Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11986591	0.87[ASN][1000 genomes]
rs12546847	0.96[ASN][1000 genomes]
rs12547891	0.92[ASN][1000 genomes]
rs12548164	0.97[ASN][1000 genomes]
rs13257117	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13261150	0.82[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs13261974	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13282499	0.85[ASN][1000 genomes]
rs1401862	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1879199	0.94[ASN][1000 genomes]
rs1915013	0.94[ASN][1000 genomes]
rs2030346	0.94[ASN][1000 genomes]
rs2139481	0.85[ASN][1000 genomes]
rs2139482	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2176771	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs28527305	0.92[ASN][1000 genomes]
rs28731145	0.93[ASN][1000 genomes]
rs28907588	0.83[ASN][1000 genomes]
rs4960952	0.94[ASN][1000 genomes]
rs4961080	0.81[ASN][1000 genomes]
rs6988189	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6990910	0.96[ASN][1000 genomes]
rs7001079	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7823166	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7835345	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9643051	0.95[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	nsv1029898	chr8:88837956-89606641	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1030028	chr8:89060085-89733470	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1019111	chr8:89186908-89475460	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89160800-89217200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:89177200-89214400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr8:89177200-89216400	Weak transcription	Brain Germinal Matrix	brain
4	chr8:89178000-89205200	Weak transcription	Fetal Stomach	stomach
5	chr8:89195000-89219200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr8:89195800-89210600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:89196600-89214200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr8:89196800-89214800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr8:89198800-89207000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr8:89200400-89206600	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr8:89201200-89218000	Weak transcription	Fetal Lung	lung
12	chr8:89202800-89204200	Enhancers	NH-A	brain
13	chr8:89203000-89204200	Enhancers	HUVEC	blood vessel
14	chr8:89203200-89211000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr8:89203400-89206400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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