Variant report

Variant	nsv1034520
Chromosome Location	chr6:62967960-63057406
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	ATF2	chr6:63008621-63009133	GM12878	blood:	n/a	n/a
2	ATF2	chr6:63008561-63009076	GM12878	blood:	n/a	n/a
3	BACH1	chr6:62995853-62996194	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:62996403-62996585	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:63036580-63036810	H1-hESC	embryonic stem cell:	n/a	chr6:63036749-63036763
6	BCL11A	chr6:63008564-63009026	GM12878	blood:	n/a	n/a
7	BCL3	chr6:63008674-63008913	GM12878	blood:	n/a	n/a
8	BCLAF1	chr6:63008581-63009054	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:63008716-63009043	GM12878	blood:	n/a	n/a
10	CEBPB	chr6:62993180-62993341	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr6:63001581-63001758	IMR90	lung:	n/a	n/a
12	CEBPB	chr6:62990637-62990985	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr6:63007518-63007799	HepG2	liver:	n/a	chr6:63007660-63007671
14	CEBPB	chr6:63007513-63007781	H1-hESC	embryonic stem cell:	n/a	chr6:63007660-63007671
15	CHD1	chr6:62996405-62996592	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr6:62995291-62995678	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr6:62995987-62996395	GM12878	blood:	n/a	n/a
18	CHD2	chr6:63008709-63008997	GM12878	blood:	n/a	n/a
19	CHD2	chr6:62996138-62996202	HepG2	liver:	n/a	n/a
20	CHD2	chr6:62995869-62996419	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr6:62996632-62996646	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr6:62983654-62983696	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr6:63008643-63009121	GM12878	blood:	n/a	n/a
24	CTBP2	chr6:62995575-62996700	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr6:62993820-62993970	GM12865	blood:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
26	CTCF	chr6:62993820-62993970	HPF	lung:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
27	CTCF	chr6:62993820-62993970	SK-N-SH_RA	brain:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
28	CTCF	chr6:62993680-62993830	NHEK	skin:	n/a	n/a
29	CTCF	chr6:62993880-62994030	GM12872	blood:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
30	CTCF	chr6:62999057-62999105	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr6:62993840-62993990	AG09309	skin:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
32	CTCF	chr6:62993020-62993170	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr6:62993900-62994050	GM12873	blood:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
34	CTCF	chr6:62993840-62993990	MCF-7	breast:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
35	CTCF	chr6:62993820-62993970	NHEK	skin:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
36	CTCF	chr6:62993860-62994010	GM12873	blood:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
37	CTCF	chr6:62993820-62993970	GM12878	blood:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
38	CTCF	chr6:62993840-62993990	AG10803	skin:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
39	CTCF	chr6:62993900-62994050	HCT-116	colon:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
40	CTCF	chr6:62993832-62994017	Kidney_OC	kidney:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
41	CTCF	chr6:62995340-62995570	GM12872	blood:	n/a	n/a
42	CTCF	chr6:62993860-62994010	GM06990	blood:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
43	CTCF	chr6:62993860-62994010	GM12874	blood:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
44	CTCF	chr6:62993720-62993870	HAc	cerebellar:	n/a	n/a
45	CTCF	chr6:62993900-62994050	HFF	foreskin:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
46	CTCF	chr6:62993899-62994012	MCF-7	breast:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
47	CTCF	chr6:62993801-62994037	LNCaP	prostate:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
48	CTCF	chr6:63055620-63055770	HEK293	kidney:	n/a	n/a
49	CTCF	chr6:62993856-62994001	HepG2	liver:	n/a	chr6:62993913-62993931 chr6:62993919-62993928
50	CTCF	chr6:62993860-62994010	AoAF	blood vessel:	n/a	chr6:62993913-62993931 chr6:62993919-62993928

