Variant report

Variant	rs2875697
Chromosome Location	chr8:58281800-58281801
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs2325660	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2325741	0.83[EUR][1000 genomes]
rs2875734	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4268115	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4304319	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4310195	0.83[EUR][1000 genomes]
rs4391420	0.84[EUR][1000 genomes]
rs4552888	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4633050	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4634626	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6651274	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6651294	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6651295	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7459901	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7817684	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7827445	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7829313	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758161	chr8:57930392-58474449	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv2759618	chr8:57930392-58474449	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv533217	chr8:57991065-58789001	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv890936	chr8:58266339-58564501	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 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	chr8:58280600-58283200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
2	chr8:58280800-58282200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
3	chr8:58281400-58281800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:58281600-58284400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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