Variant report

Variant	nsv1028531
Chromosome Location	chr5:8138412-8193933
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr5:8176221-8176582	K562	blood:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
2	CEBPB	chr5:8150955-8151284	K562	blood:	n/a	chr5:8151114-8151125
3	CEBPB	chr5:8176051-8176638	Hela-S3	cervix:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
4	CEBPB	chr5:8138632-8138832	HepG2	liver:	n/a	chr5:8138707-8138718
5	CEBPB	chr5:8142028-8142376	HepG2	liver:	n/a	chr5:8142203-8142214
6	CEBPB	chr5:8176185-8176710	MCF-7	breast:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
7	CEBPB	chr5:8176268-8176497	HepG2	liver:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
8	CEBPB	chr5:8146783-8146820	K562	blood:	n/a	chr5:8146790-8146801 chr5:8146789-8146802
9	CEBPB	chr5:8142064-8142313	Hela-S3	cervix:	n/a	chr5:8142203-8142214
10	CEBPB	chr5:8176257-8176586	ECC-1	luminal epithelium:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
11	CEBPB	chr5:8176166-8176647	HepG2	liver:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
12	CEBPB	chr5:8176086-8176672	K562	blood:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
13	CEBPB	chr5:8150952-8151289	HepG2	liver:	n/a	chr5:8151114-8151125
14	CEBPB	chr5:8176076-8176792	A549	lung:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
15	CEBPB	chr5:8176228-8176611	HepG2	liver:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
16	CEBPB	chr5:8176120-8176702	MCF-7	breast:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
17	CEBPB	chr5:8176180-8176653	A549	lung:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
18	CEBPB	chr5:8176223-8176614	H1-hESC	embryonic stem cell:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
19	CEBPB	chr5:8150986-8151288	IMR90	lung:	n/a	chr5:8151114-8151125
20	CEBPB	chr5:8146709-8146905	HepG2	liver:	n/a	chr5:8146790-8146801 chr5:8146789-8146802
21	CEBPB	chr5:8142083-8142357	A549	lung:	n/a	chr5:8142203-8142214
22	CEBPB	chr5:8176222-8176613	HepG2	liver:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
23	CEBPB	chr5:8176289-8176531	K562	blood:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
24	CEBPB	chr5:8176175-8176615	IMR90	lung:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
25	CEBPB	chr5:8150940-8151300	A549	lung:	n/a	chr5:8151114-8151125
26	CEBPB	chr5:8176175-8176647	ECC-1	luminal epithelium:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
27	CEBPB	chr5:8176205-8176610	A549	lung:	n/a	chr5:8176414-8176425 chr5:8176416-8176425 chr5:8176416-8176425 chr5:8176414-8176427 chr5:8176416-8176425 chr5:8176416-8176425
28	CEBPB	chr5:8177836-8178084	A549	lung:	n/a	chr5:8177973-8177986
29	CEBPB	chr5:8138567-8138790	A549	lung:	n/a	chr5:8138707-8138718
30	CEBPB	chr5:8171355-8171673	HepG2	liver:	n/a	chr5:8171506-8171515 chr5:8171504-8171515 chr5:8171505-8171516
31	CEBPB	chr5:8165153-8165357	HepG2	liver:	n/a	chr5:8165244-8165255
32	CTCF	chr5:8184671-8184882	NHEK	skin:	n/a	chr5:8184770-8184779
33	CTCF	chr5:8184678-8184915	Lung_OC	lung:	n/a	chr5:8184770-8184779
34	CTCF	chr5:8184619-8184929	Gliobla	brain:	n/a	chr5:8184770-8184779
35	CTCF	chr5:8184680-8184830	HCT-116	colon:	n/a	chr5:8184770-8184779
36	CTCF	chr5:8184649-8184914	ProgFib	skin:	n/a	chr5:8184770-8184779
37	CTCF	chr5:8184740-8184890	GM12866	blood:	n/a	chr5:8184770-8184779
38	CTCF	chr5:8184671-8184918	LNCaP	prostate:	n/a	chr5:8184770-8184779
39	CTCF	chr5:8184700-8184850	HRPEpiC	eye:	n/a	chr5:8184770-8184779
40	CTCF	chr5:8184700-8184850	HFF-Myc	foreskin:	n/a	chr5:8184770-8184779
41	CTCF	chr5:8184760-8184910	NHLF	lung:	n/a	chr5:8184770-8184779
42	CTCF	chr5:8184558-8184867	K562	blood:	n/a	chr5:8184770-8184779
43	CTCF	chr5:8184700-8184850	Hela-S3	cervix:	n/a	chr5:8184770-8184779
44	CTCF	chr5:8184740-8184890	GM12867	blood:	n/a	chr5:8184770-8184779
45	CTCF	chr5:8184674-8184885	Hela-S3	cervix:	n/a	chr5:8184770-8184779
46	CTCF	chr5:8184540-8184690	A549	lung:	n/a	n/a
47	CTCF	chr5:8184740-8184890	HFF	foreskin:	n/a	chr5:8184770-8184779
48	CTCF	chr5:8184638-8184910	MCF-7	breast:	n/a	chr5:8184770-8184779
49	CTCF	chr5:8184720-8184870	BE2_C	brain:	n/a	chr5:8184770-8184779
50	CTCF	chr5:8184700-8184850	WERI-Rb-1	eye:	n/a	chr5:8184770-8184779

