Variant report

Variant	rs60100807
Chromosome Location	chr2:46691781-46691782
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:46691531..46694095-chr2:46695293..46698690,3	K562	blood:
2	chr2:46691709..46692306-chr2:46768561..46769542,2	MCF-7	breast:
3	chr2:46688831..46694095-chr2:46695879..46699021,6	K562	blood:
4	chr2:46691026..46692360-chr2:46877376..46878456,8	K562	blood:
5	chr2:46691367..46692063-chr2:46877281..46878815,4	MCF-7	breast:
6	chr2:46691364..46692337-chr2:46828238..46828952,3	K562	blood:
7	chr2:46691590..46692280-chr2:46828551..46829170,2	MCF-7	breast:
8	chr2:46691358..46692227-chr2:47115825..47116785,3	K562	blood:
9	chr2:46691374..46692262-chr2:46827993..46829151,4	MCF-7	breast:
10	chr2:46689308..46691938-chr2:46875674..46878193,3	MCF-7	breast:
11	chr2:46691759..46692350-chr2:47003556..47004124,2	K562	blood:
12	chr2:46690352..46691867-chr2:46842871..46845285,2	K562	blood:
13	chr2:46691412..46692513-chr2:47115934..47116752,3	MCF-7	breast:
14	chr2:46691583..46692300-chr2:46844576..46845112,2	MCF-7	breast:
15	chr2:46690029..46692779-chr2:46842870..46844853,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000119878	Chromatin interaction
ENSG00000119729	Chromatin interaction
ENSG00000250565	Chromatin interaction
ENSG00000151665	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs55680262	1.00[AFR][1000 genomes]
rs55768552	0.83[AFR][1000 genomes]
rs55770522	1.00[AFR][1000 genomes]
rs55775849	0.83[AFR][1000 genomes]
rs55846419	0.83[AFR][1000 genomes]
rs55857444	1.00[AFR][1000 genomes]
rs55858852	0.83[AFR][1000 genomes]
rs55909007	0.83[AFR][1000 genomes]
rs55936500	0.83[AFR][1000 genomes]
rs55939277	0.83[AFR][1000 genomes]
rs56194963	1.00[AFR][1000 genomes]
rs56352638	0.83[AFR][1000 genomes]
rs57134112	0.83[AFR][1000 genomes]
rs57134197	1.00[AFR][1000 genomes]
rs57326818	0.83[AFR][1000 genomes]
rs57453502	1.00[AFR][1000 genomes]
rs57596928	0.83[AFR][1000 genomes]
rs57823622	0.83[AFR][1000 genomes]
rs58143719	1.00[AFR][1000 genomes]
rs58202206	0.83[AFR][1000 genomes]
rs58267234	0.83[AFR][1000 genomes]
rs58395052	1.00[AFR][1000 genomes]
rs58639867	0.83[AFR][1000 genomes]
rs60086470	1.00[AFR][1000 genomes]
rs60337602	0.83[AFR][1000 genomes]
rs60358116	0.83[AFR][1000 genomes]
rs61599272	0.83[AFR][1000 genomes]
rs6756900	0.83[AFR][1000 genomes]
rs73926284	0.83[AFR][1000 genomes]
rs73926287	0.83[AFR][1000 genomes]
rs73926290	0.83[AFR][1000 genomes]
rs73926291	0.83[AFR][1000 genomes]
rs73926293	0.83[AFR][1000 genomes]
rs73927846	0.83[AFR][1000 genomes]
rs73927849	0.83[AFR][1000 genomes]
rs73927872	0.83[AFR][1000 genomes]
rs73929724	0.83[AFR][1000 genomes]
rs73929725	0.83[AFR][1000 genomes]
rs73929728	0.83[AFR][1000 genomes]
rs73929729	0.83[AFR][1000 genomes]
rs73929730	0.83[AFR][1000 genomes]
rs73929731	1.00[AFR][1000 genomes]
rs73929737	0.83[AFR][1000 genomes]
rs873532	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012446	chr2:45921682-46737036	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	esv2757795	chr2:46532812-46874151	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	esv2759046	chr2:46532812-46874151	Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	esv34650	chr2:46605659-46818992	Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	esv2756919	chr2:46614235-46756431	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
6	nsv437435	chr2:46636967-46763587	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	esv34937	chr2:46651624-46818586	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
8	nsv581745	chr2:46660445-46693963	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
9	nsv9702	chr2:46668106-46745740	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
10	nsv817828	chr2:46670146-46739157	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv1014425	chr2:46670179-47033417	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
12	nsv535678	chr2:46670179-47033417	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
13	nsv873996	chr2:46670941-47065227	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
14	nsv519216	chr2:46683683-46723219	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:46686400-46704400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:46687600-46691800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr2:46687800-46691800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:46688400-46691800	Enhancers	Osteobl	bone
5	chr2:46688600-46691800	Weak transcription	Brain Germinal Matrix	brain
6	chr2:46688800-46691800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr2:46689000-46696800	Weak transcription	K562	blood
8	chr2:46689200-46691800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr2:46689200-46696600	Weak transcription	Fetal Thymus	thymus
10	chr2:46689200-46698600	Weak transcription	Hela-S3	cervix
11	chr2:46689200-46704800	Weak transcription	Placenta	Placenta
12	chr2:46689200-46714800	Weak transcription	Right Atrium	heart
13	chr2:46689600-46691800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr2:46689800-46697000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr2:46689800-46697400	Weak transcription	Primary B cells from peripheral blood	blood
16	chr2:46690000-46691800	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr2:46690000-46696800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr2:46691000-46691800	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr2:46691200-46691800	Enhancers	Adipose Nuclei	Adipose
20	chr2:46691200-46691800	Enhancers	Colon Smooth Muscle	Colon
21	chr2:46691200-46691800	Enhancers	Left Ventricle	heart
22	chr2:46691200-46691800	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr2:46691200-46692000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr2:46691200-46692000	Enhancers	Brain Substantia Nigra	brain
25	chr2:46691400-46691800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr2:46691400-46691800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr2:46691400-46691800	Enhancers	Fetal Heart	heart
28	chr2:46691400-46691800	Enhancers	Right Ventricle	heart
29	chr2:46691400-46691800	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr2:46691400-46692000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr2:46691400-46692000	Enhancers	Brain Angular Gyrus	brain
32	chr2:46691400-46692000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr2:46691400-46692000	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr2:46691400-46692000	Enhancers	Stomach Smooth Muscle	stomach
35	chr2:46691400-46692000	Enhancers	A549	lung
36	chr2:46691400-46692400	Enhancers	Brain Cingulate Gyrus	brain
37	chr2:46691400-46692400	Enhancers	Brain Hippocampus Middle	brain
38	chr2:46691400-46692600	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr2:46691400-46692800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr2:46691400-46693000	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr2:46691600-46691800	Enhancers	Brain Anterior Caudate	brain
42	chr2:46691600-46691800	Enhancers	Fetal Brain Female	brain
43	chr2:46691600-46692000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr2:46691600-46692600	Enhancers	Fetal Brain Male	brain
45	chr2:46691600-46696800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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