Variant report

Variant	nsv1048543
Chromosome Location	chr13:64264234-64373228
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:183)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:183 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr13:64313524-64313659	HepG2	liver:	n/a	chr13:64313555-64313566
2	CEBPB	chr13:64282710-64282910	H1-hESC	embryonic stem cell:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
3	CEBPB	chr13:64282619-64282952	IMR90	lung:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
4	CEBPB	chr13:64282631-64282951	HepG2	liver:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
5	CTCF	chr13:64338496-64338540	ProgFib	skin:	n/a	n/a
6	CTCF	chr13:64324126-64324196	HUVEC	blood vessel:	n/a	n/a
7	CTCF	chr13:64320948-64321033	LNCaP	prostate:	n/a	n/a
8	CTCF	chr13:64343509-64343605	GM20000	blood:	n/a	n/a
9	CTCF	chr13:64324092-64324260	MCF-7	breast:	n/a	n/a
10	CTCF	chr13:64324052-64324317	LNCaP	prostate:	n/a	n/a
11	CTCF	chr13:64324197-64324224	GM19240	blood:	n/a	n/a
12	CTCF	chr13:64281020-64281170	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr13:64330314-64330384	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr13:64324125-64324255	Fibrobl	skin:	n/a	n/a
15	CTCF	chr13:64324080-64324269	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr13:64281060-64281210	HCT-116	colon:	n/a	n/a
17	CTCF	chr13:64334444-64334532	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr13:64343244-64343298	GM13976	blood:	n/a	n/a
19	CTCF	chr13:64324072-64324260	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr13:64297739-64297766	LNCaP	prostate:	n/a	n/a
21	CTCF	chr13:64312154-64312170	GM20000	blood:	n/a	n/a
22	CTCF	chr13:64324119-64324214	GM10248	blood:	n/a	n/a
23	CTCF	chr13:64320841-64320933	LNCaP	prostate:	n/a	n/a
24	CTCF	chr13:64324118-64324236	GM13977	blood:	n/a	n/a
25	CTCF	chr13:64324173-64324251	GM12878	blood:	n/a	n/a
26	CTCF	chr13:64338648-64338715	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr13:64356700-64356850	HepG2	liver:	n/a	n/a
28	CTCF	chr13:64324050-64324261	MCF-7	breast:	n/a	n/a
29	CTCF	chr13:64324028-64324296	A549	lung:	n/a	n/a
30	CTCF	chr13:64324133-64324259	MCF-7	breast:	n/a	n/a
31	CTCF	chr13:64324146-64324249	GM19238	blood:	n/a	n/a
32	CTCF	chr13:64296335-64296399	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr13:64324047-64324270	Medullo	brain:	n/a	n/a
34	CTCF	chr13:64292400-64292402	Lung_OC	lung:	n/a	n/a
35	CTCF	chr13:64324040-64324265	HepG2	liver:	n/a	n/a
36	CTCF	chr13:64324117-64324248	GM10266	blood:	n/a	n/a
37	CTCF	chr13:64324034-64324271	MCF-7	breast:	n/a	n/a
38	CTCF	chr13:64324024-64324308	K562	blood:	n/a	n/a
39	CTCF	chr13:64338203-64338280	GM13976	blood:	n/a	n/a
40	CTCF	chr13:64324108-64324265	MCF-7	breast:	n/a	n/a
41	CTCF	chr13:64338485-64338489	ProgFib	skin:	n/a	n/a
42	CTCF	chr13:64292407-64292528	Lung_OC	lung:	n/a	n/a
43	CTCF	chr13:64324094-64324161	K562	blood:	n/a	n/a
44	CTCF	chr13:64324079-64324211	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr13:64328827-64328856	LNCaP	prostate:	n/a	n/a
46	CTCF	chr13:64324183-64324225	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr13:64330862-64330927	Medullo	brain:	n/a	n/a
48	CTCF	chr13:64339091-64339163	Lung_OC	lung:	n/a	n/a
49	CTCF	chr13:64324133-64324244	ProgFib	skin:	n/a	n/a
50	CTCF	chr13:64324128-64324253	GM19239	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:64311555-64311605	PANC-1	pancreas:	n/a
2	chr13:64315383-64315433	RPTEC	kidney:	n/a
3	chr13:64315383-64315433	AG09319	gingival:	n/a
4	chr13:64311555-64311605	SK-N-SH	brain:	n/a
5	chr13:64311397-64311447	GM12891	blood:	n/a
6	chr13:64311555-64311605	SAEC	small airway:	n/a
7	chr13:64311555-64311605	HCPEpiC	choroid plexus:	n/a
8	chr13:64311397-64311447	HCPEpiC	choroid plexus:	n/a
9	chr13:64311555-64311605	GM12892	blood:	n/a
10	chr13:64311555-64311605	HIPEpiC	eye:	n/a
11	chr13:64311397-64311447	HUVEC	blood vessel:	n/a
12	chr13:64315383-64315433	SK-N-MC	brain:	n/a
13	chr13:64311397-64311447	BJ	skin:	n/a
14	chr13:64311555-64311605	CMK	blood:	n/a
15	chr13:64315383-64315433	Hela-S3	cervix:	n/a
16	chr13:64311555-64311605	HEK293	kidney:	embryo
17	chr13:64311397-64311447	HRCEpiC	kidney:	n/a
