Variant report

Variant	rs73285610
Chromosome Location	chr12:42705780-42705781
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs11385212	0.83[AMR][1000 genomes]
rs1234113	0.83[AMR][1000 genomes]
rs1683193	0.83[AMR][1000 genomes]
rs2639128	0.83[AMR][1000 genomes]
rs56669009	0.83[AMR][1000 genomes]
rs57166587	1.00[AMR][1000 genomes]
rs57260154	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57549495	0.83[AMR][1000 genomes]
rs57582332	0.83[AMR][1000 genomes]
rs58488818	1.00[AMR][1000 genomes]
rs58902406	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59321446	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60327465	0.83[AMR][1000 genomes]
rs60341977	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs712113	0.83[AMR][1000 genomes]
rs712117	0.83[AMR][1000 genomes]
rs712121	0.83[AMR][1000 genomes]
rs712128	0.83[AMR][1000 genomes]
rs7132315	0.83[AMR][1000 genomes]
rs7136339	1.00[AMR][1000 genomes]
rs7298660	0.83[AMR][1000 genomes]
rs7303532	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73270272	0.83[AMR][1000 genomes]
rs73272006	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73272039	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73272041	1.00[AMR][1000 genomes]
rs73272052	1.00[AMR][1000 genomes]
rs73272054	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73272065	1.00[AMR][1000 genomes]
rs73273905	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73273908	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73273915	1.00[AMR][1000 genomes]
rs73273940	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73273948	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73280071	0.83[AMR][1000 genomes]
rs73280079	0.83[AMR][1000 genomes]
rs73280085	0.83[AMR][1000 genomes]
rs73280087	0.83[AMR][1000 genomes]
rs73280101	0.83[AMR][1000 genomes]
rs73281848	0.83[AMR][1000 genomes]
rs73281857	0.83[AMR][1000 genomes]
rs73281868	0.83[AMR][1000 genomes]
rs73281890	0.83[AMR][1000 genomes]
rs73281897	0.83[AMR][1000 genomes]
rs73283726	0.83[AMR][1000 genomes]
rs73283728	0.83[AMR][1000 genomes]
rs73283731	0.83[AMR][1000 genomes]
rs73283737	0.83[AMR][1000 genomes]
rs73283752	0.83[AMR][1000 genomes]
rs73283757	0.83[AMR][1000 genomes]
rs73283764	0.83[AMR][1000 genomes]
rs73283782	1.00[AMR][1000 genomes]
rs73285606	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73285607	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73285625	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73285647	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73285664	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73285666	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73285678	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078990	1.00[AMR][1000 genomes]
rs7957401	0.83[AMR][1000 genomes]
rs7960285	0.83[AMR][1000 genomes]
rs7964994	0.83[AMR][1000 genomes]
rs850828	0.83[AMR][1000 genomes]
rs864291	0.83[AMR][1000 genomes]
rs864298	0.83[AMR][1000 genomes]
rs9669751	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430505	chr12:42297931-42720773	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv1048971	chr12:42651976-42801204	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1044790	chr12:42672255-43344184	Enhancers Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
4	nsv541483	chr12:42672255-43344184	Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:42690800-42706400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:42693600-42706200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr12:42693600-42719000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr12:42693800-42708400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr12:42694000-42706800	Weak transcription	A549	lung
6	chr12:42694000-42707000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr12:42695200-42710600	Weak transcription	GM12878-XiMat	blood
8	chr12:42695600-42714800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr12:42696200-42709000	Weak transcription	K562	blood
10	chr12:42696200-42718800	Weak transcription	Brain Hippocampus Middle	brain
11	chr12:42696800-42707000	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr12:42697000-42718800	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr12:42697200-42710600	Weak transcription	Ovary	ovary
14	chr12:42697400-42718000	Weak transcription	HepG2	liver
15	chr12:42698800-42706800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr12:42699400-42706800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:42699600-42718800	Weak transcription	HUVEC	blood vessel
18	chr12:42699800-42718200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr12:42700800-42716400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr12:42701000-42706800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr12:42701200-42718600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr12:42701400-42717400	Weak transcription	Pancreas	Pancrea
23	chr12:42701600-42706800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr12:42701800-42706200	Weak transcription	Adipose Nuclei	Adipose
25	chr12:42701800-42706800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr12:42701800-42707000	Weak transcription	Fetal Brain Female	brain
27	chr12:42701800-42712200	Weak transcription	Thymus	Thymus
28	chr12:42701800-42718600	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr12:42701800-42718800	Weak transcription	Brain Angular Gyrus	brain
30	chr12:42701800-42719400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:42702000-42706800	Weak transcription	Fetal Thymus	thymus
32	chr12:42702000-42707400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr12:42702200-42706800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr12:42702200-42718600	Weak transcription	Brain Substantia Nigra	brain
35	chr12:42702400-42707000	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr12:42702400-42714600	Weak transcription	Brain Germinal Matrix	brain
37	chr12:42702600-42706600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr12:42702600-42706800	Weak transcription	Placenta	Placenta
39	chr12:42702600-42707000	Weak transcription	Primary T cells from cord blood	blood
40	chr12:42702600-42707200	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr12:42702600-42718800	Weak transcription	Colon Smooth Muscle	Colon
42	chr12:42702800-42706800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr12:42702800-42706800	Weak transcription	Primary B cells from cord blood	blood
44	chr12:42702800-42712200	Weak transcription	Stomach Smooth Muscle	stomach
45	chr12:42703000-42706000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr12:42703000-42707000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr12:42703000-42717400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr12:42703400-42707400	Weak transcription	Primary hematopoietic stem cells	blood
49	chr12:42703400-42708000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr12:42703600-42706800	Weak transcription	Fetal Intestine Large	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links