Variant report

Variant	rs9384474
Chromosome Location	chr6:150706613-150706614
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs11962096	0.88[ASN][1000 genomes]
rs11969964	0.82[ASN][1000 genomes]
rs12530375	0.89[ASN][1000 genomes]
rs1339104	0.82[ASN][1000 genomes]
rs1339105	0.82[ASN][1000 genomes]
rs1339106	0.82[ASN][1000 genomes]
rs1339107	0.82[ASN][1000 genomes]
rs1339110	0.85[ASN][1000 genomes]
rs1416481	0.84[ASN][1000 genomes]
rs1556881	0.98[ASN][1000 genomes]
rs1890522	1.00[CEU][hapmap]
rs2064213	0.81[ASN][1000 genomes]
rs2076285	0.88[ASN][1000 genomes]
rs2076286	0.88[ASN][1000 genomes]
rs2076287	0.98[ASN][1000 genomes]
rs2076288	0.98[ASN][1000 genomes]
rs2076289	0.98[ASN][1000 genomes]
rs2076290	0.98[ASN][1000 genomes]
rs2076291	0.98[ASN][1000 genomes]
rs2076292	0.98[ASN][1000 genomes]
rs3734734	0.98[ASN][1000 genomes]
rs3823259	0.93[ASN][1000 genomes]
rs3823260	0.94[ASN][1000 genomes]
rs4407723	0.97[ASN][1000 genomes]
rs4478415	1.00[CEU][hapmap]
rs61253143	0.81[ASN][1000 genomes]
rs62432482	0.82[ASN][1000 genomes]
rs62432483	0.85[ASN][1000 genomes]
rs62432484	0.86[ASN][1000 genomes]
rs62432506	0.96[ASN][1000 genomes]
rs62432511	0.98[ASN][1000 genomes]
rs62432540	0.88[ASN][1000 genomes]
rs62432541	0.88[ASN][1000 genomes]
rs62432542	0.88[ASN][1000 genomes]
rs6909655	0.88[ASN][1000 genomes]
rs6921360	0.88[ASN][1000 genomes]
rs73617698	0.94[ASN][1000 genomes]
rs7745569	0.97[ASN][1000 genomes]
rs7761373	0.82[ASN][1000 genomes]
rs7761906	0.97[ASN][1000 genomes]
rs7762616	0.89[ASN][1000 genomes]
rs7769542	0.82[ASN][1000 genomes]
rs7770389	1.00[ASN][1000 genomes]
rs7774077	0.93[ASN][1000 genomes]
rs7774404	0.85[ASN][1000 genomes]
rs9322259	0.98[ASN][1000 genomes]
rs9371429	0.85[ASN][1000 genomes]
rs9371437	0.98[ASN][1000 genomes]
rs9383808	0.97[ASN][1000 genomes]
rs9384388	1.00[CEU][hapmap]
rs9384472	0.98[ASN][1000 genomes]
rs9384473	1.00[ASN][1000 genomes]
rs9384476	0.98[ASN][1000 genomes]
rs9397302	0.98[ASN][1000 genomes]
rs9397303	0.98[ASN][1000 genomes]
rs9397944	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	esv2763602	chr6:150581193-150720666	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150706200-150711800	Weak transcription	Fetal Intestine Small	intestine

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