Variant report

Variant	nsv1037743
Chromosome Location	chr11:100498709-100521043
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:185)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:185 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:100509757-100509773	K562	blood:	n/a	n/a
2	BACH1	chr11:100505977-100506301	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr11:100506022-100506241	K562	blood:	n/a	n/a
4	BHLHE40	chr11:100509795-100510074	K562	blood:	n/a	n/a
5	CBX3	chr11:100519781-100519995	K562	blood:	n/a	n/a
6	CBX3	chr11:100520197-100520454	K562	blood:	n/a	n/a
7	CEBPB	chr11:100509587-100509605	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr11:100511990-100512287	IMR90	lung:	n/a	n/a
9	CEBPB	chr11:100509386-100509645	HepG2	liver:	n/a	chr11:100509515-100509528 chr11:100509516-100509527 chr11:100509515-100509526
10	CEBPB	chr11:100509372-100509687	K562	blood:	n/a	chr11:100509515-100509528 chr11:100509516-100509527 chr11:100509515-100509526
11	CEBPB	chr11:100509360-100510055	IMR90	lung:	n/a	chr11:100509515-100509528 chr11:100509516-100509527 chr11:100509515-100509526
12	CEBPB	chr11:100518562-100518621	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr11:100505606-100505878	K562	blood:	n/a	n/a
14	CHD2	chr11:100518789-100518862	K562	blood:	n/a	n/a
15	CTCF	chr11:100500411-100500737	K562	blood:	n/a	n/a
16	CTCF	chr11:100510540-100510690	AG04450	lung:	n/a	n/a
17	CTCF	chr11:100500572-100500612	MCF-7	breast:	n/a	n/a
18	CTCF	chr11:100500480-100500630	GM06990	blood:	n/a	n/a
19	CTCF	chr11:100500500-100500650	HA-sp	spinal cord:	n/a	n/a
20	CTCF	chr11:100500400-100500550	GM12872	blood:	n/a	n/a
21	CTCF	chr11:100500520-100500670	MCF-7	breast:	n/a	n/a
22	CTCF	chr11:100500512-100500647	GM19239	blood:	n/a	n/a
23	CTCF	chr11:100500460-100500610	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr11:100500420-100500570	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr11:100502240-100502390	BE2_C	brain:	n/a	chr11:100502243-100502251
26	CTCF	chr11:100500467-100500664	MCF-7	breast:	n/a	n/a
27	CTCF	chr11:100500394-100500731	GM12878	blood:	n/a	n/a
28	CTCF	chr11:100500520-100500670	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr11:100500520-100500670	HCT-116	colon:	n/a	n/a
30	CTCF	chr11:100500540-100500690	GM12878	blood:	n/a	n/a
31	CTCF	chr11:100500509-100500630	NHEK	skin:	n/a	n/a
32	CTCF	chr11:100500531-100500613	A549	lung:	n/a	n/a
33	CTCF	chr11:100500460-100500610	K562	blood:	n/a	n/a
34	CTCF	chr11:100500480-100500630	GM12864	blood:	n/a	n/a
35	CTCF	chr11:100500540-100500690	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr11:100500480-100500630	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr11:100500520-100500670	HCFaa	heart:	n/a	n/a
38	CTCF	chr11:100500425-100500722	T-47D	breast:	n/a	n/a
39	CTCF	chr11:100500500-100500650	RPTEC	kidney:	n/a	n/a
40	CTCF	chr11:100500470-100500733	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:100500460-100500610	NHEK	skin:	n/a	n/a
42	CTCF	chr11:100500520-100500670	SAEC	small airway:	n/a	n/a
43	CTCF	chr11:100500480-100500630	Caco-2	colon:	n/a	n/a
44	CTCF	chr11:100500480-100500630	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr11:100500460-100500610	HRE	kidney:	n/a	n/a
46	CTCF	chr11:100500501-100500590	HepG2	liver:	n/a	n/a
47	CTCF	chr11:100500400-100500550	BE2_C	brain:	n/a	n/a
48	CTCF	chr11:100510580-100510730	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr11:100500513-100500651	GM12892	blood:	n/a	n/a
50	CTCF	chr11:100505820-100505970	GM12866	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:100502854-100502904	HRCEpiC	kidney:	n/a
2	chr11:100502854-100502904	HIPEpiC	eye:	n/a
3	chr11:100502854-100502904	MCF10A-Er-Src	breast:	n/a
4	chr11:100502854-100502904	HL-60	blood:	n/a
5	chr11:100502854-100502904	GM12892	blood:	n/a
6	chr11:100502854-100502904	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:100502854-100502904	ovcar-3	ovarian:	n/a
8	chr11:100502854-100502904	PANC-1	pancreas:	n/a
9	chr11:100502854-100502904	SKMC	muscle:	n/a
10	chr11:100502854-100502904	BJ	skin:	n/a
11	chr11:100502854-100502904	HEEpiC	esophagus:	n/a
12	chr11:100502854-100502904	HCM	heart:	n/a
13	chr11:100502854-100502904	GM19239	blood:	n/a
14	chr11:100502854-100502904	MCF-7	breast:	n/a
15	chr11:100502854-100502904	BE2_C	brain:	n/a
16	chr11:100502854-100502904	Jurkat	blood:	n/a
17	chr11:100502854-100502904	AG04449	skin:	fetal
18	chr11:100502854-100502904	ProgFib	skin:	n/a
19	chr11:100502854-100502904	RPTEC	kidney:	n/a
20	chr11:100502854-100502904	GM12891	blood:	n/a
21	chr11:100502854-100502904	AoSMC	blood vessel:	n/a
22	chr11:100502854-100502904	NHDF-neo	bronchial:	n/a
23	chr11:100502854-100502904	U87	brain:	n/a
24	chr11:100502854-100502904	T-47D	breast:	n/a
25	chr11:100502854-100502904	NHBE	bronchial:	n/a
26	chr11:100502854-100502904	HEK293	kidney:	embryo
27	chr11:100502854-100502904	AG04450	lung:	fetal
