Variant report

Variant	rs12588715
Chromosome Location	chr14:56341298-56341299
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs12588231	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12589557	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12590605	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12590983	0.82[ASN][1000 genomes]
rs12878170	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12886283	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12886883	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12887415	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12888134	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12891989	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12892029	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12892971	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12896271	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17128832	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17128836	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17128847	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17128862	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17128871	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17128875	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17128879	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17128880	0.80[ASN][1000 genomes]
rs1953361	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2095490	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34130924	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34181761	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34190854	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34403994	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34749214	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34831029	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34973073	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35177157	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35201150	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35361184	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35604109	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35657227	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35787613	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35847182	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35874101	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35969016	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs57997565	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs71412699	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7144347	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7149370	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7154675	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7158865	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7161015	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8019004	0.82[ASN][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	nsv901966	chr14:56160904-56436203	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv901977	chr14:56213392-56492996	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56339600-56341600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:56339600-56348600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:56340200-56341600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr14:56340400-56341600	Weak transcription	Brain Hippocampus Middle	brain

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