Variant report

Variant	nsv529910
Chromosome Location	chrX:65738026-66025016
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1445)
CpG islands
(count:306)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1445 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:65951290-65951590	K562	blood:	n/a	n/a
2	ARID3A	chrX:65948594-65949132	K562	blood:	n/a	n/a
3	ARID3A	chrX:65951349-65951572	HepG2	liver:	n/a	n/a
4	ATF1	chrX:65948586-65949187	K562	blood:	n/a	n/a
5	ATF2	chrX:65845358-65845783	GM12878	blood:	n/a	n/a
6	BATF	chrX:65858992-65859189	GM12878	blood:	n/a	chrX:65859077-65859087 chrX:65859076-65859087
7	BHLHE40	chrX:65963483-65963487	GM12878	blood:	n/a	n/a
8	BHLHE40	chrX:65977939-65978034	GM12878	blood:	n/a	n/a
9	BHLHE40	chrX:65949014-65949167	GM12878	blood:	n/a	n/a
10	BHLHE40	chrX:65858137-65858650	HepG2	liver:	n/a	n/a
11	BHLHE40	chrX:65951357-65951550	GM12878	blood:	n/a	n/a
12	BHLHE40	chrX:65948789-65949213	K562	blood:	n/a	n/a
13	BHLHE40	chrX:65858290-65858746	GM12878	blood:	n/a	n/a
14	BRCA1	chrX:65948601-65949144	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chrX:65948612-65949157	K562	blood:	n/a	n/a
16	CEBPB	chrX:65842271-65842542	IMR90	lung:	n/a	n/a
17	CEBPB	chrX:65905478-65905769	HepG2	liver:	n/a	chrX:65905636-65905647
18	CEBPB	chrX:65964333-65964533	IMR90	lung:	n/a	n/a
19	CEBPB	chrX:65743827-65743964	A549	lung:	n/a	n/a
20	CEBPB	chrX:65858925-65859280	A549	lung:	n/a	n/a
21	CEBPB	chrX:65897430-65897735	IMR90	lung:	n/a	n/a
22	CEBPB	chrX:65808358-65808600	IMR90	lung:	n/a	n/a
23	CEBPB	chrX:65855213-65855580	IMR90	lung:	n/a	n/a
24	CEBPB	chrX:65896305-65897200	IMR90	lung:	n/a	n/a
25	CEBPB	chrX:65853337-65853731	IMR90	lung:	n/a	n/a
26	CEBPB	chrX:65948762-65949166	K562	blood:	n/a	n/a
27	CEBPB	chrX:65948901-65949187	IMR90	lung:	n/a	n/a
28	CEBPB	chrX:65905474-65905770	IMR90	lung:	n/a	chrX:65905636-65905647
29	CEBPB	chrX:65858749-65859261	HepG2	liver:	n/a	n/a
30	CEBPB	chrX:65744634-65744749	IMR90	lung:	n/a	n/a
31	CEBPB	chrX:65999479-65999694	IMR90	lung:	n/a	n/a
32	CEBPB	chrX:65808392-65808578	A549	lung:	n/a	n/a
33	CEBPB	chrX:65905548-65905744	K562	blood:	n/a	chrX:65905636-65905647
34	CEBPB	chrX:65824836-65825136	HepG2	liver:	n/a	chrX:65824967-65824978
35	CEBPB	chrX:65903973-65904229	HepG2	liver:	n/a	chrX:65904074-65904085 chrX:65904072-65904089
36	CEBPB	chrX:65858970-65859257	IMR90	lung:	n/a	n/a
37	CHD1	chrX:65858225-65858759	GM12878	blood:	n/a	n/a
38	CHD2	chrX:65859034-65859451	GM12878	blood:	n/a	n/a
39	CREB1	chrX:65948606-65949020	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chrX:65948620-65949204	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chrX:65948653-65949048	A549	lung:	n/a	n/a
42	CREB1	chrX:65948613-65949203	GM12878	blood:	n/a	n/a
43	CREB1	chrX:65948459-65949229	K562	blood:	n/a	n/a
44	CREB1	chrX:65948577-65949100	A549	lung:	n/a	n/a
45	CTCF	chrX:65959860-65959972	GM10266	blood:	n/a	n/a
46	CTCF	chrX:65951300-65951450	MCF-7	breast:	n/a	chrX:65951334-65951352 chrX:65951336-65951349
47	CTCF	chrX:66010219-66010250	LNCaP	prostate:	n/a	n/a
48	CTCF	chrX:65981462-65981530	GM10266	blood:	n/a	n/a
49	CTCF	chrX:65948624-65949278	MCF-7	breast:	n/a	chrX:65949022-65949038 chrX:65948720-65948741
50	CTCF	chrX:65903641-65903661	GM10266	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:65836683-65836733	K562	blood:	n/a
2	chrX:65836683-65836733	K562	blood:	n/a
3	chrX:65825449-65825499	Caco-2	colon:	n/a
4	chrX:65818628-65818678	ECC-1	luminal epithelium:	n/a
5	chrX:65818628-65818678	HUVEC	blood vessel:	n/a
6	chrX:65825449-65825499	MCF10A-Er-Src	breast:	n/a
7	chrX:65836683-65836733	PFSK-1	brain:	n/a
8	chrX:65836683-65836733	CMK	blood:	n/a
9	chrX:65818628-65818678	CMK	blood:	n/a
10	chrX:65835992-65836042	Hepatocyte	liver:	n/a
11	chrX:65835992-65836042	Caco-2	colon:	n/a
12	chrX:65825449-65825499	HNPCEpiC	eye:	n/a
13	chrX:65835992-65836042	HAEpiC	amniotic membrane:	n/a
14	chrX:65836683-65836733	Jurkat	blood:	n/a
15	chrX:65835804-65835854	NHBE	bronchial:	n/a
16	chrX:65836683-65836733	RPTEC	kidney:	n/a
17	chrX:65836683-65836733	HEEpiC	esophagus:	n/a
18	chrX:65825449-65825499	Hela-S3	cervix:	n/a
19	chrX:65835804-65835854	BE2_C	brain:	n/a
20	chrX:65818628-65818678	AoSMC	blood vessel:	n/a
21	chrX:65835992-65836042	A549	lung:	n/a
22	chrX:65835992-65836042	NB4	blood:	n/a
23	chrX:65835804-65835854	ECC-1	luminal epithelium:	n/a
24	chrX:65818628-65818678	BJ	skin:	n/a
25	chrX:65825449-65825499	GM06990	blood:	n/a
26	chrX:65835992-65836042	RPTEC	kidney:	n/a
27	chrX:65825449-65825499	ECC-1	luminal epithelium:	n/a
28	chrX:65825449-65825499	LNCaP	prostate:	n/a
29	chrX:65818628-65818678	AG10803	skin:	n/a
30	chrX:65835804-65835854	PFSK-1	brain:	n/a
31	chrX:65818628-65818678	MCF-7	breast:	n/a
32	chrX:65836683-65836733	ProgFib	skin:	n/a
33	chrX:65835804-65835854	GM12878	blood:	n/a
34	chrX:65835804-65835854	GM19239	blood:	n/a
35	chrX:65836683-65836733	HEK293	kidney:	embryo
36	chrX:65836683-65836733	NB4	blood:	n/a
37	chrX:65836683-65836733	T-47D	breast:	n/a
38	chrX:65835992-65836042	Hela-S3	cervix:	n/a
39	chrX:65818628-65818678	HCT-116	colon:	n/a
40	chrX:65825449-65825499	AG04450	lung:	fetal
41	chrX:65818628-65818678	NHDF-neo	bronchial:	n/a
42	chrX:65825449-65825499	Jurkat	blood:	n/a
43	chrX:65818628-65818678	HCPEpiC	choroid plexus:	n/a