28	chr11:100502854-100502904	AG10803	skin:	n/a
29	chr11:100502854-100502904	HepG2	liver:	n/a
30	chr11:100502854-100502904	HCT-116	colon:	n/a
31	chr11:100502854-100502904	Hela-S3	cervix:	n/a
32	chr11:100502854-100502904	GM06990	blood:	n/a
33	chr11:100502854-100502904	K562	blood:	n/a
34	chr11:100502854-100502904	A549	lung:	n/a
35	chr11:100502854-100502904	SK-N-SH_RA	brain:	n/a
36	chr11:100502854-100502904	PrEC	prostate:	n/a
37	chr11:100502854-100502904	NB4	blood:	n/a
38	chr11:100502854-100502904	HNPCEpiC	eye:	n/a
39	chr11:100502854-100502904	NT2-D1	testis:	n/a
40	chr11:100502854-100502904	CMK	blood:	n/a
41	chr11:100502854-100502904	AG09309	skin:	n/a
42	chr11:100502854-100502904	HUVEC	blood vessel:	n/a
43	chr11:100502854-100502904	HRE	kidney:	n/a
44	chr11:100502854-100502904	HAEpiC	amniotic membrane:	n/a
45	chr11:100502854-100502904	AG09319	gingival:	n/a
46	chr11:100502854-100502904	HRPEpiC	eye:	n/a
47	chr11:100502854-100502904	GM12878	blood:	n/a
48	chr11:100502854-100502904	PFSK-1	brain:	n/a
49	chr11:100502854-100502904	Caco-2	colon:	n/a
50	chr11:100502854-100502904	ECC-1	luminal epithelium:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:100498644..100501937-chr11:100508407..100511533,3	K562	blood:
2	chr11:100500501..100502106-chr11:100540054..100542243,2	MCF-7	breast:
3	chr11:100498644..100501937-chr11:100508407..100511533,3	K562	blood:
4	chr11:100512317..100514358-chr11:100520283..100522609,2	K562	blood:
5	chr11:100483839..100486861-chr11:100501831..100504334,3	MCF-7	breast:
6	chr11:100509946..100512191-chr11:100577525..100580253,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PGR-6	chr11:100512709-100513004	NONHSAT023838

No data

Variant related genes	Relation type
RN7SL222P	TF binding region
RN7SL222P	CpG island
ENSG00000242165	chromatin interactions

Extended variants
information (count: 898 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:898 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs749433	chr11:100498709-100498710	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10894993	chr11:100498729-100498730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572154621	chr11:100498770-100498771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541273091	chr11:100498783-100498784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182432306	chr11:100498786-100498787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577674784	chr11:100498794-100498795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1393355	chr11:100498804-100498805	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs563348009	chr11:100498808-100498809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143074653	chr11:100498811-100498812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549304320	chr11:100498849-100498850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559859325	chr11:100498871-100498872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528684136	chr11:100498873-100498874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1393356	chr11:100498887-100498888	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs571862726	chr11:100498914-100498915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12286434	chr11:100498959-100498960	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs187793480	chr11:100499016-100499017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561185344	chr11:100499019-100499020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73580559	chr11:100499091-100499092	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs575312925	chr11:100499188-100499189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529811868	chr11:100499226-100499227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192220675	chr11:100499228-100499229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565839444	chr11:100499229-100499230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184954940	chr11:100499281-100499282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187827015	chr11:100499283-100499284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192113949	chr11:100499326-100499327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4309127	chr11:100499339-100499340	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs10894994	chr11:100499363-100499364	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs573690899	chr11:100499369-100499370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11224331	chr11:100499439-100499440	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs184326040	chr11:100499442-100499443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528651769	chr11:100499483-100499484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545307110	chr11:100499497-100499498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs67850267	chr11:100499503-100499504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6144477	