Variant report

Variant	rs59193921
Chromosome Location	chr5:42363528-42363529
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10059747	0.91[EUR][1000 genomes]
rs10078935	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10472369	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11738203	1.00[EUR][1000 genomes]
rs11743641	0.89[EUR][1000 genomes]
rs11744988	0.91[EUR][1000 genomes]
rs11745718	0.94[EUR][1000 genomes]
rs11748224	0.94[EUR][1000 genomes]
rs11748684	0.91[EUR][1000 genomes]
rs28463913	0.96[EUR][1000 genomes]
rs56395635	1.00[EUR][1000 genomes]
rs56937761	0.98[EUR][1000 genomes]
rs57190315	0.87[EUR][1000 genomes]
rs57417495	1.00[EUR][1000 genomes]
rs58363453	0.91[EUR][1000 genomes]
rs66484535	0.90[EUR][1000 genomes]
rs66487711	0.98[EUR][1000 genomes]
rs66756362	0.98[EUR][1000 genomes]
rs67526935	0.94[EUR][1000 genomes]
rs67529954	0.98[EUR][1000 genomes]
rs67600650	0.98[EUR][1000 genomes]
rs6887313	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72750886	0.89[EUR][1000 genomes]
rs72750888	0.89[EUR][1000 genomes]
rs72750898	0.91[EUR][1000 genomes]
rs72750901	0.91[EUR][1000 genomes]
rs72753015	0.96[EUR][1000 genomes]
rs72753093	0.83[EUR][1000 genomes]
rs72753097	0.83[EUR][1000 genomes]
rs72753100	0.83[EUR][1000 genomes]
rs72754906	0.83[EUR][1000 genomes]
rs72754916	0.83[EUR][1000 genomes]
rs72754917	0.83[EUR][1000 genomes]
rs7710353	0.85[EUR][1000 genomes]
rs7714376	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7720893	0.85[EUR][1000 genomes]
rs7727915	0.81[AMR][1000 genomes];0.98[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	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
4	nsv881375	chr5:42254097-42442715	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv948514	chr5:42270161-42519262	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr5:42361400-42366800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr5:42361600-42366400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr5:42362200-42366200	Weak transcription	Muscle Satellite Cultured Cells	--

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