44	chrX:65825449-65825499	HIPEpiC	eye:	n/a
45	chrX:65835992-65836042	SKMC	muscle:	n/a
46	chrX:65818628-65818678	NH-A	brain:	n/a
47	chrX:65835804-65835854	HUVEC	blood vessel:	n/a
48	chrX:65825449-65825499	HMEC	breast:	n/a
49	chrX:65835992-65836042	BE2_C	brain:	n/a
50	chrX:65825449-65825499	SK-N-SH_RA	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:65421200..65421901-chrX:65948234..65949098,4	MCF-7	breast:
2	chrX:65980206..65981190-chrX:67238110..67238888,2	MCF-7	breast:
3	chr5:102455761..102456262-chrX:66015381..66015881,2	Hela-S3	cervix:
4	chrX:65879551..65882090-chrX:65883298..65886042,2	K562	blood:
5	chrX:65852587..65855545-chrX:65857055..65858751,2	K562	blood:
6	chrX:65852587..65855545-chrX:65857055..65858751,2	K562	blood:
7	chr1:16839287..16842291-chrX:65944500..65946020,4	K562	blood:
8	chrX:65696857..65699812-chrX:65924534..65926662,2	MCF-7	breast:
9	chrX:64801614..64802539-chrX:65948756..65949257,2	MCF-7	breast:
10	chrX:65420975..65421894-chrX:65948233..65949029,2	MCF-7	breast:
11	chrX:65420456..65421112-chrX:65948321..65948834,2	MCF-7	breast:
12	chrX:65879551..65882090-chrX:65883298..65886042,2	K562	blood:
13	chrX:65330062..65330591-chrX:65948300..65949050,3	MCF-7	breast:
14	chr1:16838565..16842080-chrX:65944520..65947520,4	K562	blood:
15	chrX:65628289..65628799-chrX:65948303..65948910,3	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-394P	TF binding region
EDA2R	TF binding region
RNU6-394P	CpG island
EDA2R	CpG island
ENSG00000145725	chromatin interactions
ENSG00000261135	chromatin interactions
ENSG00000145723	chromatin interactions
ENSG00000206652	chromatin interactions

Extended variants
information (count: 1132 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:1132 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184017494	chrX:65773800-65773801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371596851	chrX:65773826-65773827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371799218	chrX:65773851-65773852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188799963	chrX:65773860-65773861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374967934	chrX:65773876-65773877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142238027	chrX:65773879-65773880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs56304615	chrX:65773966-65773967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs180775824	chrX:65774101-65774102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141264041	chrX:65774145-65774146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144987955	chrX:65774161-65774162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs28791506	chrX:65774276-65774277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374920731	chrX:65774310-65774311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185490358	chrX:65774321-65774322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140505167	chrX:65774377-65774378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189215296	chrX:65774402-65774403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150447714	chrX:65774408-65774409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs79968358	chrX:65774443-65774444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs5964547	chrX:65774461-65774462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1601452	chrX:65774588-65774589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370169646	chrX:65809826-65809827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191201154	chrX:65809905-65809906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73221522	chrX:65809967-65809968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373739782	chrX:65810064-65810065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs5919159	chrX:65810074-65810075	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs372747130	chrX:65810109-65810110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564721225	chrX:65810154-65810155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149270666	chrX:65810179-65810180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144470596	chrX:65810188-65810189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181958375	chrX:65810213-65810214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34554674	chrX:65810229-65810230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186788618	chrX:65810368-65810369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79168331	chrX:65810493-65810494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191664872	chrX:65810577-65810578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183123187	chrX:65810580-65810581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188110253	chrX:65810585-65810586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189620920	chrX:65810586-65810587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141717890	chrX:65810596-65810597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146005689	chrX:65810625-65810626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371064672	chrX:65810663-65810664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371095071	chrX:65810683-65810684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113674269	