chr11:100499507-100499508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201771155	chr11:100499511-100499512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200478426	chr11:100499512-100499513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531156604	chr11:100499577-100499578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4517480	chr11:100499627-100499628	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs181830566	chr11:100499689-100499690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184462096	chr11:100499705-100499706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11224332	chr11:100499725-100499726	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs77909238	chr11:100499729-100499730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs80223956	chr11:100499768-100499769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557712942	chr11:100499788-100499789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571554961	chr11:100499789-100499790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6590797	chr11:100499829-100499830	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs557298167	chr11:100499859-100499860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573654103	chr11:100499862-100499863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7932851	chr11:100499866-100499867	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs533467957	chr11:100499871-100499872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:100496200-100501600	Weak transcription	Placenta	Placenta
2	chr11:100500600-100500800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr11:100500600-100500800	Enhancers	Brain Substantia Nigra	brain
4	chr11:100500600-100500800	Enhancers	Fetal Brain Male	brain
5	chr11:100500600-100500800	Enhancers	Gastric	stomach
6	chr11:100500600-100500800	Enhancers	Left Ventricle	heart
7	chr11:100500600-100500800	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr11:100500600-100500800	Enhancers	K562	blood
9	chr11:100500600-100501000	Enhancers	Stomach Mucosa	stomach
10	chr11:100500600-100503400	Enhancers	Liver	Liver
11	chr11:100500800-100501400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr11:100500800-100501400	Weak transcription	Gastric	stomach
13	chr11:100500800-100501600	Weak transcription	Left Ventricle	heart
14	chr11:100500800-100501600	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr11:100500800-100501600	Weak transcription	K562	blood
16	chr11:100501000-100501400	Weak transcription	Stomach Mucosa	stomach
17	chr11:100501000-100503800	Weak transcription	Fetal Brain Male	brain
18	chr11:100501400-100502000	Enhancers	Gastric	stomach
19	chr11:100501400-100502200	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr11:100501400-100502400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr11:100501400-100502400	Enhancers	Fetal Intestine Large	intestine
22	chr11:100501400-100502600	Enhancers	Stomach Mucosa	stomach
23	chr11:100501400-100502800	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr11:100501600-100501800	Enhancers	Stomach Smooth Muscle	stomach
25	chr11:100501600-100502000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr11:100501600-100502000	Enhancers	Fetal Kidney	kidney
27	chr11:100501600-100502000	Enhancers	K562	blood
28	chr11:100501600-100502200	Enhancers	Fetal Lung	lung
29	chr11:100501600-100502400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr11:100501600-100502400	Enhancers	Fetal Muscle Leg	muscle
31	chr11:100501600-100502400	Enhancers	Left Ventricle	heart
32	chr11:100501600-100502400	Enhancers	Ovary	ovary
33	chr11:100501600-100502400	Enhancers	Right Atrium	heart
34	chr11:100501600-100502400	Enhancers	Right Ventricle	heart
35	chr11:100501600-100502400	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr11:100501600-100502400	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr11:100501600-100502400	Enhancers	Spleen	Spleen
38	chr11:100501600-100502600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr11:100501600-100504600	Enhancers	Placenta	Placenta
40	chr11:100501800-100502000	Enhancers	Adipose Nuclei	Adipose
41	chr11:100501800-100502000	Enhancers	Colon Smooth Muscle	Colon
42	chr11:100501800-100502000	Enhancers	Pancreas	Pancrea
43	chr11:100501800-100502200	Enhancers	H1 Cell Line	embryonic stem cell
44	chr11:100501800-100502200	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr11:100501800-100502400	Enhancers	Psoas Muscle	Psoas
46	chr11:100501800-100502600	Enhancers	Duodenum Mucosa	Duodenum
47	chr11:100501800-100502600	Enhancers	Fetal Intestine Small	intestine
48	chr11:100501800-100504200	Enhancers	Fetal Stomach	stomach
49	chr11:100501800-100506200	Enhancers	Fetal Heart	heart
50	chr11:100501800-100512200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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