Variant report

Variant	rs1016589
Chromosome Location	chr20:24344702-24344703
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1474733	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1474734	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1474735	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1540912	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1540913	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2092466	0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2092467	0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2143508	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2206649	0.87[AMR][1000 genomes]
rs2386706	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6036744	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6036746	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036747	0.83[AMR][1000 genomes]
rs6036748	0.84[AMR][1000 genomes]
rs6036749	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6036751	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6036753	0.82[AMR][1000 genomes]
rs6049614	0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6049617	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6049620	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6049621	0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6049622	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6049623	0.83[AMR][1000 genomes]
rs6049624	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6049631	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6083506	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6114672	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs878289	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs926608	0.87[AMR][1000 genomes];0.94[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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24343800-24346000	Enhancers	Dnd41	blood
2	chr20:24344400-24344800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr20:24344600-24346000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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