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:8181808..8184211-chr5:8185968..8188351,2	K562	blood:
2	chr5:8181808..8184211-chr5:8185968..8188351,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FASTKD3-4	chr5:8157654-8157901	NONHSAT100281

Variant related genes	Relation type
ENSG00000249486	TF binding region

Extended variants
information (count: 1051 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1051 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79487605	chr5:8138428-8138429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527456622	chr5:8138488-8138489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567824546	chr5:8138500-8138501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78901387	chr5:8138537-8138538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561127781	chr5:8138539-8138540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147944309	chr5:8138581-8138582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141743049	chr5:8144818-8144819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs336141	chr5:8144869-8144870	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs527832698	chr5:8144884-8144885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548077415	chr5:8144924-8144925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184107488	chr5:8144955-8144956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs72729762	chr5:8144981-8144982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532282320	chr5:8145007-8145008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146022040	chr5:8145011-8145012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs386685234	chr5:8145014-8145015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs336140	chr5:8145022-8145023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201132249	chr5:8145039-8145040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558640303	chr5:8145054-8145055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189233146	chr5:8145167-8145168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534557585	chr5:8145181-8145182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138826531	chr5:8145196-8145197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574671387	chr5:8145255-8145256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143152366	chr5:8145277-8145278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs16879943	chr5:8145306-8145307	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs560236741	chr5:8145312-8145313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575997932	chr5:8145349-8145350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545099561	chr5:8145365-8145366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147473182	chr5:8145372-8145373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs527775362	chr5:8145426-8145427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs139256115	chr5:8145452-8145453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561519366	chr5:8145493-8145494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530344579	chr5:8145513-8145514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs386685235	chr5:8145587-8145588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs199760101	chr5:8145588-8145589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552156095	chr5:8145591-8145592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs35439463	chr5:8145607-8145608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532104507	chr5:8145618-8145619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377618162	chr5:8145619-8145620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370928120	chr5:8145649-8145650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534692231	chr5:8145657-8145658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192148649	chr5:8145668-8145669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs115917229	chr5:8145702-8145703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115361083	chr5:8145765-8145766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556788393	chr5:8145784-8145785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs72729765	chr5:8151040-8151041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185230035	chr5:8151052-8151053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs336158	chr5:8151082-8151083	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs549837126	chr5:8151163-8151164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148438157	chr5:8151199-8151200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7723051	chr5:8151217-8151218	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance

Variant related diseases (count:99)

Disease	PMID	Source
Lung cancer	21911935	CNVD
Cri-du chat syndrome	21549014	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Ovarian cancer	19193619	CNVD
Hepatocellular carcinoma	16785998	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:8138200-8138600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr5:8144800-8145800	Enhancers	Fetal Lung	lung
3	chr5:8145200-8145600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:8151000-8151600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr5:8151000-8151800	Enhancers	Brain Cingulate Gyrus	brain
6	chr5:8151200-8151600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:8157600-8158400	Weak transcription	Spleen	Spleen
8	chr5:8158400-8158600	Enhancers	Spleen	Spleen
9	chr5:8159800-8160000	Enhancers	H9 Cell Line	embryonic stem cell
10	chr5:8166000-8166200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:8166200-8166400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr5:8166200-8166600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr5:8166200-8166800	ZNF genes & repeats	Pancreas	Pancrea
14	chr5:8166400-8166600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:8166800-8180800	Weak transcription	Pancreas	Pancrea
16	chr5:8172600-8173600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:8173600-8174800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr5:8175000-8175200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr5:8176000-8176400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr5:8176000-8176600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr5:8176200-8176400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr5:8176200-8176400	Enhancers	Gastric	stomach
23	chr5:8176200-8176800	Enhancers	Ovary	ovary
24	chr5:8176400-8180800	Weak transcription	Gastric	stomach
25	chr5:8176600-8188200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr5:8180200-8181600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr5:8180400-8181400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr5:8180600-8181400	Enhancers	H1 Cell Line	embryonic stem cell
29	chr5:8180800-8181200	Enhancers	Gastric	stomach
30	chr5:8180800-8181400	Enhancers	H9 Cell Line	embryonic stem cell
31	chr5:8180800-8181400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr5:8180800-8181400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr5:8180800-8181400	Enhancers	Pancreas	Pancrea
34	chr5:8180800-8181600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr5:8181000-8181400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr5:8181000-8181400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr5:8181200-8181600	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr5:8181400-8189400	Weak transcription	Pancreas	Pancrea
39	chr5:8181600-8182600	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr5:8182600-8183200	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr5:8186400-8187000	Enhancers	Fetal Brain Male	brain
42	chr5:8188200-8188400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr5:8188400-8188800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr5:8188800-8190000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr5:8189000-8189600	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr5:8189000-8190000	Enhancers	Dnd41	blood
47	chr5:8189200-8190000	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr5:8189400-8190000	Enhancers	Pancreas	Pancrea
49	chr5:8192400-8193400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
50	chr5:8193000-8193400	Enhancers	Primary hematopoietic stem cells short term culture	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links