Variant report

Variant	rs57144868
Chromosome Location	chr3:24144965-24144966
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11129139	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12490512	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12491272	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12492765	0.85[EUR][1000 genomes]
rs12498129	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4416338	0.85[EUR][1000 genomes]
rs55920816	0.85[EUR][1000 genomes]
rs57903454	0.86[EUR][1000 genomes]
rs58523227	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59374114	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59461522	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs59715267	0.86[EUR][1000 genomes]
rs59911620	0.86[EUR][1000 genomes]
rs60635484	0.86[EUR][1000 genomes]
rs60706278	0.87[EUR][1000 genomes]
rs62253424	0.85[EUR][1000 genomes]
rs62253427	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62255803	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62255804	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6769284	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6769403	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6807599	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73134512	0.84[EUR][1000 genomes]
rs7428009	0.86[EUR][1000 genomes]
rs7623348	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7636932	0.86[EUR][1000 genomes]
rs826371	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs826372	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs826373	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs826374	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs826375	0.86[AMR][1000 genomes];0.92[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	nsv533980	chr3:23445901-24311972	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv834639	chr3:24037113-24233925	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 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	chr3:24143800-24160800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr3:24144000-24145200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:24144400-24147400	Weak transcription	NHDF-Ad	bronchial

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