Variant report

Variant	rs72886367
Chromosome Location	chr2:47704443-47704444
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:47704258..47706213-chr2:47706968..47708796,2	K562	blood:
2	chr2:47703532..47706213-chr2:47706572..47708796,3	K562	blood:

Variant related genes	Relation type
ENSG00000095002	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11901715	1.00[AMR][1000 genomes]
rs57831950	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57916992	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57945178	1.00[AMR][1000 genomes]
rs58882508	1.00[AMR][1000 genomes]
rs58931241	1.00[AMR][1000 genomes]
rs59248614	1.00[AMR][1000 genomes]
rs59927838	1.00[AMR][1000 genomes]
rs60068970	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60358586	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60518577	1.00[AMR][1000 genomes]
rs60887102	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60998282	1.00[AMR][1000 genomes]
rs61212083	1.00[AMR][1000 genomes]
rs61451736	1.00[AMR][1000 genomes]
rs72872806	1.00[AMR][1000 genomes]
rs72872810	1.00[AMR][1000 genomes]
rs72882704	1.00[AMR][1000 genomes]
rs72882709	1.00[AMR][1000 genomes]
rs72882712	1.00[AMR][1000 genomes]
rs72882715	1.00[AMR][1000 genomes]
rs72882770	1.00[AMR][1000 genomes]
rs72884694	1.00[AMR][1000 genomes]
rs72884701	1.00[AMR][1000 genomes]
rs72886311	1.00[AMR][1000 genomes]
rs72886331	1.00[AMR][1000 genomes]
rs72886333	1.00[AMR][1000 genomes]
rs72886340	1.00[AMR][1000 genomes]
rs72886346	1.00[AMR][1000 genomes]
rs72886357	1.00[AMR][1000 genomes]
rs72888235	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72888241	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72888249	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72888257	1.00[AMR][1000 genomes]
rs72888260	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72888262	1.00[AMR][1000 genomes]
rs72888268	1.00[AMR][1000 genomes]
rs72888274	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72888288	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72890160	1.00[AMR][1000 genomes]
rs72890162	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817517	chr2:46819371-47715140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv1004828	chr2:47056849-47814482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
3	nsv531348	chr2:47433147-47827310	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv999576	chr2:47506116-47773960	Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv527823	chr2:47645249-47709704	Genic enhancers Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47631400-47714400	Weak transcription	Right Ventricle	heart
2	chr2:47633000-47714000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr2:47658000-47707000	Weak transcription	Colon Smooth Muscle	Colon
4	chr2:47658000-47714200	Weak transcription	Small Intestine	intestine
5	chr2:47658200-47709200	Weak transcription	Brain Substantia Nigra	brain
6	chr2:47658200-47710400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr2:47658200-47713400	Weak transcription	Fetal Heart	heart
8	chr2:47658200-47714200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr2:47658200-47714800	Weak transcription	HSMMtube	muscle
10	chr2:47658200-47724800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr2:47658400-47713600	Weak transcription	Stomach Smooth Muscle	stomach
12	chr2:47658400-47716000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr2:47658800-47712600	Weak transcription	Osteobl	bone
14	chr2:47673800-47712400	Weak transcription	NHDF-Ad	bronchial
15	chr2:47677000-47710800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr2:47679800-47712600	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr2:47685000-47715000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:47686400-47712600	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr2:47686400-47712600	Strong transcription	Dnd41	blood
20	chr2:47687200-47706800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
21	chr2:47689200-47713000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:47689400-47712800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr2:47689800-47713000	Strong transcription	H1 Cell Line	embryonic stem cell
24	chr2:47690000-47706800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr2:47690200-47706600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr2:47690200-47708200	Strong transcription	Fetal Thymus	thymus
27	chr2:47690200-47711000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr2:47691000-47714000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr2:47691600-47711600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:47691600-47714200	Weak transcription	Ovary	ovary
31	chr2:47691600-47714400	Weak transcription	Spleen	Spleen
32	chr2:47691600-47715400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:47691600-47715600	Weak transcription	NHEK	skin
34	chr2:47691600-47716000	Weak transcription	Gastric	stomach
35	chr2:47691600-47716000	Weak transcription	Pancreas	Pancrea
36	chr2:47692000-47714400	Weak transcription	Placenta	Placenta
37	chr2:47692200-47712800	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr2:47692800-47706200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
39	chr2:47692800-47712800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr2:47692800-47713400	Strong transcription	HUES48 Cell Line	embryonic stem cell
41	chr2:47693000-47711000	Weak transcription	Brain Angular Gyrus	brain
42	chr2:47693200-47713600	Weak transcription	Rectal Smooth Muscle	rectum
43	chr2:47693600-47715400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:47693600-47716800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr2:47694200-47715600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr2:47695800-47711400	Weak transcription	Fetal Brain Male	brain
47	chr2:47696000-47707800	Weak transcription	HSMM	muscle
48	chr2:47696000-47716000	Weak transcription	NHLF	lung
49	chr2:47696800-47716000	Weak transcription	Lung	lung
50	chr2:47697000-47714400	Weak transcription	Esophagus	oesophagus

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