Variant report

Variant	rs11653539
Chromosome Location	chr17:46581561-46581562
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:46581475..46583827-chr17:46593469..46596750,3	MCF-7	breast:
2	chr17:46579782..46582446-chr17:46602782..46604521,2	MCF-7	breast:
3	chr17:46580131..46581682-chr20:55568889..55570521,2	MCF-7	breast:
4	chr17:46575874..46579148-chr17:46581240..46583659,4	MCF-7	breast:
5	chr17:46574112..46575706-chr17:46580959..46582706,2	MCF-7	breast:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11650389	1.00[EUR][1000 genomes]
rs11651053	0.87[EUR][1000 genomes]
rs11652654	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11653644	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11655171	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11655546	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11657206	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2740759	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs59709353	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7209524	1.00[CEU][hapmap]
rs73985866	0.87[EUR][1000 genomes]
rs7406478	1.00[CEU][hapmap]
rs8065730	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9747570	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833469	chr17:46491849-46709406	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
2	esv3420538	chr17:46504944-46861553	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	369 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:46574600-46588000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr17:46574800-46582800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr17:46574800-46582800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr17:46574800-46582800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr17:46576800-46582000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr17:46577200-46582000	Enhancers	Fetal Stomach	stomach
7	chr17:46578400-46582800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr17:46578600-46582600	Weak transcription	HSMM	muscle
9	chr17:46578600-46583000	Weak transcription	HSMMtube	muscle
10	chr17:46578800-46582600	Weak transcription	NH-A	brain
11	chr17:46578800-46583000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr17:46578800-46583200	Weak transcription	NHLF	lung
13	chr17:46579000-46581600	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr17:46579200-46581600	Weak transcription	A549	lung
15	chr17:46580200-46582200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr17:46580200-46584600	Enhancers	Placenta Amnion	Placenta Amnion
17	chr17:46580400-46582000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr17:46580600-46581800	Bivalent Enhancer	Fetal Heart	heart
19	chr17:46580800-46582000	Enhancers	Rectal Smooth Muscle	rectum
20	chr17:46580800-46582400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr17:46580800-46584000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr17:46581000-46581600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr17:46581000-46581600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr17:46581000-46581800	Bivalent Enhancer	Fetal Intestine Large	intestine
25	chr17:46581000-46581800	Enhancers	Placenta	Placenta
26	chr17:46581000-46581800	Enhancers	K562	blood
27	chr17:46581000-46582000	Enhancers	Colon Smooth Muscle	Colon
28	chr17:46581200-46581600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
29	chr17:46581200-46581800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr17:46581200-46582200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
31	chr17:46581200-46582200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
32	chr17:46581400-46581600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
33	chr17:46581400-46581600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr17:46581400-46582200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
35	chr17:46581400-46582400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr17:46581400-46582600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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