Variant report

Variant	rs8128641
Chromosome Location	chr21:15602499-15602500
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs13048936	0.85[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs2041609	0.85[ASN][1000 genomes]
rs2080098	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2080099	0.86[ASN][1000 genomes]
rs2080100	0.92[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2098260	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2192165	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2245549	0.85[ASN][1000 genomes]
rs2245629	0.83[ASN][1000 genomes]
rs2245630	0.85[ASN][1000 genomes]
rs2245631	0.85[ASN][1000 genomes]
rs2403761	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822444	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2822446	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822447	0.92[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822452	0.91[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822454	0.91[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822457	0.91[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822478	0.86[ASN][1000 genomes]
rs2822479	0.84[ASN][1000 genomes]
rs2822480	0.86[ASN][1000 genomes]
rs2822481	0.86[ASN][1000 genomes]
rs2822482	0.86[ASN][1000 genomes]
rs2822483	0.85[ASN][1000 genomes]
rs2822485	0.85[ASN][1000 genomes]
rs2822486	0.85[ASN][1000 genomes]
rs2822487	0.85[ASN][1000 genomes]
rs2822488	0.85[ASN][1000 genomes]
rs2822489	0.85[ASN][1000 genomes]
rs2822491	0.85[ASN][1000 genomes]
rs2822493	0.85[ASN][1000 genomes]
rs2822494	0.85[ASN][1000 genomes]
rs2822495	0.85[ASN][1000 genomes]
rs2822496	0.85[ASN][1000 genomes]
rs2822497	0.85[ASN][1000 genomes]
rs2822498	0.85[ASN][1000 genomes]
rs2822499	0.85[ASN][1000 genomes]
rs2822500	0.85[ASN][1000 genomes]
rs2822501	0.85[ASN][1000 genomes]
rs2822502	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28450820	0.85[ASN][1000 genomes]
rs3937457	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4350835	0.85[ASN][1000 genomes]
rs4384867	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs4473468	0.85[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs7282747	0.86[ASN][1000 genomes]
rs8128704	0.91[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs9305261	0.86[ASN][1000 genomes]
rs9974101	0.85[ASN][1000 genomes]
rs9974145	0.84[ASN][1000 genomes]
rs9974227	0.91[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs9974337	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs9974434	0.91[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs9974778	0.84[ASN][1000 genomes]
rs9975653	0.86[ASN][1000 genomes]
rs9976642	0.86[ASN][1000 genomes]
rs9977630	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9978140	0.85[ASN][1000 genomes]
rs9978229	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9978235	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9978241	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9979382	0.85[ASN][1000 genomes]
rs9982191	0.92[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs9982795	0.92[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs9982809	0.85[ASN][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	nsv1058202	chr21:14706767-15628668	Weak transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
2	nsv869466	chr21:15482572-15683385	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv913402	chr21:15545350-15606128	Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv1056588	chr21:15583231-15615520	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1066738	chr21:15587815-15642948	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr21:15601000-15602600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr21:15602000-15603000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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