Variant report

Variant	nsv817986
Chromosome Location	chr22:29540297-29568963
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:44)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

No data

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:29545744..29548830-chr22:29599572..29603786,4	K562	blood:
2	chr22:29560241..29562794-chr22:29564787..29567171,2	K562	blood:
3	chr22:29474405..29475082-chr22:29550138..29550829,2	MCF-7	breast:
4	chr22:29567775..29570590-chr22:29581265..29582805,2	MCF-7	breast:
5	chr22:29194152..29196570-chr22:29538750..29540833,2	MCF-7	breast:
6	chr22:29548200..29550640-chr22:29663832..29665499,3	K562	blood:
7	chr22:29507172..29508987-chr22:29549481..29552085,2	K562	blood:
8	chr22:29194920..29197276-chr22:29549664..29552289,2	MCF-7	breast:
9	chr22:29490386..29492445-chr22:29548625..29550170,2	K562	blood:
10	chr22:29452982..29455388-chr22:29548922..29550730,2	K562	blood:
11	chr22:29549443..29550329-chr22:29641671..29642180,2	MCF-7	breast:
12	chr22:29468687..29470195-chr22:29550149..29552502,2	K562	blood:
13	chr22:29507934..29508767-chr22:29550080..29551029,6	MCF-7	breast:
14	chr22:29468709..29469553-chr22:29550141..29550652,2	MCF-7	breast:
15	chr22:29477953..29480319-chr22:29546529..29549187,2	K562	blood:
16	chr22:29458794..29462861-chr22:29545928..29550252,4	K562	blood:
17	chr22:29540159..29541896-chr22:29549831..29552578,2	MCF-7	breast:
18	chr22:29468223..29470977-chr22:29546508..29548463,2	K562	blood:
19	chr22:29547025..29550393-chr22:29551126..29554117,6	K562	blood:
20	chr22:29442673..29444678-chr22:29547602..29550105,2	K562	blood:
21	chr22:29547323..29550128-chr22:29627116..29629585,2	K562	blood:
22	chr22:29277969..29280720-chr22:29548562..29550591,2	K562	blood:
23	chr22:29544270..29547165-chr22:29570652..29572572,2	K562	blood:
24	chr22:29464232..29466392-chr22:29545552..29548185,2	K562	blood:
25	chr22:29560241..29562794-chr22:29564787..29567171,2	K562	blood:
26	chr22:29540159..29541896-chr22:29549831..29552578,2	MCF-7	breast:
27	chr22:29548237..29550039-chr22:29662388..29664914,2	K562	blood:
28	chr22:29552955..29555263-chr22:29600441..29601965,2	K562	blood:
29	chr22:29547186..29550540-chr22:29600434..29604790,4	K562	blood:
30	chr22:29552265..29553268-chr22:29641211..29642160,5	MCF-7	breast:
31	chr22:29428793..29430315-chr22:29546051..29548231,2	K562	blood:
32	chr22:29547025..29550393-chr22:29551126..29554117,6	K562	blood:
33	chr22:29508205..29511663-chr22:29545622..29548558,3	K562	blood:
34	chr22:29550189..29551060-chr22:29641253..29641991,3	MCF-7	breast:
35	chr22:29555706..29558630-chr22:29601118..29603816,2	K562	blood:
36	chr22:29448833..29450694-chr22:29548349..29551156,2	K562	blood:
37	chr22:29478819..29480764-chr22:29547002..29549187,2	K562	blood:
38	chr22:29277682..29280421-chr22:29547829..29550165,4	K562	blood:
39	chr22:29476336..29477171-chr22:29550139..29551099,3	MCF-7	breast:
40	chr22:29568099..29570164-chr22:29580490..29582508,2	K562	blood:
41	chr22:29472899..29476008-chr22:29545567..29548841,3	K562	blood:
42	chr22:29468094..29470256-chr22:29547375..29550121,2	K562	blood:
43	chr22:29488253..29490159-chr22:29547499..29549684,2	K562	blood:
44	chr22:29444708..29447348-chr22:29547700..29550186,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EMID1-4	chr22:29550326-29550757	NONHSAT084673

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KREMEN1	hsa-miR-30c-5p	chr22:29542202-29542208
2	KREMEN1	hsa-miR-149-5p	chr22:29564090-29564115

Variant related genes	Relation type
ENSG00000186998	chromatin interactions
ENSG00000226471	chromatin interactions
ENSG00000100263	chromatin interactions
ENSG00000100219	chromatin interactions
ENSG00000182944	chromatin interactions
ENSG00000226772	chromatin interactions
ENSG00000183579	chromatin interactions
ENSG00000183762	chromatin interactions

