Variant report

Variant	rs9289039
Chromosome Location	chr3:115767937-115767938
allele	C/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:26)

rs_ID	r²[population]
rs11918028	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12485818	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12495426	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13065579	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1920382	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1920383	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1920384	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1920385	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1920388	0.89[EUR][1000 genomes]
rs2141626	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2141627	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2141629	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4398428	0.85[EUR][1000 genomes]
rs6438296	0.86[EUR][1000 genomes]
rs6776244	0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6787687	0.87[EUR][1000 genomes]
rs6787872	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6795318	0.88[EUR][1000 genomes]
rs7610371	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7625191	0.89[EUR][1000 genomes]
rs7632252	0.89[EUR][1000 genomes]
rs9289040	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9845521	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9848298	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9863087	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9869887	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931948	chr3:114884574-115802562	Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	esv2760762	chr3:115476222-115807650	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv829685	chr3:115643521-115812913	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv1012260	chr3:115680931-115935968	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv2756413	chr3:115721898-115908480	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv1001538	chr3:115746561-115791116	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	esv2751975	chr3:115766285-115902901	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:115754000-115770400	Weak transcription	Brain Substantia Nigra	brain
2	chr3:115758000-115772800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:115758800-115769800	Weak transcription	NHEK	skin
4	chr3:115759000-115778200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:115762000-115769000	Weak transcription	Colon Smooth Muscle	Colon
6	chr3:115765400-115768000	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr3:115765800-115768000	Weak transcription	Fetal Muscle Leg	muscle
8	chr3:115765800-115768800	Weak transcription	K562	blood
9	chr3:115765800-115769600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr3:115765800-115770000	Weak transcription	Brain Cingulate Gyrus	brain
11	chr3:115765800-115770200	Weak transcription	Brain Anterior Caudate	brain
12	chr3:115765800-115770400	Weak transcription	Brain Hippocampus Middle	brain
13	chr3:115766000-115774000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr3:115766000-115775800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr3:115766200-115770000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr3:115766200-115770000	Weak transcription	Brain Angular Gyrus	brain
17	chr3:115766200-115770200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr3:115766200-115794200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr3:115767400-115768200	Enhancers	Fetal Lung	lung
20	chr3:115767600-115769000	Enhancers	Rectal Smooth Muscle	rectum
21	chr3:115767800-115768400	Enhancers	Fetal Stomach	stomach

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