Variant report

Variant	rs712574
Chromosome Location	chr5:115645582-115645583
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10063312	0.80[CHD][hapmap]
rs10066081	0.82[CHB][hapmap]
rs10078121	0.86[CHB][hapmap];0.90[CHD][hapmap];0.83[GIH][hapmap];0.80[JPT][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap]
rs10079176	0.82[CHB][hapmap]
rs10079691	0.82[CHD][hapmap]
rs1090078	0.83[ASN][1000 genomes]
rs12109104	0.82[CHB][hapmap];0.80[CHD][hapmap];0.81[ASN][1000 genomes]
rs12657249	0.82[CHD][hapmap]
rs1382343	0.81[ASN][1000 genomes]
rs1382344	0.81[ASN][1000 genomes]
rs149131	0.84[ASN][1000 genomes]
rs1508875	0.82[CHD][hapmap]
rs153593	0.84[ASN][1000 genomes]
rs153594	0.84[ASN][1000 genomes]
rs1644268	0.83[ASN][1000 genomes]
rs1677406	0.82[CHB][hapmap];0.81[ASN][1000 genomes]
rs173834	0.91[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs185263	0.83[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs253950	0.80[CHD][hapmap];0.81[ASN][1000 genomes]
rs253951	0.83[ASN][1000 genomes]
rs253952	0.83[ASN][1000 genomes]
rs253959	0.82[CHB][hapmap];0.80[CHD][hapmap]
rs254150	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs254151	0.87[CHB][hapmap];0.90[CHD][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs254152	0.94[ASW][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs254171	0.82[CHB][hapmap];0.81[ASN][1000 genomes]
rs254172	0.82[CHB][hapmap];0.81[ASN][1000 genomes]
rs254173	0.82[CHB][hapmap];0.81[ASN][1000 genomes]
rs254174	0.82[CHB][hapmap];0.82[CHD][hapmap];0.81[ASN][1000 genomes]
rs27125	0.84[ASN][1000 genomes]
rs27126	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs37180	0.81[ASN][1000 genomes]
rs40192	0.81[ASN][1000 genomes]
rs41271	0.81[ASN][1000 genomes]
rs712576	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs712577	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs712591	0.88[ASN][1000 genomes]
rs712601	0.86[ASN][1000 genomes]
rs7735539	0.82[CHD][hapmap]
rs784479	0.82[CHB][hapmap];0.81[ASN][1000 genomes]
rs784481	0.81[ASN][1000 genomes]
rs785367	0.94[ASW][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.82[MEX][hapmap];0.97[MKK][hapmap];0.89[TSI][hapmap];0.89[YRI][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs785369	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs785370	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs785371	0.88[ASN][1000 genomes]
rs785373	0.88[ASN][1000 genomes]
rs785375	0.87[ASN][1000 genomes]
rs785377	0.86[ASN][1000 genomes]
rs803967	0.82[CHB][hapmap]
rs809210	0.81[ASN][1000 genomes]
rs810742	0.81[ASN][1000 genomes]

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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs712574	COMMD10	cis	lymphoblastoid	seeQTL

Chromatin state (count:51 , 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	chr5:115634400-115645600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:115639600-115647400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr5:115640200-115645600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
5	chr5:115640200-115647200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
6	chr5:115640400-115645800	ZNF genes & repeats	Primary T cells from cord blood	blood
7	chr5:115640600-115645600	ZNF genes & repeats	Adipose Nuclei	Adipose
8	chr5:115640800-115645600	ZNF genes & repeats	Primary B cells from cord blood	blood
9	chr5:115640800-115658200	Weak transcription	Colonic Mucosa	Colon
10	chr5:115641000-115653000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:115641400-115645600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
12	chr5:115641400-115651800	Weak transcription	Esophagus	oesophagus
13	chr5:115641600-115647200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr5:115642000-115654200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr5:115642400-115645600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
16	chr5:115642400-115653000	Weak transcription	Rectal Smooth Muscle	rectum
17	chr5:115642600-115646000	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
18	chr5:115642600-115654400	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr5:115642800-115650800	Weak transcription	A549	lung
20	chr5:115642800-115655800	Weak transcription	Fetal Thymus	thymus
21	chr5:115643000-115648200	Weak transcription	Fetal Stomach	stomach
22	chr5:115643000-115653000	Weak transcription	Right Ventricle	heart
23	chr5:115643000-115656800	Weak transcription	Gastric	stomach
24	chr5:115643200-115650200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr5:115643200-115660200	Weak transcription	Placenta	Placenta
26	chr5:115643200-115664200	Weak transcription	Thymus	Thymus
27	chr5:115643200-115664800	Weak transcription	Pancreas	Pancrea
28	chr5:115643200-115669800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr5:115643400-115646800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr5:115643600-115645600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
31	chr5:115644000-115649000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr5:115644000-115649000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr5:115644000-115658600	Weak transcription	HSMM	muscle
34	chr5:115644200-115653200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr5:115644200-115655800	Weak transcription	HUVEC	blood vessel
36	chr5:115644400-115653000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr5:115644400-115653200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr5:115644400-115654200	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr5:115644400-115664800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr5:115644400-115671800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr5:115644800-115645600	ZNF genes & repeats	Psoas Muscle	Psoas
42	chr5:115645000-115651200	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr5:115645000-115653000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr5:115645200-115645600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr5:115645200-115653000	Weak transcription	Lung	lung
46	chr5:115645200-115653000	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr5:115645400-115645600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr5:115645400-115645600	Strong transcription	Left Ventricle	heart
49	chr5:115645400-115649800	Weak transcription	Aorta	Aorta
50	chr5:115645400-115650000	Weak transcription	Primary T helper cells fromperipheralblood	blood

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