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:63038652-63038702	RPTEC	kidney:	n/a
2	chr6:62995523-62995573	NHDF-neo	bronchial:	n/a
3	chr6:63038652-63038702	RPTEC	kidney:	n/a
4	chr6:62995523-62995573	NHDF-neo	bronchial:	n/a
5	chr6:62995963-62996013	IMR90	lung:	fetal
6	chr6:62996664-62996714	HUVEC	blood vessel:	n/a
7	chr6:62976042-62976092	ProgFib	skin:	n/a
8	chr6:62996627-62996677	GM12891	blood:	n/a
9	chr6:62995963-62996013	ovcar-3	ovarian:	n/a
10	chr6:62995523-62995573	HRPEpiC	eye:	n/a
11	chr6:62996664-62996714	HRPEpiC	eye:	n/a
12	chr6:62995963-62996013	HL-60	blood:	n/a
13	chr6:62996130-62996180	A549	lung:	n/a
14	chr6:62976042-62976092	SK-N-SH	brain:	n/a
15	chr6:62996132-62996182	GM12892	blood:	n/a
16	chr6:62996299-62996349	Jurkat	blood:	n/a
17	chr6:62996702-62996752	CMK	blood:	n/a
18	chr6:62996697-62996747	HRE	kidney:	n/a
19	chr6:62995523-62995573	IMR90	lung:	fetal
20	chr6:62976042-62976092	NB4	blood:	n/a
21	chr6:62996697-62996747	RPTEC	kidney:	n/a
22	chr6:62996130-62996180	AG04449	skin:	fetal
23	chr6:62996214-62996264	HUVEC	blood vessel:	n/a
24	chr6:62996214-62996264	NHDF-neo	bronchial:	n/a
25	chr6:62996183-62996233	SK-N-SH	brain:	n/a
26	chr6:62995876-62995926	BE2_C	brain:	n/a
27	chr6:62996697-62996747	AoSMC	blood vessel:	n/a
28	chr6:62995523-62995573	NB4	blood:	n/a
29	chr6:62996130-62996180	GM12892	blood:	n/a
30	chr6:62976042-62976092	HIPEpiC	eye:	n/a
31	chr6:62996022-62996072	AG04450	lung:	fetal
32	chr6:62996697-62996747	Jurkat	blood:	n/a
33	chr6:62996627-62996677	Hepatocyte	liver:	n/a
34	chr6:62976042-62976092	A549	lung:	n/a
35	chr6:62995876-62995926	AoSMC	blood vessel:	n/a
36	chr6:62996214-62996264	HPAEpiC	pulmonary alveolar:	n/a
37	chr6:62996702-62996752	HEEpiC	esophagus:	n/a
38	chr6:62976042-62976092	HL-60	blood:	n/a
39	chr6:62996183-62996233	GM19239	blood:	n/a
40	chr6:62976042-62976092	PANC-1	pancreas:	n/a
41	chr6:62976042-62976092	AG10803	skin:	n/a
42	chr6:62996702-62996752	NHBE	bronchial:	n/a
43	chr6:62996627-62996677	SK-N-SH_RA	brain:	n/a
44	chr6:62996130-62996180	NHDF-neo	bronchial:	n/a
45	chr6:62996664-62996714	AG04449	skin:	fetal
46	chr6:62996119-62996169	HEEpiC	esophagus:	n/a
47	chr6:62996697-62996747	PANC-1	pancreas:	n/a
48	chr6:62996022-62996072	AG09309	skin:	n/a
49	chr6:62996697-62996747	SK-N-SH	brain:	n/a
50	chr6:62996702-62996752	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:62973850..62974714-chr7:113350282..113350966,2	MCF-7	breast:
2	chr6:62518763..62519292-chr6:62993656..62994388,2	MCF-7	breast:

Variant related genes	Relation type
KHDRBS2	TF binding region
KHDRBS2	CpG island

Extended variants
information (count: 1539 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1539 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs855409	chr6:62967960-62967961	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541022426	chr6:62967998-62967999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539251191	chr6:62968018-62968019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138550339	chr6:62968034-62968035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559360095	chr6:62968072-62968073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144088100	chr6:62968082-62968083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147258754	chr6:62968115-62968116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553361634	chr6:62968120-62968121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574763187	chr6:62968129-62968130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545072728	chr6:62968164-62968165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140693467	chr6:62968173-62968174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563820961	chr6:62968202-62968203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115595034	chr6:62968222-62968223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546470276	chr6:62968242-62968243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183396680	chr6:62968243-62968244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112895797	chr6:62968291-62968292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs855410	chr6:62968296-62968297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187362014	chr6:62968307-62968308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536702241	chr6:62968348-62968349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562370777	chr6:62968376-62968377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377448590	chr6:62968383-62968384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368731577	chr6:62968424-62968425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139292638	chr6:62968430-62968431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530996090	chr6:62968498-62968499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556651854	chr6:62968512-62968513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs115102445	chr6:62968559-62968560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9346272	chr6:62968587-62968588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568657344	chr6:62968609-62968610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149932178	chr6:62968621-62968622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551586048	chr6:62968666-62968667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566528017	chr6:62968669-62968670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567055561	chr6:62968673-62968674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34278226	chr6:62968689-62968690	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs146474397	chr6:62968744-62968745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567511913	chr6:62968753-62968754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535855199	chr6:62968765-62968766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375372863	chr6:62968820-62968821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73488971	chr6:62968843-62968844	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs546306751	chr6:62968866-62968867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558202361	chr6:62968874-62968875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139992268	chr6:62968947-62968948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143481703	chr6:62968963-62968964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562244264	chr6:62968964-62968965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529540826	chr6:62968988-62968989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543844724	chr6:62969018-62969019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562127129	chr6:62969081-62969082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138554612	chr6:62969163-62969164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377021379	chr6:62969164-62969165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114788745	chr6:62969182-62969183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551210615	chr6:62969197-62969198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	CNVD
Lung cancer	19547694	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic cancer	17952125	CNVD
Autism	19492091	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:62944000-62988200	Weak transcription	Primary B cells from cord blood	blood
2	chr6:62969800-62970200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:62970400-62970800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:62974200-62974600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:62974600-62975000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:62974600-62975000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:62975000-62976400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:62975800-62976200	Enhancers	Fetal Intestine Small	intestine
9	chr6:62975800-62976400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:62976000-62977200	Enhancers	Primary B cells from peripheral blood	blood
11	chr6:62976400-62994400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:62988200-62988400	Enhancers	Primary B cells from peripheral blood	blood
13	chr6:62988200-62988800	Enhancers	Primary B cells from cord blood	blood
14	chr6:62988400-62989800	Weak transcription	Primary B cells from peripheral blood	blood
15	chr6:62988800-62993200	Weak transcription	Primary B cells from cord blood	blood
16	chr6:62989600-62990000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr6:62989600-62990000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr6:62989600-62990400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr6:62989800-62990400	Enhancers	Primary B cells from peripheral blood	blood
20	chr6:62990000-62991800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:62990000-62993600	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr6:62990400-62993400	Weak transcription	Primary B cells from peripheral blood	blood
23	chr6:62990400-62994000	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr6:62990800-62991000	Enhancers	Fetal Brain Female	brain
25	chr6:62991200-62992400	Weak transcription	Fetal Brain Female	brain
26	chr6:62991800-62996800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:62992400-62992600	Enhancers	Fetal Brain Female	brain
28	chr6:62992600-62993000	Enhancers	Fetal Intestine Small	intestine
29	chr6:62992600-62993200	Enhancers	Fetal Intestine Large	intestine
30	chr6:62992600-62994800	Active TSS	Fetal Brain Female	brain
31	chr6:62992600-62997000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
32	chr6:62992800-62994800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:62992800-62997000	Active TSS	Brain Angular Gyrus	brain
34	chr6:62992800-62997000	Active TSS	Brain Inferior Temporal Lobe	brain
35	chr6:62993000-62993200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr6:62993000-62993200	Active TSS	Fetal Intestine Small	intestine
37	chr6:62993000-62993400	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr6:62993000-62997000	Active TSS	Fetal Brain Male	brain
39	chr6:62993200-62993400	Flanking Active TSS	Fetal Intestine Large	intestine
40	chr6:62993200-62993400	Flanking Active TSS	Fetal Intestine Small	intestine
41	chr6:62993200-62993600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:62993200-62993600	Enhancers	Primary B cells from cord blood	blood
43	chr6:62993200-62993600	Active TSS	Fetal Kidney	kidney
44	chr6:62993200-62993800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr6:62993200-62993800	Active TSS	Brain Anterior Caudate	brain
46	chr6:62993200-62993800	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr6:62993200-62994000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr6:62993200-62996600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr6:62993400-62993600	Active TSS	Fetal Intestine Large	intestine
50	chr6:62993400-62993800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell

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