Extended variants
information (count: 1196 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1196 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6006029	chr22:29540297-29540298	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552351982	chr22:29540303-29540304	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs570634758	chr22:29540346-29540347	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565433044	chr22:29540349-29540350	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs59762117	chr22:29540366-29540367	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs149693993	chr22:29540453-29540454	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs8141093	chr22:29540456-29540457	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs114710335	chr22:29540491-29540492	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142508839	chr22:29540517-29540518	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs574948309	chr22:29540524-29540525	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545504528	chr22:29540550-29540551	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs549353374	chr22:29540570-29540571	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs558695160	chr22:29540573-29540574	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs114127861	chr22:29540582-29540583	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs16987164	chr22:29540588-29540589	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs376883591	chr22:29540638-29540639	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs371534321	chr22:29540647-29540648	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs5763004	chr22:29540649-29540650	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545465916	chr22:29540703-29540704	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530029817	chr22:29540704-29540705	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs144475295	chr22:29540708-29540709	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs563674110	chr22:29540731-29540732	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs17451302	chr22:29540742-29540743	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs552428396	chr22:29540744-29540745	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs114199238	chr22:29540759-29540760	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs373563943	chr22:29540760-29540761	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528316511	chr22:29540900-29540901	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs546569263	chr22:29540917-29540918	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs132280	chr22:29540920-29540921	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs142508263	chr22:29540929-29540930	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs151123228	chr22:29540954-29540955	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs183097548	chr22:29540960-29540961	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs539121825	chr22:29540984-29540985	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs115384160	chr22:29541043-29541044	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs577353298	chr22:29541074-29541075	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs111677053	chr22:29541105-29541106	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs553385852	chr22:29541106-29541107	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs16987166	chr22:29541134-29541135	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs542546244	chr22:29541143-29541144	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs547985188	chr22:29541239-29541240	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs563639866	chr22:29541256-29541257	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs530950330	chr22:29541268-29541269	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs186616475	chr22:29541298-29541299	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs564637975	chr22:29541361-29541362	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs78293984	chr22:29541378-29541379	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs546729127	chr22:29541396-29541397	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs527606493	chr22:29541425-29541426	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs5844838	chr22:29541426-29541427	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs568170848	chr22:29541429-29541430	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs529118647	chr22:29541441-29541442	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Cat eye syndrome	16708226	CNVD
Olfactory neuroblastoma	18408657	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:762 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29483400-29550200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr22:29517200-29546200	Strong transcription	Dnd41	blood
3	chr22:29522400-29541600	Weak transcription	HMEC	breast
4	chr22:29523400-29548200	Weak transcription	Stomach Mucosa	stomach
5	chr22:29525800-29544400	Weak transcription	NHLF	lung
6	chr22:29526200-29542800	Weak transcription	Fetal Heart	heart
7	chr22:29526200-29547000	Weak transcription	K562	blood
8	chr22:29527600-29548000	Strong transcription	Fetal Intestine Small	intestine
9	chr22:29528600-29544400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr22:29529400-29547000	Strong transcription	Thymus	Thymus
11	chr22:29530000-29541400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr22:29530800-29546800	Genic enhancers	Fetal Muscle Leg	muscle
13	chr22:29531000-29540800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr22:29531000-29541000	Strong transcription	Stomach Smooth Muscle	stomach
15	chr22:29531600-29542800	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr22:29531600-29548400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr22:29533000-29543200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr22:29533000-29545600	Strong transcription	Fetal Intestine Large	intestine
19	chr22:29533200-29543200	Strong transcription	Fetal Stomach	stomach
20	chr22:29533600-29542400	Strong transcription	Duodenum Mucosa	Duodenum
21	chr22:29533800-29543600	Strong transcription	Fetal Brain Female	brain
22	chr22:29534600-29540600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr22:29534800-29540400	Weak transcription	Gastric	stomach
24	chr22:29534800-29545600	Weak transcription	Aorta	Aorta
25	chr22:29535400-29540600	Weak transcription	NHEK	skin
26	chr22:29536000-29541000	Strong transcription	Placenta Amnion	Placenta Amnion
27	chr22:29536400-29542400	Weak transcription	Brain Substantia Nigra	brain
28	chr22:29536400-29543000	Weak transcription	Brain Angular Gyrus	brain
29	chr22:29536600-29543000	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr22:29536600-29548200	Weak transcription	Fetal Kidney	kidney
31	chr22:29536800-29540400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr22:29536800-29540400	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr22:29536800-29541200	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr22:29537000-29541800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr22:29537000-29543600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr22:29537200-29542000	Strong transcription	Right Ventricle	heart
37	chr22:29537200-29543600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr22:29537200-29548200	Weak transcription	Fetal Brain Male	brain
39	chr22:29537400-29541800	Weak transcription	HepG2	liver
40	chr22:29537400-29545800	Genic enhancers	Fetal Muscle Trunk	muscle
41	chr22:29537600-29540600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr22:29537800-29541200	Strong transcription	Brain Hippocampus Middle	brain
43	chr22:29538000-29543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr22:29538200-29541800	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr22:29538200-29542000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr22:29538200-29543000	Weak transcription	Brain Cingulate Gyrus	brain
47	chr22:29538200-29545600	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr22:29538400-29544400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr22:29538400-29547400	Weak transcription	Pancreas	Pancrea
50	chr22:29538400-29548200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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