Variant report

Variant	nsv888655
Chromosome Location	chr7:85178080-85566769
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2257)
CpG islands
(count:0)
Chromatin interactive
region (count:38)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2257 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:85553404-85553749	HepG2	liver:	n/a	chr7:85553645-85553661
2	ARID3A	chr7:85481010-85481241	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:85519598-85519867	K562	blood:	n/a	n/a
4	ARID3A	chr7:85183644-85184017	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:85194316-85194431	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:85519578-85519866	HepG2	liver:	n/a	n/a
7	ATF1	chr7:85210707-85210842	K562	blood:	n/a	n/a
8	ATF1	chr7:85183590-85183761	K562	blood:	n/a	n/a
9	ATF2	chr7:85435728-85435968	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr7:85324800-85325257	A549	lung:	n/a	n/a
11	ATF3	chr7:85324945-85325334	A549	lung:	n/a	n/a
12	BACH1	chr7:85229703-85230012	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:85467218-85467232	K562	blood:	n/a	n/a
14	BACH1	chr7:85362473-85362491	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr7:85343575-85343840	GM12878	blood:	n/a	n/a
16	BCL3	chr7:85221189-85221679	A549	lung:	n/a	n/a
17	BCL3	chr7:85349735-85350327	A549	lung:	n/a	n/a
18	BCL3	chr7:85324797-85325464	A549	lung:	n/a	n/a
19	BHLHE40	chr7:85183697-85183834	K562	blood:	n/a	n/a
20	BHLHE40	chr7:85221305-85221476	HepG2	liver:	n/a	n/a
21	BHLHE40	chr7:85343571-85343913	GM12878	blood:	n/a	n/a
22	BRCA1	chr7:85481061-85481193	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr7:85363774-85363793	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr7:85349322-85349783	Hela-S3	cervix:	n/a	n/a
25	CCNT2	chr7:85231581-85231835	K562	blood:	n/a	n/a
26	CEBPB	chr7:85441740-85442067	HepG2	liver:	n/a	n/a
27	CEBPB	chr7:85349420-85349797	A549	lung:	n/a	n/a
28	CEBPB	chr7:85324852-85325324	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr7:85184148-85184492	HepG2	liver:	n/a	chr7:85184415-85184426 chr7:85184308-85184321 chr7:85184309-85184320 chr7:85184415-85184428 chr7:85184415-85184426
30	CEBPB	chr7:85458553-85458817	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr7:85178678-85178883	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:85480914-85481089	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr7:85277974-85278295	IMR90	lung:	n/a	chr7:85278124-85278135
34	CEBPB	chr7:85251491-85251687	A549	lung:	n/a	n/a
35	CEBPB	chr7:85324745-85325466	A549	lung:	n/a	n/a
36	CEBPB	chr7:85469817-85470187	IMR90	lung:	n/a	chr7:85469981-85469992 chr7:85469980-85469993 chr7:85469980-85469993
37	CEBPB	chr7:85329881-85330071	H1-hESC	embryonic stem cell:	n/a	chr7:85330002-85330013
38	CEBPB	chr7:85458569-85458814	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr7:85482881-85483081	HepG2	liver:	n/a	n/a
40	CEBPB	chr7:85270485-85270737	HepG2	liver:	n/a	chr7:85270598-85270609
41	CEBPB	chr7:85469881-85470132	HepG2	liver:	n/a	chr7:85469981-85469992 chr7:85469980-85469993 chr7:85469980-85469993
42	CEBPB	chr7:85178686-85178918	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr7:85183580-85183936	IMR90	lung:	n/a	n/a
44	CEBPB	chr7:85183600-85183934	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr7:85349880-85350303	A549	lung:	n/a	n/a
46	CEBPB	chr7:85476685-85476977	HepG2	liver:	n/a	chr7:85476808-85476819
47	CEBPB	chr7:85225271-85225515	IMR90	lung:	n/a	n/a
48	CEBPB	chr7:85332157-85332447	K562	blood:	n/a	chr7:85332259-85332270
49	CEBPB	chr7:85312180-85312451	IMR90	lung:	n/a	n/a
50	CEBPB	chr7:85349350-85350293	A549	lung:	n/a	n/a

