Variant report

Variant	rs9472484
Chromosome Location	chr6:12758212-12758213
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1011188	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10434855	0.89[EUR][1000 genomes]
rs10498681	0.98[EUR][1000 genomes]
rs12525116	0.98[EUR][1000 genomes]
rs12525210	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12526812	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12528247	0.93[EUR][1000 genomes]
rs12528721	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1571996	0.89[EUR][1000 genomes]
rs1572001	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17616767	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17617491	0.89[EUR][1000 genomes]
rs17678734	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17679286	0.89[EUR][1000 genomes]
rs2015761	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2151221	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2876298	0.98[EUR][1000 genomes]
rs35278288	0.89[EUR][1000 genomes]
rs4285318	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4293998	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4577783	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4583985	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4711817	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4714931	0.89[EUR][1000 genomes]
rs55764622	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs55879442	0.93[EUR][1000 genomes]
rs56244510	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56259669	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56270763	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs58666803	0.85[EUR][1000 genomes]
rs60954427	0.85[EUR][1000 genomes]
rs6915585	0.89[EUR][1000 genomes]
rs73722820	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73722822	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73722823	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73722845	0.93[EUR][1000 genomes]
rs73722849	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7768030	0.89[EUR][1000 genomes]
rs9369607	0.89[EUR][1000 genomes]
rs9369612	0.89[EUR][1000 genomes]
rs9381451	0.85[EUR][1000 genomes]
rs9463091	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9463093	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9463105	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9463114	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9463117	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9463119	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9463140	0.98[EUR][1000 genomes]
rs9472511	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9472512	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9472513	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9472514	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9472519	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9472520	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9472528	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9472549	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9472566	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs950719	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3521000	chr6:12561306-13128519	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3521001	chr6:12561306-13128519	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	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	chr6:12752600-12767200	Weak transcription	Fetal Brain Male	brain

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