][1000 genomes]
rs3774253	0.87[ASN][1000 genomes]
rs3821798	0.83[ASN][1000 genomes]
rs4146790	0.83[ASN][1000 genomes]
rs6443675	0.90[ASN][1000 genomes]
rs6784136	0.90[ASN][1000 genomes]
rs7616210	0.90[ASN][1000 genomes]
rs7634271	0.97[ASN][1000 genomes]
rs7650575	0.83[ASN][1000 genomes]
rs9836550	0.97[ASN][1000 genomes]
rs9862706	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	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

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179533800-179605000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr3:179537800-179599400	Weak transcription	Brain Anterior Caudate	brain
3	chr3:179554000-179590400	Weak transcription	Brain Substantia Nigra	brain
4	chr3:179559600-179589400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:179564200-179606000	Strong transcription	Dnd41	blood
6	chr3:179571400-179596800	Weak transcription	Brain Angular Gyrus	brain
7	chr3:179571800-179581200	Weak transcription	Right Atrium	heart
8	chr3:179575200-179591200	Weak transcription	Brain Hippocampus Middle	brain
9	chr3:179576200-179577000	Strong transcription	Brain Cingulate Gyrus	brain
10	chr3:179576200-179577000	Strong 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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