Variant report

Variant	nsv564656
Chromosome Location	chr14:44445118-44634641
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	ARID3A	chr14:44479441-44480344	HepG2	liver:	n/a	n/a
2	BACH1	chr14:44632100-44632238	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr14:44618833-44619126	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr14:44633192-44633496	Hela-S3	cervix:	n/a	chr14:44633351-44633362
5	CEBPB	chr14:44595859-44595978	A549	lung:	n/a	n/a
6	CEBPB	chr14:44582232-44582510	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr14:44606767-44606976	H1-hESC	embryonic stem cell:	n/a	chr14:44606862-44606873
8	CEBPB	chr14:44478922-44479645	HepG2	liver:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
9	CEBPB	chr14:44479333-44479685	ECC-1	luminal epithelium:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
10	CEBPB	chr14:44478929-44479169	A549	lung:	n/a	n/a
11	CEBPB	chr14:44499135-44499425	MCF-7	breast:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44499340-44499351
12	CEBPB	chr14:44560911-44561241	HepG2	liver:	n/a	chr14:44561060-44561071
13	CEBPB	chr14:44484998-44485226	HepG2	liver:	n/a	chr14:44485063-44485074
14	CEBPB	chr14:44479378-44479560	HepG2	liver:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
15	CEBPB	chr14:44452992-44453227	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr14:44572581-44572713	HepG2	liver:	n/a	chr14:44572646-44572657 chr14:44572645-44572658
17	CEBPB	chr14:44606738-44606986	HepG2	liver:	n/a	chr14:44606862-44606873
18	CEBPB	chr14:44479371-44479562	MCF-7	breast:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
19	CEBPB	chr14:44560981-44561240	A549	lung:	n/a	chr14:44561060-44561071
20	CEBPB	chr14:44605865-44606139	A549	lung:	n/a	chr14:44605990-44606001 chr14:44605988-44606001 chr14:44605988-44605999 chr14:44605990-44606001
21	CEBPB	chr14:44479304-44479659	ECC-1	luminal epithelium:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
22	CEBPB	chr14:44605796-44606154	Hela-S3	cervix:	n/a	chr14:44605990-44606001 chr14:44605988-44606001 chr14:44605988-44605999 chr14:44605990-44606001
23	CEBPB	chr14:44541354-44541571	HepG2	liver:	n/a	chr14:44541425-44541436
24	CEBPB	chr14:44487307-44487471	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:44599875-44600120	HepG2	liver:	n/a	chr14:44599949-44599960
26	CEBPB	chr14:44498838-44499445	A549	lung:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44498983-44498994 chr14:44499340-44499351
27	CEBPB	chr14:44499069-44499521	Hela-S3	cervix:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44499340-44499351
28	CEBPB	chr14:44605817-44606143	HepG2	liver:	n/a	chr14:44605990-44606001 chr14:44605988-44606001 chr14:44605988-44605999 chr14:44605990-44606001
29	CEBPB	chr14:44633186-44633505	HepG2	liver:	n/a	chr14:44633351-44633362
30	CEBPB	chr14:44498807-44499464	HepG2	liver:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44498983-44498994 chr14:44499340-44499351
31	CEBPB	chr14:44560924-44561243	H1-hESC	embryonic stem cell:	n/a	chr14:44561060-44561071
32	CEBPB	chr14:44560929-44561184	K562	blood:	n/a	chr14:44561060-44561071
33	CEBPB	chr14:44560911-44561219	IMR90	lung:	n/a	chr14:44561060-44561071
34	CEBPB	chr14:44599593-44600126	A549	lung:	n/a	chr14:44599949-44599960
35	CEBPB	chr14:44487331-44487496	A549	lung:	n/a	n/a
36	CEBPB	chr14:44450644-44451128	HepG2	liver:	n/a	n/a
37	CEBPB	chr14:44498824-44499447	IMR90	lung:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44498983-44498994 chr14:44499340-44499351
38	CEBPB	chr14:44595881-44596093	HepG2	liver:	n/a	n/a
39	CEBPB	chr14:44618834-44619117	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr14:44448312-44448448	HepG2	liver:	n/a	chr14:44448367-44448378
41	CEBPB	chr14:44499216-44499416	H1-hESC	embryonic stem cell:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44499340-44499351
42	CEBPB	chr14:44478922-44479578	IMR90	lung:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
43	CHD2	chr14:44618838-44619102	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr14:44618860-44619010	NHEK	skin:	n/a	chr14:44618936-44618957 chr14:44618941-44618959 chr14:44618942-44618958
45	CTCF	chr14:44618880-44619030	HBMEC	blood vessel:	n/a	chr14:44618936-44618957 chr14:44618941-44618959 chr14:44618942-44618958
46	CTCF	chr14:44618925-44619039	GM13976	blood:	n/a	chr14:44618936-44618957 chr14:44618941-44618959 chr14:44618942-44618958
47	CTCF	chr14:44618780-44618930	BE2_C	brain:	n/a	n/a
48	CTCF	chr14:44631579-44631629	MCF-7	breast:	n/a	n/a
49	CTCF	chr14:44618840-44618990	GM12875	blood:	n/a	chr14:44618936-44618957 chr14:44618941-44618959 chr14:44618942-44618958
50	CTCF	chr14:44618860-44619010	GM12874	blood:	n/a	chr14:44618936-44618957 chr14:44618941-44618959 chr14:44618942-44618958

No.	Distal block	Cell Line	Cell type
1	chr14:44600217..44602036-chr14:44604194..44606588,2	K562	blood:
2	chr14:44606810..44610792-chr14:44612494..44615788,3	K562	blood:
3	chr14:44370633..44373508-chr14:44616084..44618482,2	MCF-7	breast:
4	chr14:44562970..44563903-chr14:44618440..44619350,3	MCF-7	breast:
5	chr14:44480170..44481920-chr14:44484152..44486382,2	MCF-7	breast:
6	chr14:44606810..44610792-chr14:44612494..44615788,3	K562	blood:
7	chr14:44480170..44481920-chr14:44484152..44486382,2	MCF-7	breast:
8	chr14:44569949..44570449-chr8:101630587..101631141,2	MCF-7	breast:
9	chr14:44562970..44563903-chr14:44618440..44619350,3	MCF-7	breast:
10	chr14:44600217..44602036-chr14:44604194..44606588,2	K562	blood:
11	chr14:44370246..44372256-chr14:44617257..44619025,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-6	chr14:44621821-44621918	l_977_chr14:44621312-44622966_testes
2	lnc-FSCB-6	chr14:44622425-44622966	l_977_chr14:44621312-44622966_testes
3	lnc-FSCB-6	chr14:44621313-44621629	l_977_chr14:44621312-44622966_testes
4	lnc-FSCB-2	chr14:44464984-44465046	ENSG00000258969
5	lnc-FSCB-8	chr14:44477505-44479523	ucscGeneNc_uc001wvs_1
6	lnc-FSCB-7	chr14:44546737-44547087	NONHSAT036603
7	lnc-FSCB-2	chr14:44518586-44518710	ENSG00000258969
8	lnc-FSCB-6	chr14:44622029-44622354	l_977_chr14:44621312-44622966_testes

Variant related genes	Relation type
ENSG00000259137	TF binding region
ENSG00000259019	TF binding region
ENSG00000174226	chromatin interactions
ENSG00000253740	chromatin interactions

Extended variants
information (count: 1527 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1527 , 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	rs112482777	chr14:44447815-44447816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183351162	chr14:44447874-44447875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544789174	chr14:44447910-44447911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188813715	chr14:44447921-44447922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs941944	chr14:44447955-44447956	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs370540110	chr14:44448067-44448068	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs374176455	chr14:44448068-44448069	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs33953097	chr14:44448069-44448070	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs3035452	chr14:44448071-44448072	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs374568920	chr14:44448072-44448073	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs368575282	chr14:44448073-44448074	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs112211347	chr14:44448076-44448077	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs8020694	chr14:44448083-44448084	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs560788552	chr14:44448085-44448086	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs150600221	chr14:44448104-44448105	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs10150907	chr14:44448110-44448111	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs374442475	chr14:44448158-44448159	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs552957451	chr14:44448200-44448201	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs564158920	chr14:44448255-44448256	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs114755468	chr14:44448318-44448319	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs549552789	chr14:44448352-44448353	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs191764464	chr14:44448377-44448378	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs368054899	chr14:44448424-44448425	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs116577742	chr14:44448438-44448439	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs373745690	chr14:44448457-44448458	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs547255542	chr14:44448476-44448477	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs560789457	chr14:44448480-44448481	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs565649149	chr14:44448525-44448526	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs11629112	chr14:44448569-44448570	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs184010340	chr14:44448577-44448578	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs577258715	chr14:44448603-44448604	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs561027498	chr14:44448612-44448613	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs143410935	chr14:44448645-44448646	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs4900652	chr14:44448646-44448647	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs569957253	chr14:44448670-44448671	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs375300562	chr14:44448714-44448715	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs544521218	chr14:44448790-44448791	