Variant report

Variant	rs62255804
Chromosome Location	chr3:24149034-24149035
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:24146957..24149628-chr3:24155407..24157243,2	MCF-7	breast:
2	chr3:24142494..24143999-chr3:24147403..24150339,2	K562	blood:
3	chr3:24148783..24152054-chr3:24153553..24155525,3	K562	blood:

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

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

rs_ID	r²[population]
rs11129139	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12490512	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12491272	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12492765	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12498129	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4416338	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs55920816	0.86[EUR][1000 genomes]
rs57144868	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57903454	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs58523227	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs59374114	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs59461522	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59715267	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59911620	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs60635484	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs60706278	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62253424	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62253427	0.88[EUR][1000 genomes]
rs62255803	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6769284	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6769403	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6807599	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73134512	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7428009	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7623348	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7636932	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs826371	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs826372	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs826373	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs826374	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs826375	0.86[AMR][1000 genomes];0.94[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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:24143800-24160800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr3:24148200-24150000	Weak transcription	NHDF-Ad	bronchial
3	chr3:24148400-24163000	Weak transcription	Aorta	Aorta
4	chr3:24149000-24164000	Weak transcription	Left Ventricle	heart

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