Variant report

Variant	rs73090168
Chromosome Location	chr5:42243802-42243803
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10038605	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs10055579	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs10061546	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs10065700	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs10075533	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs10077196	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs13355247	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs13356114	0.81[AFR][1000 genomes]
rs13357631	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs28530765	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6886712	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73090140	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73090159	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7732413	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7732650	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7737752	0.83[AFR][1000 genomes]
rs9292847	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933208	chr5:41879946-42876624	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	112 gene(s)	inside rSNPs	diseases
2	nsv492147	chr5:41902086-42896162	Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	113 gene(s)	inside rSNPs	diseases
3	nsv1034208	chr5:42119128-42290759	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	esv1825573	chr5:42229421-42306381	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv880518	chr5:42231896-42375243	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42242400-42244200	Enhancers	Adipose Nuclei	Adipose
2	chr5:42243800-42244000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:42243800-42244600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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