Variant report

Variant	rs7848774
Chromosome Location	chr9:85832774-85832775
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10867954	0.88[GIH][hapmap]
rs11139954	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11139955	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11139959	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11139965	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11139971	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11139973	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11139975	0.94[CEU][hapmap];0.85[CHD][hapmap];0.96[TSI][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11139976	0.85[MEX][hapmap]
rs11139978	0.91[GIH][hapmap]
rs11139983	0.91[GIH][hapmap]
rs1323772	0.94[CEU][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1408102	0.86[GIH][hapmap]
rs17400361	0.94[CEU][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4877745	0.85[GIH][hapmap]
rs58862231	0.99[AMR][1000 genomes];0.93[EUR][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	nsv893511	chr9:85495968-85833127	Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr9:85824200-85834200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr9:85827800-85833800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr9:85832000-85833600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:85832000-85834200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:85832000-85834200	Weak transcription	Gastric	stomach

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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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