Variant report

Variant	rs7632865
Chromosome Location	chr3:146400961-146400962
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10935639	0.90[ASN][1000 genomes]
rs11709433	0.90[ASN][1000 genomes]
rs11709435	0.90[ASN][1000 genomes]
rs11713544	0.90[ASN][1000 genomes]
rs11718101	0.91[ASN][1000 genomes]
rs1511567	0.90[ASN][1000 genomes]
rs6767674	0.88[ASN][1000 genomes]
rs6804783	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv516386	chr3:146366513-146758405	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv4047	chr3:146368154-146401858	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv591961	chr3:146394094-146725217	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146398400-146404200	Enhancers	Dnd41	blood
2	chr3:146399200-146401000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:146400800-146401000	Enhancers	Brain Germinal Matrix	brain
4	chr3:146400800-146401000	Enhancers	Fetal Heart	heart

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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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