18	chr13:64311555-64311605	Jurkat	blood:	n/a
19	chr13:64315383-64315433	NH-A	brain:	n/a
20	chr13:64311397-64311447	HCF	heart:	n/a
21	chr13:64311555-64311605	HNPCEpiC	eye:	n/a
22	chr13:64311397-64311447	HPAEpiC	pulmonary alveolar:	n/a
23	chr13:64311555-64311605	IMR90	lung:	fetal
24	chr13:64311397-64311447	HepG2	liver:	n/a
25	chr13:64315383-64315433	BE2_C	brain:	n/a
26	chr13:64311555-64311605	NB4	blood:	n/a
27	chr13:64315383-64315433	SAEC	small airway:	n/a
28	chr13:64315383-64315433	HCPEpiC	choroid plexus:	n/a
29	chr13:64311397-64311447	HEK293	kidney:	embryo
30	chr13:64311397-64311447	RPTEC	kidney:	n/a
31	chr13:64315383-64315433	HAEpiC	amniotic membrane:	n/a
32	chr13:64315383-64315433	PrEC	prostate:	n/a
33	chr13:64311397-64311447	HIPEpiC	eye:	n/a
34	chr13:64311555-64311605	HCM	heart:	n/a
35	chr13:64311397-64311447	BE2_C	brain:	n/a
36	chr13:64311555-64311605	AG04450	lung:	fetal
37	chr13:64311397-64311447	PANC-1	pancreas:	n/a
38	chr13:64311555-64311605	LNCaP	prostate:	n/a
39	chr13:64311397-64311447	HL-60	blood:	n/a
40	chr13:64315383-64315433	Caco-2	colon:	n/a
41	chr13:64311397-64311447	K562	blood:	n/a
42	chr13:64311555-64311605	NT2-D1	testis:	n/a
43	chr13:64311397-64311447	LNCaP	prostate:	n/a
44	chr13:64311397-64311447	ProgFib	skin:	n/a
45	chr13:64311397-64311447	HCM	heart:	n/a
46	chr13:64315383-64315433	AG04450	lung:	fetal
47	chr13:64315383-64315433	NT2-D1	testis:	n/a
48	chr13:64315383-64315433	HIPEpiC	eye:	n/a
49	chr13:64311397-64311447	SK-N-SH	brain:	n/a
50	chr13:64315383-64315433	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:64303686..64305846-chr13:64306387..64309282,2	MCF-7	breast:
2	chr13:64303686..64305846-chr13:64306387..64309282,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH20-9	chr13:64303522-64303642	XLOC_010643
2	lnc-PCDH20-9	chr13:64291083-64291151	XLOC_010643
3	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034175
4	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034173
5	lnc-AL445989.1-20	chr13:64314899-64315042	NONHSAT034173
6	lnc-PCDH20-9	chr13:64288485-64288508	XLOC_010643
7	lnc-AL445989.1-20	chr13:64313246-64314310	NONHSAT034174
8	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034174
9	lnc-PCDH20-9	chr13:64312042-64312151	XLOC_010643
10	lnc-AL445989.1-1	chr13:64324837-64325213	ENSG00000237378
11	lnc-PCDH20-9	chr13:64303522-64303895	XLOC_010643
12	lnc-AL445989.1-20	chr13:64316498-64316945	NONHSAT034176
13	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034172
14	lnc-PCDH20-9	chr13:64301184-64301215	XLOC_010643
15	lnc-AL445989.1-20	chr13:64311843-64312482	NONHSAT034172
16	lnc-AL445989.1-1	chr13:64322132-64322530	ENSG00000237378
17	lnc-AL445989.1-20	chr13:64314899-64315042	NONHSAT034174
18	lnc-AL445989.1-20	chr13:64311843-64312416	NONHSAT034173
19	lnc-AL445989.1-20	chr13:64313246-64314376	NONHSAT034175

No data

Variant related genes	Relation type
LINC00395	TF binding region
ENSG00000226974	TF binding region
ENSG00000237378	TF binding region
RNU6-81P	TF binding region
OR7E156P	TF binding region
LINC00395	CpG island
ENSG00000226974	CpG island
ENSG00000237378	CpG island
RNU6-81P	CpG island
OR7E156P	CpG island
DUSP3	miRNA target sites

Extended variants
information (count: 888 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:888 , 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	rs532380176	chr13:64274210-64274211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs550923744	chr13:64274248-64274249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569267162	chr13:64274253-64274254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536705709	chr13:64274295-64274296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546944485	chr13:64274332-64274333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140191855	chr13:64274346-64274347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs375100883	chr13:64274366-64274367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76091503	chr13:64274476-64274477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558873311	chr13:64274497-64274498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577183344	