Variant report

Variant	esv3408069
Chromosome Location	chr15:59902285-59904833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:86)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:86 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:59903791-59904170	HepG2	liver:	n/a	n/a
2	BCL3	chr15:59903393-59904359	A549	lung:	n/a	n/a
3	BHLHE40	chr15:59903850-59904160	HepG2	liver:	n/a	n/a
4	BRCA1	chr15:59903860-59904120	Hela-S3	cervix:	n/a	n/a
5	CHD2	chr15:59903897-59904106	HepG2	liver:	n/a	n/a
6	CHD2	chr15:59903849-59904022	Hela-S3	cervix:	n/a	n/a
7	ELF1	chr15:59903631-59904270	A549	lung:	n/a	n/a
8	ELK1	chr15:59904071-59904206	Hela-S3	cervix:	n/a	n/a
9	EP300	chr15:59903865-59904262	HepG2	liver:	n/a	n/a
10	EP300	chr15:59903437-59904482	A549	lung:	n/a	n/a
11	EP300	chr15:59903808-59904227	HepG2	liver:	n/a	n/a
12	EP300	chr15:59903540-59904445	A549	lung:	n/a	n/a
13	EP300	chr15:59903963-59904251	HepG2	liver:	n/a	n/a
14	ETS1	chr15:59903674-59904295	A549	lung:	n/a	chr15:59904136-59904151
15	FOS	chr15:59903855-59904176	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr15:59903872-59904160	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr15:59903843-59904186	MCF10A-Er-Src	breast:	n/a	n/a
18	FOSL2	chr15:59903499-59904609	A549	lung:	n/a	n/a
19	FOSL2	chr15:59903638-59904267	A549	lung:	n/a	n/a
20	FOSL2	chr15:59903834-59904203	HepG2	liver:	n/a	n/a
21	FOXA1	chr15:59903828-59904204	HepG2	liver:	n/a	n/a
22	FOXA1	chr15:59903826-59904101	HepG2	liver:	n/a	n/a
23	FOXA1	chr15:59903761-59904104	HepG2	liver:	n/a	n/a
24	FOXA1	chr15:59903815-59904134	HepG2	liver:	n/a	n/a
25	FOXA2	chr15:59903771-59904070	HepG2	liver:	n/a	n/a
26	FOXA2	chr15:59903833-59904261	A549	lung:	n/a	n/a
27	FOXA2	chr15:59903671-59904270	A549	lung:	n/a	n/a
28	GABPA	chr15:59903547-59904481	A549	lung:	n/a	n/a
29	GATA3	chr15:59903530-59904582	A549	lung:	n/a	n/a
30	HEY1	chr15:59903852-59904139	HepG2	liver:	n/a	n/a
31	JUN	chr15:59903859-59904083	HepG2	liver:	n/a	n/a
32	JUND	chr15:59903793-59904252	A549	lung:	n/a	chr15:59903978-59903989
33	JUND	chr15:59903788-59904305	A549	lung:	n/a	chr15:59903978-59903989
34	JUND	chr15:59903800-59904105	HepG2	liver:	n/a	chr15:59903978-59903989
35	MAFF	chr15:59903851-59904293	HepG2	liver:	n/a	chr15:59904039-59904057
36	MAFK	chr15:59903865-59904234	Hela-S3	cervix:	n/a	chr15:59904045-59904056 chr15:59904043-59904057 chr15:59904045-59904056 chr15:59904040-59904055 chr15:59904044-59904055 chr15:59904044-59904055
37	MAFK	chr15:59903835-59904297	HepG2	liver:	n/a	chr15:59904045-59904056 chr15:59904043-59904057 chr15:59904045-59904056 chr15:59904040-59904055 chr15:59904044-59904055 chr15:59904044-59904055
38	MAFK	chr15:59903787-59904226	HepG2	liver:	n/a	chr15:59904045-59904056 chr15:59904043-59904057 chr15:59904045-59904056 chr15:59904040-59904055 chr15:59904044-59904055 chr15:59904044-59904055
39	MAX	chr15:59903663-59904409	A549	lung:	n/a	n/a
40	MAX	chr15:59903894-59904125	Hela-S3	cervix:	n/a	n/a
41	MAX	chr15:59903526-59905298	A549	lung:	n/a	n/a
42	POLR2A	chr15:59903911-59904194	A549	lung:	n/a	n/a
43	POLR2A	chr15:59904596-59905146	A549	lung:	n/a	n/a
44	POLR2A	chr15:59903943-59904131	HepG2	liver:	n/a	n/a
45	POLR2A	chr15:59904770-59905036	A549	lung:	n/a	n/a
46	POLR2A	chr15:59903804-59904245	HepG2	liver:	n/a	n/a
47	POLR2A	chr15:59903752-59904211	HepG2	liver:	n/a	n/a
48	POLR2A	chr15:59904762-59905064	A549	lung:	n/a	n/a
49	POLR2A	chr15:59903933-59904195	A549	lung:	n/a	n/a
50	POLR2A	chr15:59904832-59905037	A549	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:59904009-59904059	ovcar-3	ovarian:	n/a
2	chr15:59904009-59904059	GM06990	blood:	n/a
3	chr15:59904009-59904059	PFSK-1	brain:	n/a
4	chr15:59904009-59904059	AG04449	skin:	fetal
5	chr15:59903968-59904018	ProgFib	skin:	n/a
6	chr15:59903968-59904018	Caco-2	colon:	n/a
7	chr15:59904009-59904059	AG09309	skin:	n/a
8	chr15:59903968-59904018	AG09309	skin:	n/a
9	chr15:59904009-59904059	IMR90	lung:	fetal
10	chr15:59904009-59904059	HIPEpiC	eye:	n/a
11	chr15:59903968-59904018	Hepatocyte	liver:	n/a
12	chr15:59903968-59904018	HMEC	breast:	n/a
13	chr15:59904009-59904059	Hela-S3	cervix:	n/a
14	chr15:59903968-59904018	HepG2	liver:	n/a
15	chr15:59904009-59904059	NT2-D1	testis:	n/a
16	chr15:59904009-59904059	A549	lung:	n/a
17	chr15:59904009-59904059	HCPEpiC	choroid plexus:	n/a
18	chr15:59904009-59904059	SAEC	small airway:	n/a
19	chr15:59904009-59904059	U87	brain:	n/a
20	chr15:59904009-59904059	HEEpiC	esophagus:	n/a
21	chr15:59903968-59904018	AG10803	skin:	n/a
22	chr15:59903968-59904018	NHBE	bronchial:	n/a
23	chr15:59903968-59904018	HCT-116	colon:	n/a
24	chr15:59904009-59904059	HCT-116	colon:	n/a
25	chr15:59904009-59904059	H1-hESC	embryonic stem cell:	embryo
26	chr15:59903968-59904018	HEK293	kidney:	embryo
27	chr15:59903968-59904018	MCF10A-Er-Src	breast:	n/a
