Variant report

Variant	rs9311768
Chromosome Location	chr3:60638709-60638710
allele	A/C/G/T
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:7)

rs_ID	r²[population]
rs13063937	1.00[JPT][hapmap]
rs4974239	1.00[JPT][hapmap]
rs4974255	1.00[JPT][hapmap]
rs6802326	1.00[JPT][hapmap]
rs9311769	0.83[YRI][hapmap];0.83[AFR][1000 genomes]
rs9311771	0.85[AFR][1000 genomes]
rs9827764	0.80[YRI][hapmap]

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	nsv529602	chr3:60088353-60830769	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv998815	chr3:60495872-60830769	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv999828	chr3:60537384-60785274	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60630800-60639400	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr3:60637800-60639600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr3:60638000-60638800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr3:60638000-60639400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr3:60638000-60644400	Weak transcription	H1 Cell Line	embryonic stem cell

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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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