Variant report

Variant	rs35456562
Chromosome Location	chr2:115487203-115487204
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:115486382..115487273-chr2:115940531..115941348,2	MCF-7	breast:
2	chr2:115486408..115487261-chr2:115951872..115952594,3	MCF-7	breast:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1002872	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10203323	1.00[ASN][1000 genomes]
rs10211528	1.00[ASN][1000 genomes]
rs12463387	0.86[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12463533	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12478020	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12711803	1.00[ASN][1000 genomes]
rs13010772	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13017277	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13022000	1.00[ASN][1000 genomes]
rs13032093	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13386918	1.00[ASN][1000 genomes]
rs13425488	1.00[ASN][1000 genomes]
rs13430153	1.00[ASN][1000 genomes]
rs17043351	0.86[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17043357	0.90[AFR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17043364	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17729212	1.00[ASN][1000 genomes]
rs17729314	1.00[ASN][1000 genomes]
rs17730230	1.00[ASN][1000 genomes]
rs17786067	1.00[ASN][1000 genomes]
rs4569486	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71418511	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71418512	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71418517	1.00[ASN][1000 genomes]
rs72955668	1.00[ASN][1000 genomes]
rs7605779	1.00[ASN][1000 genomes]
rs930314	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs967034	1.00[ASN][1000 genomes]

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	nsv874904	chr2:114751691-115605062	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv431502	chr2:115139566-115617936	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv431524	chr2:115425650-115530770	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:115486600-115487400	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr2:115486600-115487400	Enhancers	Brain Hippocampus Middle	brain
3	chr2:115486600-115487600	Enhancers	Brain Anterior Caudate	brain
4	chr2:115486800-115487400	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr2:115487200-115488000	Enhancers	Brain Angular Gyrus	brain

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