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs542456398	chr14:44448856-44448857	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs77564853	chr14:44448870-44448871	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs79138282	chr14:44448874-44448875	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs564616605	chr14:44448892-44448893	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs557018356	chr14:44448920-44448921	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs545777744	chr14:44448929-44448930	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs563962570	chr14:44448959-44448960	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs188749788	chr14:44448963-44448964	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs191325366	chr14:44448964-44448965	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs183895593	chr14:44448965-44448966	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs529014798	chr14:44448975-44448976	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs547194031	chr14:44448984-44448985	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs386776965	chr14:44449014-44449015	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44447800-44448000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:44448000-44449800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr14:44450400-44450800	Enhancers	Fetal Intestine Small	intestine
4	chr14:44450400-44451200	Enhancers	Liver	Liver
5	chr14:44450400-44451200	Enhancers	Fetal Intestine Large	intestine
6	chr14:44450600-44451200	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr14:44450600-44451200	Enhancers	HepG2	liver
8	chr14:44450800-44451400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr14:44464800-44465000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr14:44472800-44473000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr14:44473600-44473800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:44478400-44481000	Enhancers	Liver	Liver
13	chr14:44479000-44480800	Enhancers	HepG2	liver
14	chr14:44496600-44497000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr14:44497000-44498800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr14:44497600-44497800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr14:44498800-44499800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr14:44498800-44500600	Enhancers	Fetal Intestine Large	intestine
19	chr14:44499600-44500000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr14:44499600-44500200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr14:44499600-44500400	Enhancers	H9 Cell Line	embryonic stem cell
22	chr14:44499600-44500800	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr14:44499800-44500600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr14:44499800-44500600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr14:44499800-44500600	Enhancers	Fetal Intestine Small	intestine
26	chr14:44499800-44501000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr14:44500000-44500200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr14:44500000-44500400	Enhancers	H1 Cell Line	embryonic stem cell
29	chr14:44500000-44500400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr14:44500000-44500400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr14:44500000-44500400	Enhancers	Fetal Heart	heart
32	chr14:44500000-44500600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr14:44500000-44500600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr14:44500000-44500600	Enhancers	Fetal Stomach	stomach
35	chr14:44500000-44500800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr14:44500000-44500800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr14:44500000-44501000	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr14:44500000-44501000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr14:44500200-44500600	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr14:44500200-44500800	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr14:44500200-44500800	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr14:44500200-44501400	Enhancers	Brain Germinal Matrix	brain
43	chr14:44500400-44500600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr14:44500600-44500800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr14:44507600-44509200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr14:44508400-44508600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:44508600-44509200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr14:44510000-44510200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr14:44514000-44514400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr14:44526000-44526200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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