chrX:65810692-65810693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182349882	chrX:65810777-65810778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187728223	chrX:65810806-65810807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374585260	chrX:65810911-65810912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192335232	chrX:65810940-65810941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376371022	chrX:65811125-65811126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184780569	chrX:65811159-65811160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188525790	chrX:65811172-65811173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192973734	chrX:65811270-65811271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139959596	chrX:65811369-65811370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:48)

Disease	PMID	Source
Intellectual disability	23615299	CNVD
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Astrocytoma	17387387	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	22286061	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Astrocytoma	22246337	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Craniofrontonasal syndrome	21572526	CNVD
Cerebellar hypoplasia	21569638	CNVD
Disorders of sex development	21048976	CNVD
Myxofibrosarcoma	16751306	CNVD
Cervical cancer	21062161	CNVD
Cancer	22429812	CNVD
Cancer	16751803	CNVD
Prostate cancer	21147910	CNVD
Intellectual disability	22102821	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:761 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:65773800-65774600	Enhancers	Dnd41	blood
2	chrX:65809800-65812200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chrX:65810200-65827400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chrX:65811000-65812800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chrX:65811200-65812800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chrX:65811200-65812800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chrX:65811200-65816400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chrX:65811200-65817000	Weak transcription	HSMM	muscle
9	chrX:65811400-65819400	Weak transcription	HMEC	breast
10	chrX:65811600-65815400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chrX:65811600-65816200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chrX:65811800-65815000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chrX:65811800-65817000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chrX:65811800-65817200	Weak transcription	Ovary	ovary
15	chrX:65811800-65821000	Weak transcription	NHDF-Ad	bronchial
16	chrX:65812000-65815000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chrX:65812000-65816200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chrX:65812200-65813200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chrX:65812200-65813600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chrX:65812800-65813200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chrX:65812800-65813800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
22	chrX:65812800-65814000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chrX:65812800-65823400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chrX:65812800-65825600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chrX:65813000-65814000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
26	chrX:65813200-65813400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
27	chrX:65813200-65813400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
28	chrX:65813200-65813600	ZNF genes & repeats	NH-A	brain
29	chrX:65813200-65814000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chrX:65813200-65814000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chrX:65813400-65813800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
32	chrX:65813400-65816400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chrX:65813400-65817200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chrX:65813600-65817200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chrX:65813600-65817800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
36	chrX:65813600-65817800	Weak transcription	NH-A	brain
37	chrX:65813800-65814000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
38	chrX:65813800-65814200	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chrX:65813800-65814200	Strong transcription	Duodenum Smooth Muscle	Duodenum
40	chrX:65813800-65816200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chrX:65813800-65816200	Weak transcription	Aorta	Aorta
42	chrX:65813800-65817000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chrX:65814000-65815000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chrX:65814000-65816200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chrX:65814000-65816400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chrX:65814000-65816600	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chrX:65814000-65817000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chrX:65814200-65816600	Weak transcription	HSMMtube	muscle
49	chrX:65814200-65816800	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chrX:65814200-65816800	Weak transcription	A549	lung

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