Variant report

Variant	nsv880239
Chromosome Location	chr4:147666797-147779999
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	BACH1	chr4:147772024-147772068	K562	blood:	n/a	n/a
2	BCL3	chr4:147768074-147768335	GM12878	blood:	n/a	chr4:147768267-147768276 chr4:147768266-147768275
3	CEBPB	chr4:147702358-147702612	A549	lung:	n/a	chr4:147702460-147702473 chr4:147702460-147702471 chr4:147702570-147702583 chr4:147702460-147702473
4	CEBPB	chr4:147702310-147702597	IMR90	lung:	n/a	chr4:147702460-147702473 chr4:147702460-147702471 chr4:147702570-147702583 chr4:147702460-147702473
5	CEBPB	chr4:147688387-147688463	HepG2	liver:	n/a	chr4:147688415-147688426
6	CEBPB	chr4:147755904-147756203	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:147702326-147702760	HepG2	liver:	n/a	chr4:147702728-147702741 chr4:147702460-147702473 chr4:147702460-147702471 chr4:147702570-147702583 chr4:147702460-147702473
8	CEBPB	chr4:147755914-147756159	K562	blood:	n/a	n/a
9	CEBPB	chr4:147755844-147756202	IMR90	lung:	n/a	n/a
10	CEBPB	chr4:147690666-147691017	HepG2	liver:	n/a	chr4:147690858-147690871 chr4:147690858-147690869 chr4:147690860-147690869 chr4:147690761-147690774
11	CEBPB	chr4:147712732-147712919	HepG2	liver:	n/a	chr4:147712780-147712791
12	CEBPB	chr4:147685317-147685488	IMR90	lung:	n/a	chr4:147685398-147685411 chr4:147685399-147685410 chr4:147685398-147685411 chr4:147685398-147685409
13	CEBPB	chr4:147685334-147685532	HepG2	liver:	n/a	chr4:147685398-147685411 chr4:147685399-147685410 chr4:147685398-147685411 chr4:147685398-147685409
14	CEBPB	chr4:147690685-147690997	IMR90	lung:	n/a	chr4:147690858-147690871 chr4:147690858-147690869 chr4:147690860-147690869 chr4:147690761-147690774
15	CEBPB	chr4:147755880-147756166	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr4:147742206-147742390	K562	blood:	n/a	n/a
17	CEBPB	chr4:147690701-147691038	A549	lung:	n/a	chr4:147690858-147690871 chr4:147690858-147690869 chr4:147690860-147690869 chr4:147690761-147690774
18	CEBPB	chr4:147702380-147702524	K562	blood:	n/a	chr4:147702460-147702473 chr4:147702460-147702471 chr4:147702460-147702473
19	CEBPB	chr4:147755875-147756151	A549	lung:	n/a	n/a
20	CEBPB	chr4:147764560-147764785	HepG2	liver:	n/a	n/a
21	CTCF	chr4:147763474-147763529	GM13976	blood:	n/a	n/a
22	CTCF	chr4:147688621-147688632	GM20000	blood:	n/a	n/a
23	CTCF	chr4:147706210-147706253	GM13976	blood:	n/a	n/a
24	CTCF	chr4:147770197-147770236	Fibrobl	skin:	n/a	n/a
25	CTCF	chr4:147757100-147757250	MCF-7	breast:	n/a	n/a
26	CTCF	chr4:147720246-147720323	GM20000	blood:	n/a	n/a
27	E2F4	chr4:147751338-147751675	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr4:147711883-147712051	MCF10A-Er-Src	breast:	n/a	n/a
29	EP300	chr4:147694851-147694912	K562	blood:	n/a	n/a
30	FOS	chr4:147764544-147764743	MCF10A-Er-Src	breast:	n/a	chr4:147764592-147764604 chr4:147764594-147764602 chr4:147764594-147764603 chr4:147764594-147764601
31	FOS	chr4:147701379-147701560	MCF10A-Er-Src	breast:	n/a	chr4:147701420-147701427 chr4:147701428-147701440 chr4:147701419-147701428 chr4:147701418-147701428 chr4:147701419-147701427
32	FOS	chr4:147721346-147721368	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr4:147711715-147712023	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr4:147714698-147715063	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr4:147711753-147711968	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr4:147764464-147764664	MCF10A-Er-Src	breast:	n/a	chr4:147764592-147764604 chr4:147764594-147764602 chr4:147764594-147764603 chr4:147764594-147764601
37	FOS	chr4:147715921-147715930	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr4:147764465-147764719	MCF10A-Er-Src	breast:	n/a	chr4:147764592-147764604 chr4:147764594-147764602 chr4:147764594-147764603 chr4:147764594-147764601
39	FOS	chr4:147711696-147712004	MCF10A-Er-Src	breast:	n/a	n/a
40	GABPA	chr4:147735818-147735935	HepG2	liver:	n/a	n/a
41	GABPA	chr4:147735773-147735885	HepG2	liver:	n/a	n/a
42	GATA2	chr4:147736563-147736804	SH-SY5Y	brain:	n/a	n/a
43	GATA2	chr4:147683299-147683799	SH-SY5Y	brain:	n/a	chr4:147683509-147683519
44	GATA3	chr4:147683381-147683854	SH-SY5Y	brain:	n/a	chr4:147683509-147683519 chr4:147683794-147683805
45	GATA3	chr4:147684674-147685044	SH-SY5Y	brain:	n/a	chr4:147684756-147684766
46	GATA3	chr4:147755435-147755908	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr4:147736642-147737085	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr4:147761191-147761368	SH-SY5Y	brain:	n/a	n/a
49	JUN	chr4:147702381-147702444	HepG2	liver:	n/a	n/a
50	JUN	chr4:147744294-147744361	HepG2	liver:	n/a	chr4:147744315-147744328

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:147732398-147732448	LNCaP	prostate:	n/a
2	chr4:147732398-147732448	ovcar-3	ovarian:	n/a
3	chr4:147732398-147732448	MCF-7	breast:	n/a
4	chr4:147732398-147732448	PrEC	prostate:	n/a
5	chr4:147732398-147732448	HNPCEpiC	eye:	n/a
