Variant report

Variant	rs7786896
Chromosome Location	chr7:39093928-39093929
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11761423	0.88[CHB][hapmap];0.84[CHD][hapmap]
rs11769233	0.88[CHB][hapmap];0.83[CHD][hapmap]
rs1405000	0.89[CHB][hapmap];0.84[CHD][hapmap]
rs17255994	1.00[JPT][hapmap]
rs62442180	0.98[ASN][1000 genomes]
rs6462889	0.92[CEU][hapmap];0.89[CHB][hapmap];0.86[EUR][1000 genomes]
rs6462890	0.86[EUR][1000 genomes]
rs6959715	0.89[CHB][hapmap]
rs723969	1.00[JPT][hapmap]
rs73120491	0.98[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	nsv1024142	chr7:38978728-39300444	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	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	chr7:39082400-39094000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:39091800-39097800	Weak transcription	Aorta	Aorta
3	chr7:39092400-39094000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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