Variant report

Variant	rs7618832
Chromosome Location	chr3:160488395-160488396
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10513553	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12486979	0.82[EUR][1000 genomes]
rs12487861	0.83[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap]
rs12494732	0.80[JPT][hapmap]
rs13068380	0.89[EUR][1000 genomes]
rs1378654	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1378657	1.00[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1378658	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1403048	0.82[EUR][1000 genomes]
rs1455869	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap];0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1598495	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16831457	0.81[YRI][hapmap]
rs1829716	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1839019	0.80[JPT][hapmap]
rs1851378	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[YRI][hapmap];0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1902282	0.82[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.89[ASN][1000 genomes]
rs1915929	0.86[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs2049214	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2049215	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2886905	0.83[EUR][1000 genomes]
rs4256178	0.80[JPT][hapmap]
rs59542611	0.90[EUR][1000 genomes]
rs6775743	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap]
rs6781371	0.81[EUR][1000 genomes]
rs6794047	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6805905	0.83[EUR][1000 genomes]
rs718757	1.00[CEU][hapmap];0.96[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap];0.90[EUR][1000 genomes]
rs722871	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7630250	0.89[ASN][1000 genomes]
rs7634342	0.83[EUR][1000 genomes]
rs7640348	0.81[EUR][1000 genomes]
rs7642371	0.83[EUR][1000 genomes]
rs7643513	0.82[EUR][1000 genomes]
rs779058	0.89[ASN][1000 genomes]
rs972909	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9809208	0.80[JPT][hapmap]
rs9810290	0.80[JPT][hapmap]
rs9814394	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9815499	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9833075	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9866566	1.00[CEU][hapmap];0.96[CHB][hapmap];0.95[JPT][hapmap];0.97[YRI][hapmap];0.90[EUR][1000 genomes]
rs9868489	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160475800-160497200	Weak transcription	Left Ventricle	heart
2	chr3:160476000-160496400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr3:160477400-160489600	Weak transcription	Fetal Heart	heart
4	chr3:160477600-160489800	Weak transcription	Brain Anterior Caudate	brain
5	chr3:160477600-160497000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:160477600-160498200	Weak transcription	Stomach Mucosa	stomach
7	chr3:160477800-160497800	Weak transcription	Brain Angular Gyrus	brain
8	chr3:160483400-160489800	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr3:160483800-160488400	Weak transcription	Stomach Smooth Muscle	stomach
10	chr3:160483800-160489400	Weak transcription	Colon Smooth Muscle	Colon
11	chr3:160484400-160496600	Weak transcription	Primary T cells from cord blood	blood
12	chr3:160487000-160488400	Weak transcription	Psoas Muscle	Psoas
13	chr3:160487200-160490000	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr3:160487200-160502200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:160487600-160488400	Enhancers	HUVEC	blood vessel
16	chr3:160488000-160489400	Weak transcription	Rectal Smooth Muscle	rectum
17	chr3:160488200-160488600	Enhancers	Pancreatic Islets	Pancreatic Islet

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