Variant report

Variant	rs2099520
Chromosome Location	chr8:58795242-58795243
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10504248	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1112530	1.00[JPT][hapmap]
rs13273087	0.82[AFR][1000 genomes]
rs1369771	1.00[ASN][1000 genomes]
rs1369772	1.00[ASN][1000 genomes]
rs1436018	1.00[ASN][1000 genomes]
rs16918685	1.00[ASN][1000 genomes]
rs16922716	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2082912	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs55774155	1.00[ASN][1000 genomes]
rs58879638	1.00[ASN][1000 genomes]
rs6471659	1.00[ASN][1000 genomes]
rs6992698	1.00[ASN][1000 genomes]
rs73680595	1.00[ASN][1000 genomes]
rs73683803	1.00[ASN][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	nsv831323	chr8:58692548-58849862	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58789200-58804000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr8:58790800-58796000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:58795200-58797200	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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