Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs12894998	0.96[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs177224	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs177226	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs177229	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs177238	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs177239	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs177243	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1955571	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3896379	0.82[ASN][1000 genomes]
rs4903678	0.80[ASN][1000 genomes]
rs4903686	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4903687	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4903688	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4903689	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6574416	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7140733	0.82[ASN][1000 genomes]
rs7146614	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7152858	0.92[ASN][1000 genomes]
rs7153421	0.96[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7160437	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs8019668	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs8021165	0.96[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs8022316	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757576	chr14:78379156-78502019	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv2759999	chr14:78379156-78502019	Genic enhancers Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv902108	chr14:78459047-78541015	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island 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	chr14:78496600-78499200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:78496800-78502200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:78499000-78500200	Enhancers	Brain Germinal Matrix	brain

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