Variant report

Variant	rs8027255
Chromosome Location	chr15:73754380-73754381
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:73752556..73755114-chr15:73923552..73926057,2	K562	blood:

Variant related genes	Relation type
ENSG00000156642	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10162605	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10163172	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11638472	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11854774	0.82[EUR][1000 genomes]
rs11856313	0.82[EUR][1000 genomes]
rs12324832	0.82[EUR][1000 genomes]
rs12908815	0.96[EUR][1000 genomes]
rs13380155	0.95[EUR][1000 genomes]
rs13380245	0.96[EUR][1000 genomes]
rs1481087	0.80[EUR][1000 genomes]
rs1582742	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16957919	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16957997	0.82[EUR][1000 genomes]
rs16958019	0.82[EUR][1000 genomes]
rs16958025	0.82[EUR][1000 genomes]
rs16958041	0.80[EUR][1000 genomes]
rs16958050	0.82[EUR][1000 genomes]
rs2306462	0.82[EUR][1000 genomes]
rs2415153	0.82[EUR][1000 genomes]
rs28834466	0.82[EUR][1000 genomes]
rs3889590	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55636021	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55695286	0.96[EUR][1000 genomes]
rs56190024	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56227598	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57995256	0.82[EUR][1000 genomes]
rs60419012	0.82[EUR][1000 genomes]
rs6495066	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7163212	0.82[EUR][1000 genomes]
rs7163693	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7164953	0.82[EUR][1000 genomes]
rs7165447	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7166673	0.82[EUR][1000 genomes]
rs7169976	0.96[EUR][1000 genomes]
rs7172130	0.89[EUR][1000 genomes]
rs7172448	0.85[EUR][1000 genomes]
rs7173068	1.00[EUR][1000 genomes]
rs7176452	0.80[EUR][1000 genomes]
rs7177731	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7178806	0.82[EUR][1000 genomes]
rs729155	0.80[EUR][1000 genomes]
rs8028749	0.82[EUR][1000 genomes]
rs8033242	0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8036438	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8039862	0.80[EUR][1000 genomes]
rs8040552	0.98[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	nsv904343	chr15:73396760-73775043	Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv1037540	chr15:73712637-73982420	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats 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	34 gene(s)	inside rSNPs	diseases

No data

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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