Variant report

Variant	rs58457553
Chromosome Location	chr2:134505193-134505194
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10496709	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12464809	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12465737	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12466546	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12467346	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12472423	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12475377	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13014446	0.82[ASN][1000 genomes]
rs1446748	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1446749	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1470510	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1562349	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16828705	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16828728	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17767728	0.85[ASN][1000 genomes]
rs17768541	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17819620	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1867894	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1992783	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1992784	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34163450	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35593895	0.91[ASN][1000 genomes]
rs4369917	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4369918	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55715603	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55787899	0.91[ASN][1000 genomes]
rs55932202	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56111185	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56160327	0.91[ASN][1000 genomes]
rs56341649	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6706052	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72843241	0.84[ASN][1000 genomes]
rs72843245	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72843247	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72843252	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72843260	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72843263	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72843280	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs921087	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003624	chr2:134126928-134583203	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1006101	chr2:134263288-134973917	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1013713	chr2:134322236-134644574	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv535931	chr2:134322236-134644574	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:134503600-134505400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr2:134503600-134506600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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