28	chr15:59903968-59904018	HIPEpiC	eye:	n/a
29	chr15:59904009-59904059	MCF-7	breast:	n/a
30	chr15:59904009-59904059	HMEC	breast:	n/a
31	chr15:59903968-59904018	ovcar-3	ovarian:	n/a
32	chr15:59904009-59904059	HNPCEpiC	eye:	n/a
33	chr15:59903968-59904018	GM12878	blood:	n/a
34	chr15:59903968-59904018	BJ	skin:	n/a
35	chr15:59904009-59904059	NHDF-neo	bronchial:	n/a
36	chr15:59903968-59904018	GM12892	blood:	n/a
37	chr15:59903968-59904018	K562	blood:	n/a
38	chr15:59904009-59904059	SK-N-SH	brain:	n/a
39	chr15:59904009-59904059	K562	blood:	n/a
40	chr15:59903968-59904018	HCF	heart:	n/a
41	chr15:59904009-59904059	HAEpiC	amniotic membrane:	n/a
42	chr15:59904009-59904059	AG10803	skin:	n/a
43	chr15:59904009-59904059	AG04450	lung:	fetal
44	chr15:59903968-59904018	BE2_C	brain:	n/a
45	chr15:59903968-59904018	PANC-1	pancreas:	n/a
46	chr15:59904009-59904059	MCF10A-Er-Src	breast:	n/a
47	chr15:59903968-59904018	SK-N-SH	brain:	n/a
48	chr15:59903968-59904018	HEEpiC	esophagus:	n/a
49	chr15:59903968-59904018	GM06990	blood:	n/a
50	chr15:59903968-59904018	SAEC	small airway:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:59891038..59893878-chr15:59903015..59906504,3	K562	blood:
2	chr15:59885738..59888481-chr15:59900504..59902552,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GCNT3-2	chr15:59904101-59904180	NONHSAT044179
2	lnc-GCNT3-2	chr15:59904101-59904180	NONHSAT044178
3	lnc-GCNT3-2	chr15:59904101-59904180	NONHSAT044180
4	lnc-GCNT3-2	chr15:59903591-59903875	NONHSAT044181

No data

Variant related genes	Relation type
GCNT3	TF binding region
GCNT3	CpG island
ENSG00000140297	chromatin interactions

Extended variants
information (count: 176 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:176 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72751130	chr15:59902306-59902307	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560100078	chr15:59902347-59902348	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs111731814	chr15:59902368-59902369	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs146959228	chr15:59902380-59902381	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs138002798	chr15:59902384-59902385	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183485410	chr15:59902388-59902389	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189028300	chr15:59902392-59902393	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs193150243	chr15:59902396-59902397	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs11852635	chr15:59902400-59902401	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs183560519	chr15:59902404-59902405	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs188295235	chr15:59902408-59902409	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs191347040	chr15:59902412-59902413	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs183875159	chr15:59902416-59902417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs189583470	chr15:59902420-59902421	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs181631929	chr15:59902424-59902425	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs563239044	chr15:59902426-59902427	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs143890911	chr15:59902453-59902454	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs148687268	chr15:59902454-59902455	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs376692390	chr15:59902455-59902456	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs34582957	chr15:59902461-59902462	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567298832	chr15:59902470-59902471	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs534579753	chr15:59902473-59902474	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs546527238	chr15:59902474-59902475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs550340216	chr15:59902482-59902483	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs34750594	chr15:59902486-59902487	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371319392	chr15:59902497-59902498	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570124330	chr15:59902562-59902563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34727338	chr15:59902564-59902565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375312224	chr15:59902565-59902566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs386784501	chr15:59902567-59902568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368721291	chr15:59902592-59902593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369700648	chr15:59902593-59902594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552263040	chr15:59902611-59902612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566381559	chr15:59902614-59902615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535043253	chr15:59902618-59902619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146235092	