Variant report

Variant	rs9885349
Chromosome Location	chr5:119301867-119301868
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10039840	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10519619	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11742877	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12173248	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12659053	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13354856	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1373322	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17145950	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17145954	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2130733	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4073706	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4073707	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4639259	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4895213	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4895214	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55700824	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs55927647	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs55992493	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56279521	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs56339003	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56361151	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs57621848	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs57903181	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs59277139	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62375599	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62375600	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6865691	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6874179	0.86[AMR][1000 genomes]
rs6877373	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6884836	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs720649	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72794430	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7712290	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9654530	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024455	chr5:118770429-119487982	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1016271	chr5:118836891-119487982	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv882778	chr5:118972113-119384039	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv599568	chr5:119199265-119414589	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	esv1833699	chr5:119233362-119304651	Weak transcription Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv968114	chr5:119301753-119302754	Enhancers	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119301200-119302400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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