Variant report

Variant	rs4655399
Chromosome Location	chr1:215419328-215419329
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10864165	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10864166	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10864169	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11120519	0.83[EUR][1000 genomes]
rs11120524	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11120530	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11120533	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11120539	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11120541	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11120542	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11583745	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11588455	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12026669	0.89[EUR][1000 genomes]
rs12026702	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12037855	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12044688	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12047082	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12049601	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12407482	0.87[EUR][1000 genomes]
rs12739619	0.85[EUR][1000 genomes]
rs12750276	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12752882	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1339401	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1416653	0.91[EUR][1000 genomes]
rs1416654	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1416655	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1416661	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1538544	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2153244	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3933352	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4098470	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4098471	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4655397	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4655398	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4655400	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6540886	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6540887	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6670661	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6674743	0.87[EUR][1000 genomes]
rs7522160	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7531046	0.91[EUR][1000 genomes]
rs946487	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs946488	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs946489	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs946490	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[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	nsv873169	chr1:215264486-215453286	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases
2	nsv873170	chr1:215367248-215440975	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215413400-215420200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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