Variant report

Variant	rs57456024
Chromosome Location	chr8:58580573-58580574
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs11986045	0.91[EUR][1000 genomes]
rs16922305	0.83[EUR][1000 genomes]
rs16922371	0.91[EUR][1000 genomes]
rs16922399	0.91[EUR][1000 genomes]
rs28857234	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28894753	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36156385	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55718924	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56218904	0.83[EUR][1000 genomes]
rs56259251	0.83[EUR][1000 genomes]
rs57413963	0.91[EUR][1000 genomes]
rs58625384	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60023629	0.91[EUR][1000 genomes]
rs61193147	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6471633	0.91[EUR][1000 genomes]
rs6471634	0.91[EUR][1000 genomes]
rs6471635	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6989311	0.88[EUR][1000 genomes]
rs6992409	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6994367	0.88[EUR][1000 genomes]
rs6998927	0.88[EUR][1000 genomes]
rs7003082	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7005726	0.88[EUR][1000 genomes]
rs7007404	0.83[EUR][1000 genomes]
rs7009212	0.88[EUR][1000 genomes]
rs7009217	0.88[EUR][1000 genomes]
rs7012716	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72657140	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72657151	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72657154	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72657161	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72657163	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72657165	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72657168	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72657185	0.86[EUR][1000 genomes]
rs72657186	0.88[EUR][1000 genomes]
rs7814032	0.88[EUR][1000 genomes]
rs7821347	0.91[EUR][1000 genomes]
rs7822513	0.91[EUR][1000 genomes]
rs7825239	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7831758	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7838697	0.83[EUR][1000 genomes]
rs7842185	0.91[EUR][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	nsv533217	chr8:57991065-58789001	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58580200-58580600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:58580400-58581200	Enhancers	Fetal Stomach	stomach

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