6	chr4:147732398-147732448	BE2_C	brain:	n/a
7	chr4:147732398-147732448	HIPEpiC	eye:	n/a
8	chr4:147732398-147732448	AoSMC	blood vessel:	n/a
9	chr4:147732398-147732448	PANC-1	pancreas:	n/a
10	chr4:147732398-147732448	HRPEpiC	eye:	n/a
11	chr4:147732398-147732448	HCT-116	colon:	n/a
12	chr4:147732398-147732448	Hela-S3	cervix:	n/a
13	chr4:147732398-147732448	HEEpiC	esophagus:	n/a
14	chr4:147732398-147732448	AG09319	gingival:	n/a
15	chr4:147732398-147732448	HAEpiC	amniotic membrane:	n/a
16	chr4:147732398-147732448	GM19239	blood:	n/a
17	chr4:147732398-147732448	HUVEC	blood vessel:	n/a
18	chr4:147732398-147732448	NH-A	brain:	n/a
19	chr4:147732398-147732448	IMR90	lung:	fetal
20	chr4:147732398-147732448	HRE	kidney:	n/a
21	chr4:147732398-147732448	HMEC	breast:	n/a
22	chr4:147732398-147732448	BJ	skin:	n/a
23	chr4:147732398-147732448	U87	brain:	n/a
24	chr4:147732398-147732448	NHBE	bronchial:	n/a
25	chr4:147732398-147732448	SK-N-SH	brain:	n/a
26	chr4:147732398-147732448	HCPEpiC	choroid plexus:	n/a
27	chr4:147732398-147732448	H1-hESC	embryonic stem cell:	embryo
28	chr4:147732398-147732448	ProgFib	skin:	n/a
29	chr4:147732398-147732448	HPAEpiC	pulmonary alveolar:	n/a
30	chr4:147732398-147732448	GM12892	blood:	n/a
31	chr4:147732398-147732448	AG04449	skin:	fetal
32	chr4:147732398-147732448	A549	lung:	n/a
33	chr4:147732398-147732448	AG10803	skin:	n/a
34	chr4:147732398-147732448	NB4	blood:	n/a
35	chr4:147732398-147732448	AG09309	skin:	n/a
36	chr4:147732398-147732448	GM06990	blood:	n/a
37	chr4:147732398-147732448	PFSK-1	brain:	n/a
38	chr4:147732398-147732448	RPTEC	kidney:	n/a
39	chr4:147732398-147732448	HCF	heart:	n/a
40	chr4:147732398-147732448	SAEC	small airway:	n/a
41	chr4:147732398-147732448	AG04450	lung:	fetal
42	chr4:147732398-147732448	SKMC	muscle:	n/a
43	chr4:147732398-147732448	SK-N-MC	brain:	n/a
44	chr4:147732398-147732448	MCF10A-Er-Src	breast:	n/a
45	chr4:147732398-147732448	GM12891	blood:	n/a
46	chr4:147732398-147732448	GM12878	blood:	n/a
47	chr4:147732398-147732448	ECC-1	luminal epithelium:	n/a
48	chr4:147732398-147732448	HepG2	liver:	n/a
49	chr4:147732398-147732448	NHDF-neo	bronchial:	n/a
50	chr4:147732398-147732448	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:147700024..147702525-chr4:147717625..147719215,2	K562	blood:
2	chr4:147684151..147686081-chr4:147690285..147692908,2	K562	blood:
3	chr4:147700024..147702525-chr4:147717625..147719215,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC10A7-4	chr4:147733909-147734182	NONHSAT098675
2	lnc-SLC10A7-4	chr4:147724628-147724837	NONHSAT098675
3	lnc-SLC10A7-3	chr4:147684966-147685339	NONHSAT098674

Variant related genes	Relation type
TTC29	TF binding region
TTC29	CpG island
ENSG00000137473	chromatin interactions

Extended variants
information (count: 1690 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1690 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141746461	chr4:147668419-147668420	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs180760155	chr4:147668426-147668427	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs564135272	chr4:147668485-147668486	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs185201354	chr4:147668508-147668509	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs62328015	chr4:147668513-147668514	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs190067121	chr4:147668522-147668523	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs565639156	chr4:147668572-147668573	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs528242244	chr4:147668596-147668597	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs548377744	chr4:147668597-147668598	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs150530686	chr4:147668625-147668626	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs139535122	chr4:147668642-147668643	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs149664313	chr4:147668661-147668662	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs147365274	chr4:147668672-147668673	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs114449556	chr4:147668765-147668766	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs181344010	chr4:147668777-147668778	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs552180142	chr4:147668799-147668800	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs576064806	chr4:147668900-147668901	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs373222789	chr4:147668972-147668973	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs573497259	chr4:147668975-147668976	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs186768983	chr4:147668990-147668991	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs139461184	chr4:147669001-147669002	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs371078047	chr4:147669006-147669007	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs144887925	chr4:147669008-147669009	