Variant report

Variant	rs752532
Chromosome Location	chr18:29587678-29587679
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs2059629	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57625132	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs59967923	0.87[EUR][1000 genomes]
rs7235750	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7236806	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73413942	0.85[EUR][1000 genomes]
rs8086283	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs8087275	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9948737	0.89[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065285	chr18:29527884-29614986	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29573600-29588400	Weak transcription	Right Atrium	heart
2	chr18:29586600-29588400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr18:29587000-29598000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr18:29587400-29588200	Enhancers	Liver	Liver
5	chr18:29587600-29588000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr18:29587600-29588200	Enhancers	Hela-S3	cervix

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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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