Variant report

Variant	rs897494
Chromosome Location	chr3:160529290-160529291
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12486979	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12637922	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13073659	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1378654	0.83[EUR][1000 genomes]
rs1378655	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1378656	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1378657	0.83[EUR][1000 genomes]
rs1378660	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1403048	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1851378	0.80[EUR][1000 genomes]
rs2049214	0.81[EUR][1000 genomes]
rs2049215	0.81[EUR][1000 genomes]
rs2886905	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2886909	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6441331	0.82[AMR][1000 genomes]
rs6781371	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6794047	0.81[EUR][1000 genomes]
rs6805905	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7633816	0.82[AMR][1000 genomes]
rs7634342	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7640231	0.81[EUR][1000 genomes]
rs7640348	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7642371	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7643513	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs959960	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs972909	0.81[EUR][1000 genomes]
rs9809208	0.82[AFR][1000 genomes]
rs9833075	0.83[EUR][1000 genomes]
rs9883862	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv532666	chr3:159777847-160703202	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv1009249	chr3:160496237-160627378	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv536780	chr3:160496237-160627378	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160520400-160529600	Weak transcription	Colonic Mucosa	Colon
2	chr3:160523000-160532800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr3:160525800-160530200	Enhancers	Adipose Nuclei	Adipose
4	chr3:160525800-160530400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr3:160525800-160530600	Enhancers	Fetal Brain Female	brain
6	chr3:160525800-160530800	Enhancers	Fetal Brain Male	brain
7	chr3:160526000-160530200	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr3:160526000-160530600	Enhancers	Colon Smooth Muscle	Colon
9	chr3:160526400-160530600	Enhancers	Brain Anterior Caudate	brain
10	chr3:160526600-160529800	Enhancers	NHDF-Ad	bronchial
11	chr3:160526600-160530400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr3:160526600-160530400	Weak transcription	Fetal Heart	heart
13	chr3:160526800-160529800	Weak transcription	Gastric	stomach
14	chr3:160527400-160530600	Enhancers	Stomach Smooth Muscle	stomach
15	chr3:160527600-160529600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr3:160527600-160529600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr3:160527800-160530600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr3:160528000-160529600	Weak transcription	Psoas Muscle	Psoas
19	chr3:160528200-160529600	Weak transcription	Right Atrium	heart
20	chr3:160528200-160530200	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr3:160528200-160537600	Weak transcription	Hela-S3	cervix
22	chr3:160528400-160529600	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr3:160528400-160529600	Weak transcription	Left Ventricle	heart
24	chr3:160528400-160533000	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr3:160528600-160529600	Weak transcription	Brain Substantia Nigra	brain
26	chr3:160528600-160530200	Weak transcription	Right Ventricle	heart
27	chr3:160528600-160530400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr3:160528600-160530800	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr3:160528800-160529600	Weak transcription	Brain Angular Gyrus	brain
30	chr3:160529000-160529800	Weak transcription	Brain Hippocampus Middle	brain
31	chr3:160529000-160530000	Weak transcription	Brain Cingulate Gyrus	brain
32	chr3:160529000-160530200	Weak transcription	Brain Germinal Matrix	brain
33	chr3:160529000-160530600	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr3:160529000-160534400	Weak transcription	Aorta	Aorta
35	chr3:160529200-160529800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr3:160529200-160530600	Enhancers	Fetal Muscle Leg	muscle
37	chr3:160529200-160533800	Weak transcription	Rectal Smooth Muscle	rectum

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