Variant report

Variant	rs1875059
Chromosome Location	chr12:32702900-32702901
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11052068	1.00[CHB][hapmap]
rs34072072	0.95[ASN][1000 genomes]
rs34759311	0.97[ASN][1000 genomes]
rs35944077	0.95[ASN][1000 genomes]
rs4931635	1.00[CHB][hapmap];0.84[CHD][hapmap];0.88[JPT][hapmap]
rs4931636	1.00[CHB][hapmap];0.84[CHD][hapmap]
rs6488063	1.00[CHB][hapmap];0.84[CHD][hapmap];0.88[JPT][hapmap]
rs7135097	1.00[ASW][hapmap]
rs7964106	1.00[CHB][hapmap];0.84[CHD][hapmap];0.88[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531960	chr12:32257285-32775277	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1054191	chr12:32534619-32733066	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv541455	chr12:32534619-32733066	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	esv3342938	chr12:32551041-32716745	Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1037224	chr12:32698189-32721994	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv541456	chr12:32698189-32721994	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32693000-32729600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:32696000-32704200	Enhancers	Ovary	ovary
3	chr12:32697400-32704200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:32697800-32703200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr12:32698800-32719600	Weak transcription	Colonic Mucosa	Colon
6	chr12:32699200-32704200	Enhancers	Left Ventricle	heart
7	chr12:32699200-32705600	Enhancers	Psoas Muscle	Psoas
8	chr12:32699400-32704200	Enhancers	Lung	lung
9	chr12:32699600-32714800	Weak transcription	Fetal Intestine Large	intestine
10	chr12:32700000-32711400	Weak transcription	HepG2	liver
11	chr12:32700600-32703600	Enhancers	Fetal Muscle Leg	muscle
12	chr12:32701000-32703000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr12:32701000-32703000	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr12:32701000-32703000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr12:32701000-32703000	Enhancers	Fetal Lung	lung
16	chr12:32701000-32703000	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr12:32701000-32703200	Enhancers	Stomach Mucosa	stomach
18	chr12:32701200-32703000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr12:32701200-32703000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr12:32701200-32703000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
21	chr12:32701200-32703000	Enhancers	HMEC	breast
22	chr12:32701400-32703000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr12:32701400-32703000	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr12:32701400-32703000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr12:32701400-32703000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr12:32701400-32703000	Enhancers	Fetal Stomach	stomach
27	chr12:32701400-32703200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
28	chr12:32701400-32703200	Flanking Active TSS	Stomach Smooth Muscle	stomach
29	chr12:32701400-32703200	Flanking Active TSS	NHDF-Ad	bronchial
30	chr12:32701600-32703000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr12:32701600-32703000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr12:32701600-32703000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr12:32701600-32703000	Enhancers	Aorta	Aorta
34	chr12:32701600-32703000	Enhancers	Pancreas	Pancrea
35	chr12:32701600-32703000	Enhancers	Right Ventricle	heart
36	chr12:32701600-32703000	Enhancers	Spleen	Spleen
37	chr12:32701600-32703000	Flanking Active TSS	HSMMtube	muscle
38	chr12:32701600-32703400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr12:32701600-32704200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr12:32701600-32704200	Enhancers	Primary B cells from peripheral blood	blood
41	chr12:32701800-32703000	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr12:32701800-32703000	Flanking Active TSS	Brain Hippocampus Middle	brain
43	chr12:32701800-32703000	Flanking Active TSS	Fetal Heart	heart
44	chr12:32701800-32703200	Enhancers	Osteobl	bone
45	chr12:32701800-32711400	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr12:32702000-32703000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr12:32702000-32703000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr12:32702000-32703000	Flanking Active TSS	Brain Angular Gyrus	brain
49	chr12:32702000-32703000	Enhancers	Small Intestine	intestine
50	chr12:32702000-32703400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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