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs561761964	chr4:147669020-147669021	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs544289136	chr4:147669106-147669107	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs147962212	chr4:147669116-147669117	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs191611014	chr4:147669120-147669121	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs540252501	chr4:147669137-147669138	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs183908873	chr4:147669157-147669158	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs528367864	chr4:147669158-147669159	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs200394595	chr4:147669172-147669173	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs548238063	chr4:147669203-147669204	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs528591244	chr4:147669205-147669206	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs568240025	chr4:147669261-147669262	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs530629662	chr4:147669287-147669288	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs148974964	chr4:147669308-147669309	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs546730836	chr4:147669323-147669324	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs13145411	chr4:147669420-147669421	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs570583656	chr4:147669424-147669425	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs539407318	chr4:147669436-147669437	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs552989491	chr4:147669441-147669442	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs566372349	chr4:147669442-147669443	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs113157428	chr4:147669479-147669480	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs78303147	chr4:147669496-147669497	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs575752913	chr4:147669544-147669545	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs546036878	chr4:147675610-147675611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559390486	chr4:147675612-147675613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528259149	chr4:147675634-147675635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111964694	chr4:147675679-147675680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139430167	chr4:147675777-147675778	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21633010	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147668400-147669600	ZNF genes & repeats	Spleen	Spleen
2	chr4:147675600-147676000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:147682800-147683800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:147698000-147698200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:147706600-147708600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr4:147708600-147709000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:147708600-147709400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:147708800-147709400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:147708800-147709600	Enhancers	Brain Germinal Matrix	brain
10	chr4:147711600-147712200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:147711600-147712200	Enhancers	NHEK	skin
12	chr4:147711800-147712200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:147711800-147712400	Enhancers	HMEC	breast
14	chr4:147712200-147714600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:147714600-147715200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:147734000-147737600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:147736000-147736400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr4:147737600-147737800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr4:147737600-147737800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:147737800-147748200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr4:147748200-147748400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:147748400-147753600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr4:147753600-147753800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr4:147764600-147764800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr4:147764800-147773600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:147765400-147766000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr4:147765800-147766200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr4:147765800-147766400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:147765800-147766400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr4:147765800-147767000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr4:147766000-147766400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr4:147766400-147779400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:147773600-147773800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links