Variant report

Variant	rs57190315
Chromosome Location	chr5:42237846-42237847
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10059747	0.87[EUR][1000 genomes]
rs10078935	0.83[EUR][1000 genomes]
rs10472369	0.83[EUR][1000 genomes]
rs11738203	0.87[EUR][1000 genomes]
rs11744111	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11745718	0.82[EUR][1000 genomes]
rs11748684	0.87[EUR][1000 genomes]
rs28463913	0.83[EUR][1000 genomes]
rs4626371	0.89[EUR][1000 genomes]
rs56395635	0.87[EUR][1000 genomes]
rs56937761	0.85[EUR][1000 genomes]
rs57417495	0.87[EUR][1000 genomes]
rs59193921	0.87[EUR][1000 genomes]
rs632207	0.87[EUR][1000 genomes]
rs666581	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs66756362	0.85[EUR][1000 genomes]
rs6887313	0.87[EUR][1000 genomes]
rs72748687	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72748699	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72750866	0.85[EUR][1000 genomes]
rs72750886	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72750888	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72750898	0.87[EUR][1000 genomes]
rs72750901	0.87[EUR][1000 genomes]
rs72753015	0.83[EUR][1000 genomes]
rs7710353	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7714376	0.83[EUR][1000 genomes]
rs7720893	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7727915	0.85[EUR][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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42237400-42238000	Weak transcription	Adipose Nuclei	Adipose
2	chr5:42237600-42242000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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