Variant report

Variant	rs4762934
Chromosome Location	chr12:20355013-20355014
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1030460	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10734698	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10770619	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1160229	0.93[EUR][1000 genomes]
rs11610286	0.95[ASN][1000 genomes]
rs11610290	0.95[ASN][1000 genomes]
rs11831329	0.97[ASN][1000 genomes]
rs12815060	0.95[ASN][1000 genomes]
rs1427995	0.81[AMR][1000 genomes]
rs35148005	0.95[ASN][1000 genomes]
rs4762935	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56317263	0.95[ASN][1000 genomes]
rs6487065	0.85[EUR][1000 genomes]
rs7297897	0.84[EUR][1000 genomes]
rs7308275	0.84[EUR][1000 genomes]
rs7312491	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs763488	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7970503	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7979819	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[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	nsv1035141	chr12:20286595-20429040	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv557700	chr12:20346383-20379710	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv527363	chr12:20354786-20355013	Strong transcription Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4762934	AEBP2	cis	parietal	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20354200-20355200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr12:20354200-20356000	Strong transcription	Aorta	Aorta
3	chr12:20354600-20355800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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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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