Variant report

Variant	rs814681
Chromosome Location	chr9:116720761-116720762
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:116715151..116717735-chr9:116720132..116722087,2	MCF-7	breast:
2	chr9:116718450..116721380-chr9:116821221..116823441,2	MCF-7	breast:
3	chr9:116720397..116723417-chr9:116724656..116727366,3	MCF-7	breast:
4	chr9:116714888..116717726-chr9:116720128..116722306,2	K562	blood:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs16910855	1.00[AMR][1000 genomes]
rs16910950	1.00[AMR][1000 genomes]
rs16910968	0.91[EUR][1000 genomes]
rs2761689	0.91[EUR][1000 genomes]
rs2761690	0.91[EUR][1000 genomes]
rs35678978	1.00[AMR][1000 genomes]
rs4287014	1.00[AMR][1000 genomes]
rs7041279	0.91[EUR][1000 genomes]
rs73554413	1.00[AMR][1000 genomes]
rs73554494	1.00[AMR][1000 genomes]
rs814678	1.00[EUR][1000 genomes]
rs814679	0.91[EUR][1000 genomes]
rs814682	0.91[EUR][1000 genomes]
rs814683	0.91[EUR][1000 genomes]
rs814684	0.91[EUR][1000 genomes]
rs814685	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs814687	0.91[EUR][1000 genomes]
rs814688	0.91[EUR][1000 genomes]
rs814689	0.87[EUR][1000 genomes]
rs814690	0.91[EUR][1000 genomes]
rs814691	0.91[EUR][1000 genomes]
rs814692	0.91[EUR][1000 genomes]
rs814693	0.91[EUR][1000 genomes]
rs814694	0.91[EUR][1000 genomes]
rs814695	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430093	chr9:116330446-117325446	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116708800-116726400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr9:116710800-116723000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:116712800-116726400	Weak transcription	Brain Germinal Matrix	brain
4	chr9:116714400-116721200	Enhancers	NHDF-Ad	bronchial
5	chr9:116714600-116721600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr9:116714600-116722400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr9:116715000-116721000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr9:116715000-116721200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr9:116716000-116720800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr9:116716200-116730000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr9:116716800-116721000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:116716800-116723000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:116717000-116720800	Enhancers	Adipose Nuclei	Adipose
14	chr9:116717000-116720800	Enhancers	Fetal Lung	lung
15	chr9:116717000-116721200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr9:116717000-116723400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr9:116717000-116730000	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr9:116717000-116733200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr9:116717200-116754600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr9:116717400-116735600	Weak transcription	Fetal Heart	heart
21	chr9:116717600-116730200	Weak transcription	Psoas Muscle	Psoas
22	chr9:116717800-116720800	Enhancers	HSMMtube	muscle
23	chr9:116717800-116724800	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr9:116718000-116731400	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr9:116718400-116728600	Weak transcription	Primary hematopoietic stem cells	blood
26	chr9:116718600-116721000	Enhancers	Ovary	ovary
27	chr9:116718600-116731000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr9:116718800-116720800	Enhancers	Aorta	Aorta
29	chr9:116719200-116721000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr9:116719200-116721200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr9:116719200-116721200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr9:116719400-116721000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr9:116719400-116721000	Enhancers	Fetal Stomach	stomach
34	chr9:116719400-116721000	Enhancers	Stomach Mucosa	stomach
35	chr9:116719400-116721000	Enhancers	HMEC	breast
36	chr9:116719400-116721200	Enhancers	Lung	lung
37	chr9:116719400-116721200	Enhancers	Pancreas	Pancrea
38	chr9:116719600-116720800	Enhancers	H1 Cell Line	embryonic stem cell
39	chr9:116719600-116720800	Enhancers	Fetal Muscle Leg	muscle
40	chr9:116719600-116720800	Flanking Active TSS	A549	lung
41	chr9:116719600-116721000	Enhancers	Liver	Liver
42	chr9:116719600-116721000	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr9:116719600-116721200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr9:116719800-116720800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr9:116719800-116720800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr9:116719800-116720800	Enhancers	Fetal Muscle Trunk	muscle
47	chr9:116719800-116720800	Enhancers	Placenta Amnion	Placenta Amnion
48	chr9:116719800-116721000	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr9:116719800-116721000	Enhancers	Fetal Intestine Small	intestine
50	chr9:116719800-116721000	Enhancers	Rectal Mucosa Donor 31	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links