Variant report

Variant	rs55706441
Chromosome Location	chr12:26086717-26086718
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs12322003	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1390324	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16929602	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16929615	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16929655	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16929667	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16929669	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16929681	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2054889	0.83[EUR][1000 genomes]
rs2643931	0.81[AMR][1000 genomes]
rs4485193	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4963930	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4963931	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4963932	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4963933	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4963935	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55920249	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57563237	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73073022	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73074805	0.99[EUR][1000 genomes]
rs73074809	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73074810	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73074813	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73074823	0.99[EUR][1000 genomes]
rs73088141	0.94[EUR][1000 genomes]
rs73088153	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73088155	0.95[EUR][1000 genomes]
rs73088172	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73292753	0.86[AMR][1000 genomes]
rs829830	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758300	chr12:25992331-26161116	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
2	esv2759886	chr12:25992331-26161116	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
3	nsv1035319	chr12:26020667-26097148	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA miRNA	6 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	chr12:26085400-26110600	Weak transcription	Aorta	Aorta
2	chr12:26086200-26086800	Enhancers	NHDF-Ad	bronchial
3	chr12:26086400-26086800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:26086400-26086800	Enhancers	Ovary	ovary

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