No data

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:85183273..85184394-chr7:85379037..85380205,4	MCF-7	breast:
2	chr7:85224212..85226454-chr7:85229348..85230972,2	MCF-7	breast:
3	chr7:85513282..85514931-chr7:85515657..85518081,2	K562	blood:
4	chr7:84670634..84671600-chr7:85379520..85380121,2	MCF-7	breast:
5	chr7:85153959..85156643-chr7:85186340..85188558,2	K562	blood:
6	chr7:85513282..85514931-chr7:85515657..85518081,2	K562	blood:
7	chr7:84659480..84660360-chr7:85183314..85184162,2	MCF-7	breast:
8	chr7:85519463..85520587-chr7:86098657..86099580,4	MCF-7	breast:
9	chr7:84652105..84652692-chr7:85458869..85459474,2	MCF-7	breast:
10	chr7:85522405..85523206-chr7:86098665..86099240,2	MCF-7	breast:
11	chr7:85373526..85376335-chr7:85378810..85381383,2	K562	blood:
12	chr7:85556969..85559949-chr7:85562063..85564200,2	K562	blood:
13	chr7:85315775..85319352-chr7:85321463..85324593,3	K562	blood:
14	chr7:85519420..85520975-chr7:86097643..86099272,2	MCF-7	breast:
15	chr7:84659939..84660879-chr7:85480443..85481564,5	MCF-7	breast:
16	chr7:85308217..85310976-chr7:85319163..85322845,3	K562	blood:
17	chr7:85283178..85285409-chr7:85295868..85298479,2	K562	blood:
18	chr7:84670766..84671527-chr7:85480999..85481548,2	MCF-7	breast:
19	chr7:85393175..85394828-chr7:85402335..85404296,2	K562	blood:
20	chr7:84659852..84660474-chr7:85458932..85459657,2	MCF-7	breast:
21	chr7:85308217..85310976-chr7:85319163..85322845,3	K562	blood:
22	chr12:7024083..7024583-chr7:85192420..85193063,2	MCF-7	breast:
23	chr7:85253799..85255323-chr7:85392933..85394931,2	K562	blood:
24	chr7:85253799..85255323-chr7:85392933..85394931,2	K562	blood:
25	chr7:85518932..85520222-chr7:86098724..86099479,6	MCF-7	breast:
26	chr7:85556969..85559949-chr7:85562063..85564200,2	K562	blood:
27	chr7:84671065..84671572-chr7:85183760..85184324,2	MCF-7	breast:
28	chr7:85183273..85184394-chr7:85379037..85380205,4	MCF-7	breast:
29	chr7:85224212..85226454-chr7:85229348..85230972,2	MCF-7	breast:
30	chr7:84670622..84671190-chr7:85183449..85184130,2	MCF-7	breast:
31	chr7:85315775..85319352-chr7:85321463..85324593,3	K562	blood:
32	chr7:85393175..85394828-chr7:85402335..85404296,2	K562	blood:
33	chr7:85324970..85325867-chr9:91930662..91931441,2	HCT-116	colon:
34	chr7:84670210..84671310-chr7:85458944..85460023,3	MCF-7	breast:
35	chr7:85283178..85285409-chr7:85295868..85298479,2	K562	blood:
36	chr7:85564186..85565687-chr8:22597359..22599914,2	MCF-7	breast:
37	chr7:85373526..85376335-chr7:85378810..85381383,2	K562	blood:
38	chr7:84659833..84660559-chr7:85458909..85459420,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEMA3D-4	chr7:85265329-85265660	NONHSAT121800

No data

Variant related genes	Relation type
ENSG00000227785	TF binding region
ENSG00000153993	chromatin interactions
ENSG00000111674	chromatin interactions

