Variant report

Variant	rs712586
Chromosome Location	chr5:115653900-115653901
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10051539	0.84[CEU][hapmap];0.80[CHB][hapmap];0.86[JPT][hapmap]
rs10055039	0.92[CEU][hapmap];0.89[CHB][hapmap];0.82[JPT][hapmap]
rs10072430	0.93[CEU][hapmap];0.85[CHB][hapmap];0.83[JPT][hapmap]
rs10478283	0.92[CEU][hapmap];0.89[CHB][hapmap];0.82[JPT][hapmap]
rs10900713	0.92[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap]
rs12055304	0.92[CEU][hapmap];0.89[CHB][hapmap];0.82[JPT][hapmap]
rs1421842	0.80[ASN][1000 genomes]
rs153590	0.83[JPT][hapmap];0.81[ASN][1000 genomes]
rs153613	0.80[ASN][1000 genomes]
rs168826	0.81[ASN][1000 genomes]
rs2416431	0.92[CEU][hapmap];0.84[CHB][hapmap];0.82[JPT][hapmap]
rs4920906	0.92[CEU][hapmap];0.89[CHB][hapmap];0.82[JPT][hapmap]
rs4921066	1.00[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap]
rs6594950	0.92[CEU][hapmap];0.89[CHB][hapmap];0.82[JPT][hapmap]
rs6594954	0.92[CEU][hapmap];0.89[CHB][hapmap];0.82[JPT][hapmap]
rs6594955	0.93[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap]
rs6877029	1.00[CEU][hapmap];0.89[CHB][hapmap];0.82[JPT][hapmap]
rs6878279	0.93[CEU][hapmap];0.85[CHB][hapmap];0.83[JPT][hapmap]
rs712572	0.80[ASN][1000 genomes]
rs712573	0.81[ASN][1000 genomes]
rs712576	0.86[AMR][1000 genomes]
rs712577	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs712578	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs712583	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs712584	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs712585	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs712587	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs712589	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7704903	0.92[CEU][hapmap];0.89[CHB][hapmap]
rs785371	0.80[AMR][1000 genomes]
rs785372	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs785376	0.95[ASN][1000 genomes]
rs9326993	0.93[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34146	chr5:115315944-115729919	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	esv2755349	chr5:115384101-115733101	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv882746	chr5:115566026-115704566	Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv882747	chr5:115566636-115662510	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1017983	chr5:115578765-115713688	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv882748	chr5:115584159-115669950	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv869754	chr5:115634234-115696094	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv4968	chr5:115635771-115714856	Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1018001	chr5:115640603-115660285	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115634200-115664400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr5:115640800-115658200	Weak transcription	Colonic Mucosa	Colon
3	chr5:115642000-115654200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr5:115642600-115654400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr5:115642800-115655800	Weak transcription	Fetal Thymus	thymus
6	chr5:115643000-115656800	Weak transcription	Gastric	stomach
7	chr5:115643200-115660200	Weak transcription	Placenta	Placenta
8	chr5:115643200-115664200	Weak transcription	Thymus	Thymus
9	chr5:115643200-115664800	Weak transcription	Pancreas	Pancrea
10	chr5:115643200-115669800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr5:115644000-115658600	Weak transcription	HSMM	muscle
12	chr5:115644200-115655800	Weak transcription	HUVEC	blood vessel
13	chr5:115644400-115654200	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr5:115644400-115664800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr5:115644400-115671800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr5:115646400-115656000	Weak transcription	Fetal Kidney	kidney
17	chr5:115647600-115660400	Weak transcription	Small Intestine	intestine
18	chr5:115648400-115655200	Weak transcription	Fetal Stomach	stomach
19	chr5:115649000-115692800	Weak transcription	Fetal Heart	heart
20	chr5:115649200-115654000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr5:115649200-115663200	Weak transcription	HSMMtube	muscle
22	chr5:115649400-115654000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:115649600-115656600	Weak transcription	Colon Smooth Muscle	Colon
24	chr5:115649600-115658000	Strong transcription	Primary T helper cells PMA-I stimulated	--
25	chr5:115649800-115656000	Weak transcription	Liver	Liver
26	chr5:115650200-115655400	Strong transcription	Adipose Nuclei	Adipose
27	chr5:115650800-115659200	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr5:115651400-115654600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr5:115651800-115655400	Strong transcription	Left Ventricle	heart
30	chr5:115652000-115656000	Weak transcription	Osteobl	bone
31	chr5:115652000-115665000	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr5:115652000-115668000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr5:115652200-115654400	ZNF genes & repeats	Primary B cells from peripheral blood	blood
34	chr5:115652200-115655800	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr5:115652600-115654800	Strong transcription	Duodenum Mucosa	Duodenum
36	chr5:115652600-115655200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
37	chr5:115652600-115655400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
38	chr5:115652800-115654200	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
39	chr5:115652800-115654400	ZNF genes & repeats	Primary T cells from cord blood	blood
40	chr5:115652800-115655400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr5:115652800-115655400	Strong transcription	Pancreatic Islets	Pancreatic Islet
42	chr5:115652800-115655800	Weak transcription	HepG2	liver
43	chr5:115652800-115656400	Strong transcription	Primary T helper naive cells from peripheral blood	blood
44	chr5:115652800-115659400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr5:115653000-115654000	ZNF genes & repeats	Fetal Intestine Large	intestine
46	chr5:115653000-115654400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
47	chr5:115653000-115654400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
48	chr5:115653000-115654400	ZNF genes & repeats	Brain Substantia Nigra	brain
49	chr5:115653000-115654400	ZNF genes & repeats	Ovary	ovary
50	chr5:115653000-115654400	Strong transcription	Skeletal Muscle Male	skeletal muscle

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