Variant report

Variant	rs9840064
Chromosome Location	chr3:118999338-118999339
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs13315549	0.86[MEX][hapmap];0.87[TSI][hapmap]
rs2594731	0.86[MEX][hapmap];0.87[TSI][hapmap]
rs4234656	0.87[TSI][hapmap]
rs6766503	0.86[MEX][hapmap];0.87[TSI][hapmap]
rs6805930	0.86[MEX][hapmap];0.87[TSI][hapmap]
rs7613994	1.00[ASW][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	esv3487859	chr3:118570588-119419623	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv3487860	chr3:118570588-119419623	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	esv18354	chr3:118855337-119000251	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 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	chr3:118997400-118999400	Enhancers	HUVEC	blood vessel
2	chr3:118998600-119001200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:118998600-119001400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr3:118998800-119000200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr3:118999000-119000200	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr3:118999000-119001200	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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