chr15:59902662-59902663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149319736	chr15:59902691-59902692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142261083	chr15:59902701-59902702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139311306	chr15:59902710-59902711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186929744	chr15:59902718-59902719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190612362	chr15:59902730-59902731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545003812	chr15:59902738-59902739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371114737	chr15:59902762-59902763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373616626	chr15:59902774-59902775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556990967	chr15:59902789-59902790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs367753139	chr15:59902794-59902795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371544409	chr15:59902806-59902807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182001320	chr15:59902834-59902835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374078359	chr15:59902837-59902838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536795539	chr15:59902854-59902855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Mental retardation	17124404	CNVD
Gastrointestinal stromal cancer	20877625	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59896800-59911800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr15:59897400-59903400	Weak transcription	HepG2	liver
3	chr15:59902000-59902400	Enhancers	Duodenum Mucosa	Duodenum
4	chr15:59902000-59902400	ZNF genes & repeats	A549	lung
5	chr15:59902200-59903400	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr15:59902200-59903600	Weak transcription	Pancreas	Pancrea
7	chr15:59902200-59903600	Weak transcription	Stomach Mucosa	stomach
8	chr15:59902200-59905000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr15:59902400-59903400	Weak transcription	A549	lung
10	chr15:59902400-59903600	Weak transcription	Duodenum Mucosa	Duodenum
11	chr15:59902800-59904200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr15:59903000-59903200	Active TSS	HSMM	muscle
13	chr15:59903200-59903600	Flanking Active TSS	HSMM	muscle
14	chr15:59903400-59903600	Enhancers	Fetal Intestine Small	intestine
15	chr15:59903400-59903600	Active TSS	Rectal Mucosa Donor 31	rectum
16	chr15:59903400-59903600	Enhancers	Hela-S3	cervix
17	chr15:59903400-59903600	Enhancers	HepG2	liver
18	chr15:59903400-59903800	Flanking Active TSS	A549	lung
19	chr15:59903400-59905600	Enhancers	Fetal Intestine Large	intestine
20	chr15:59903600-59903800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr15:59903600-59903800	Enhancers	Colonic Mucosa	Colon
22	chr15:59903600-59903800	Flanking Active TSS	Fetal Intestine Small	intestine
23	chr15:59903600-59903800	Flanking Active TSS	NHDF-Ad	bronchial
24	chr15:59903600-59904000	Enhancers	Liver	Liver
25	chr15:59903600-59904000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr15:59903600-59904200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr15:59903600-59904200	Active TSS	Rectal Mucosa Donor 29	rectum
28	chr15:59903600-59904400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
29	chr15:59903600-59904400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:59903600-59904400	Enhancers	Pancreas	Pancrea
31	chr15:59903600-59904400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
32	chr15:59903600-59904400	Flanking Active TSS	Hela-S3	cervix
33	chr15:59903600-59905000	Active TSS	Rectal Smooth Muscle	rectum
34	chr15:59903600-59905200	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr15:59903600-59905200	Flanking Active TSS	HepG2	liver
36	chr15:59903600-59905400	Active TSS	Stomach Mucosa	stomach
37	chr15:59903600-59907200	Active TSS	Duodenum Mucosa	Duodenum
38	chr15:59903800-59904000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
39	chr15:59903800-59904000	Weak transcription	Fetal Intestine Small	intestine
40	chr15:59903800-59904200	Weak transcription	Colonic Mucosa	Colon
41	chr15:59903800-59904200	Enhancers	NHDF-Ad	bronchial
42	chr15:59903800-59905000	Active TSS	A549	lung
43	chr15:59904000-59904400	Enhancers	Osteobl	bone
44	chr15:59904000-59905000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
45	chr15:59904000-59906000	ZNF genes & repeats	Fetal Intestine Small	intestine
46	chr15:59904200-59904400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr15:59904200-59904600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
48	chr15:59904200-59904800	Active TSS	Gastric	stomach
49	chr15:59904200-59905200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr15:59904200-59905200	Active TSS	Fetal Stomach	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links