Extended variants
information (count: 7404 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:7404 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371793318	chr7:85178210-85178211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546047099	chr7:85178217-85178218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146776955	chr7:85178243-85178244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534159849	chr7:85178251-85178252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189298126	chr7:85178263-85178264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112417381	chr7:85178339-85178340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs117502642	chr7:85178357-85178358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564237053	chr7:85178376-85178377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531695036	chr7:85178395-85178396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550204040	chr7:85178402-85178403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369186011	chr7:85178465-85178466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186590999	chr7:85178510-85178511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139273565	chr7:85178528-85178529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111327541	chr7:85178535-85178536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190951082	chr7:85178540-85178541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200052939	chr7:85178592-85178593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572812080	chr7:85178593-85178594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570533041	chr7:85178603-85178604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs60204022	chr7:85178604-85178605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529399520	chr7:85178637-85178638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549718215	chr7:85178671-85178672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181645857	chr7:85178697-85178698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547612581	chr7:85178765-85178766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186853690	chr7:85178781-85178782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145293039	chr7:85178813-85178814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1852699	chr7:85178836-85178837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs568886183	chr7:85178843-85178844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530286121	chr7:85178901-85178902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191190863	chr7:85178912-85178913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369456927	chr7:85178943-85178944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73393549	chr7:85178957-85178958	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs567110731	chr7:85178958-85178959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150935468	chr7:85178986-85178987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183107681	chr7:85179001-85179002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558868206	chr7:85179038-85179039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552018254	chr7:85179068-85179069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570024581	chr7:85179077-85179078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111875830	chr7:85179085-85179086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146144403	chr7:85179127-85179128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs3081618	chr7:85179156-85179157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374704833	chr7:85179157-85179158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149083570	chr7:85179161-85179162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555770272	chr7:85179241-85179242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574859874	chr7:85179256-85179257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369373156	chr7:85179272-85179273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78900924	chr7:85179285-85179286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs398005357	chr7:85179287-85179288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189887888	chr7:85179302-85179303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373222967	chr7:85179348-85179349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111409844	chr7:85179356-85179357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:85178200-85180400	Weak transcription	Fetal Lung	lung
2	chr7:85180400-85180600	ZNF genes & repeats	Fetal Lung	lung
3	chr7:85180600-85182400	Weak transcription	Fetal Lung	lung
4	chr7:85182400-85184600	Enhancers	Fetal Lung	lung
5	chr7:85183400-85183800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:85183400-85183800	Enhancers	Fetal Heart	heart
7	chr7:85183400-85184600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr7:85183600-85183800	Enhancers	A549	lung
9	chr7:85183800-85184200	Flanking Active TSS	A549	lung
10	chr7:85184200-85184400	Enhancers	A549	lung
11	chr7:85184600-85193400	Weak transcription	Fetal Lung	lung
12	chr7:85193200-85193400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:85193400-85194000	Enhancers	Placenta Amnion	Placenta Amnion
14	chr7:85193400-85194400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr7:85193400-85195800	Enhancers	Fetal Lung	lung
16	chr7:85194200-85195000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr7:85194200-85196000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr7:85194400-85194800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:85194800-85196800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:85195800-85199600	Weak transcription	Fetal Lung	lung
21	chr7:85196800-85198200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:85198400-85198600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr7:85199600-85201000	Enhancers	Fetal Lung	lung
24	chr7:85201200-85201800	Enhancers	Fetal Kidney	kidney
25	chr7:85202800-85203200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr7:85202800-85204000	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr7:85207600-85208600	Enhancers	Fetal Lung	lung
28	chr7:85208600-85208800	Active TSS	Fetal Lung	lung
29	chr7:85211200-85213000	Enhancers	Placenta Amnion	Placenta Amnion
30	chr7:85212600-85213000	Enhancers	Fetal Heart	heart
31	chr7:85215600-85218000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr7:85216600-85217200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr7:85217000-85217400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr7:85218000-85218200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr7:85221400-85221800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:85221400-85222000	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr7:85221800-85222800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:85222800-85223200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:85222800-85223200	Enhancers	Fetal Intestine Small	intestine
40	chr7:85223200-85223400	Enhancers	Fetal Lung	lung
41	chr7:85223200-85224600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:85224400-85224800	Weak transcription	Fetal Lung	lung
43	chr7:85224600-85225200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:85224800-85225400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr7:85224800-85225800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:85224800-85225800	Enhancers	A549	lung
47	chr7:85225000-85225400	Enhancers	Hela-S3	cervix
48	chr7:85225000-85225400	Enhancers	NHDF-Ad	bronchial
49	chr7:85225000-85225600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr7:85225000-85225600	Enhancers	Fetal Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links