Variant report

Variant	rs10184584
Chromosome Location	chr2:86818348-86818349
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:86817719..86819365-chr2:86821480..86823766,2	K562	blood:
2	chr2:86788344..86791163-chr2:86817304..86820517,4	MCF-7	breast:
3	chr2:86815800..86817434-chr2:86817538..86820109,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000115561	Chromatin interaction
ENSG00000228363	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10169746	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10184985	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10187753	0.99[ASN][1000 genomes]
rs10432704	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1080551	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11127047	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11689593	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12328637	0.83[ASN][1000 genomes]
rs12623509	0.83[ASN][1000 genomes]
rs12714190	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12714199	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2367546	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs308900	0.81[ASN][1000 genomes]
rs34666164	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs422240	0.81[ASN][1000 genomes]
rs4832043	0.82[ASN][1000 genomes]
rs4832302	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4832303	0.99[ASN][1000 genomes]
rs4832304	0.83[ASN][1000 genomes]
rs6733569	0.99[ASN][1000 genomes]
rs6752371	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7557796	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7568840	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7570640	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7584882	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7587034	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7601115	0.83[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	esv3412938	chr2:86370969-86867936	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
2	nsv532724	chr2:86622295-87086407	Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10184584	VPS24	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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