Variant report

Variant	rs348493
Chromosome Location	chr4:45185773-45185774
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10001028	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11725284	0.94[EUR][1000 genomes]
rs11737058	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12503507	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13103657	0.94[EUR][1000 genomes]
rs1355611	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1398266	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1512302	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1512308	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1512323	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1581096	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16857979	0.94[EUR][1000 genomes]
rs1828600	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1828601	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1828602	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1913019	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs348494	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs348496	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4295304	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6414674	0.94[EUR][1000 genomes]
rs6831362	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6844273	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7660147	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7670865	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7680194	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7685861	0.94[EUR][1000 genomes]
rs7687383	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs963316	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs979578	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs979580	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs986722	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs996004	0.94[EUR][1000 genomes]
rs9996542	0.90[AMR][1000 genomes];0.94[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	nsv531944	chr4:44299343-45200700	Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1014327	chr4:44735209-45218149	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv829919	chr4:45069901-45253808	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv594104	chr4:45105210-45665828	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv461349	chr4:45175691-45265046	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv594105	chr4:45175691-45265046	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:45185400-45185800	Enhancers	Adipose Nuclei	Adipose
2	chr4:45185400-45186200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr4:45185400-45192200	Weak transcription	Fetal Heart	heart
4	chr4:45185600-45186400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr4:45185600-45186800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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