Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1016589	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1474733	0.94[ASN][1000 genomes]
rs1474734	0.94[ASN][1000 genomes]
rs1540912	0.94[ASN][1000 genomes]
rs1540913	0.94[ASN][1000 genomes]
rs2092466	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2092467	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2143508	0.94[ASN][1000 genomes]
rs2206649	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2386706	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036744	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036746	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6036749	0.94[ASN][1000 genomes]
rs6036751	0.94[ASN][1000 genomes]
rs6049614	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049617	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049621	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049622	0.94[ASN][1000 genomes]
rs6049624	0.94[ASN][1000 genomes]
rs6049631	0.94[ASN][1000 genomes]
rs6083506	0.94[ASN][1000 genomes]
rs6114672	0.94[ASN][1000 genomes]
rs878289	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs926608	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv9793	chr20:23939613-24734850	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv833945	chr20:24163437-24349462	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1058146	chr20:24210196-24531087	Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv833946	chr20:24320375-24490702	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24332000-24341800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:24332600-24335000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr20:24333200-24337000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr20:24333200-24337600	Weak transcription	Brain Substantia Nigra	brain
5	chr20:24333400-24339400	Weak transcription	Brain Angular Gyrus	brain
6	chr20:24333800-24334600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr20:24334000-24338400	Enhancers	Brain Hippocampus Middle	brain
8	chr20:24334200-24334600	Enhancers	Dnd41	blood
9	chr20:24334400-24334800	Weak transcription	Brain Germinal Matrix	brain

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