Variant report

Variant	rs17225088
Chromosome Location	chr2:47711988-47711989
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:47710471..47713056-chr2:47714983..47716498,2	K562	blood:
2	chr2:47710962..47713077-chr2:47751330..47753151,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000236558	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs17036630	1.00[EUR][1000 genomes]
rs17218160	1.00[EUR][1000 genomes]
rs17218452	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72872831	1.00[EUR][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	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

No data

Chromatin state (count:119 , 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	chr2:47658000-47714200	Weak transcription	Small Intestine	intestine
4	chr2:47658200-47713400	Weak transcription	Fetal Heart	heart
5	chr2:47658200-47714200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr2:47658200-47714800	Weak transcription	HSMMtube	muscle
7	chr2:47658200-47724800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr2:47658400-47713600	Weak transcription	Stomach Smooth Muscle	stomach
9	chr2:47658400-47716000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr2:47658800-47712600	Weak transcription	Osteobl	bone
11	chr2:47673800-47712400	Weak transcription	NHDF-Ad	bronchial
12	chr2:47679800-47712600	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr2:47685000-47715000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:47686400-47712600	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr2:47686400-47712600	Strong transcription	Dnd41	blood
16	chr2:47689200-47713000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:47689400-47712800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr2:47689800-47713000	Strong transcription	H1 Cell Line	embryonic stem cell
19	chr2:47691000-47714000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr2:47691600-47714200	Weak transcription	Ovary	ovary
21	chr2:47691600-47714400	Weak transcription	Spleen	Spleen
22	chr2:47691600-47715400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr2:47691600-47715600	Weak transcription	NHEK	skin
24	chr2:47691600-47716000	Weak transcription	Gastric	stomach
25	chr2:47691600-47716000	Weak transcription	Pancreas	Pancrea
26	chr2:47692000-47714400	Weak transcription	Placenta	Placenta
27	chr2:47692200-47712800	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr2:47692800-47712800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr2:47692800-47713400	Strong transcription	HUES48 Cell Line	embryonic stem cell
30	chr2:47693200-47713600	Weak transcription	Rectal Smooth Muscle	rectum
31	chr2:47693600-47715400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:47693600-47716800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr2:47694200-47715600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr2:47696000-47716000	Weak transcription	NHLF	lung
35	chr2:47696800-47716000	Weak transcription	Lung	lung
36	chr2:47697000-47714400	Weak transcription	Esophagus	oesophagus
37	chr2:47697000-47716200	Weak transcription	Fetal Brain Female	brain
38	chr2:47697200-47715400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr2:47697600-47715600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr2:47697800-47712400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr2:47699000-47714200	Weak transcription	Brain Anterior Caudate	brain
42	chr2:47699200-47713400	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr2:47699200-47714200	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr2:47700400-47714800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr2:47700600-47714400	Weak transcription	Brain Germinal Matrix	brain
46	chr2:47702200-47712600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr2:47702400-47712000	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr2:47702400-47714200	Weak transcription	Aorta	Aorta
49	chr2:47702800-47727000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr2:47703000-47713200	Weak transcription	Sigmoid Colon	Sigmoid Colon

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