Variant report

Variant	rs57307831
Chromosome Location	chr8:20213989-20213990
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1038465	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10503678	0.80[AMR][1000 genomes]
rs12541289	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12542760	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12543131	0.80[AMR][1000 genomes]
rs12543855	0.80[AMR][1000 genomes]
rs12544394	0.80[AMR][1000 genomes]
rs12544659	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12679658	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13248765	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13249689	0.80[AMR][1000 genomes]
rs13256064	0.89[ASN][1000 genomes]
rs13276179	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13278066	0.80[AMR][1000 genomes]
rs13278974	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1484800	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2062348	0.80[AMR][1000 genomes]
rs34324466	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34368954	0.80[AMR][1000 genomes]
rs35102761	0.80[AMR][1000 genomes]
rs35851624	0.80[AMR][1000 genomes]
rs35946940	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4270981	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4376510	0.80[AMR][1000 genomes]
rs4397421	0.81[AMR][1000 genomes]
rs4397422	0.81[AMR][1000 genomes]
rs4451325	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4922167	0.80[AMR][1000 genomes]
rs4922168	0.80[AMR][1000 genomes]
rs4922171	0.80[AMR][1000 genomes]
rs4922172	0.80[AMR][1000 genomes]
rs57421611	0.80[AMR][1000 genomes]
rs58488103	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs66866121	0.80[AMR][1000 genomes]
rs754455	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs900956	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9325868	0.82[AMR][1000 genomes];0.87[EUR][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	nsv1033511	chr8:19751299-20625091	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv530877	chr8:19873053-20593254	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv831256	chr8:20162233-20300224	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20208400-20215600	Weak transcription	Fetal Brain Male	brain
2	chr8:20212600-20217400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:20213400-20214000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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