chr13:64274558-64274559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537460969	chr13:64274578-64274579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556081611	chr13:64274580-64274581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574449301	chr13:64274638-64274639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541902803	chr13:64274715-64274716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554780693	chr13:64274729-64274730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs117539543	chr13:64274752-64274753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540552550	chr13:64274766-64274767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565257986	chr13:64274767-64274768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2810801	chr13:64274794-64274795	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs544285244	chr13:64274802-64274803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562899609	chr13:64274803-64274804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114436733	chr13:64274807-64274808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572277528	chr13:64274849-64274850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186160836	chr13:64274889-64274890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2590909	chr13:64274948-64274949	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs78184913	chr13:64274962-64274963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571833393	chr13:64275007-64275008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147745056	chr13:64275023-64275024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77975704	chr13:64275029-64275030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538095525	chr13:64275031-64275032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555931146	chr13:64275117-64275118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540682386	chr13:64275126-64275127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs114399142	chr13:64275127-64275128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149199951	chr13:64275130-64275131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs9571004	chr13:64275133-64275134	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs189859097	chr13:64275171-64275172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2590910	chr13:64275172-64275173	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs142397305	chr13:64275178-64275179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562777830	chr13:64275193-64275194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536547161	chr13:64279219-64279220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554645605	chr13:64279233-64279234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs56788467	chr13:64279253-64279254	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs192632190	chr13:64279292-64279293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536059752	chr13:64279347-64279348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576834016	chr13:64279383-64279384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112097014	chr13:64279418-64279419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs57575727	chr13:64279443-64279444	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs59659820	chr13:64279456-64279457	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs549252970	chr13:64279468-64279469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs36069041	chr13:64279475-64279476	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:64274200-64275000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:64274400-64274800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:64274400-64275000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr13:64274600-64275200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr13:64279200-64279600	Enhancers	Fetal Brain Male	brain
6	chr13:64302400-64302800	Enhancers	Fetal Intestine Small	intestine
7	chr13:64302400-64303200	Enhancers	Fetal Intestine Large	intestine
8	chr13:64302800-64303800	Weak transcription	Fetal Intestine Small	intestine
9	chr13:64303200-64303600	Weak transcription	Fetal Intestine Large	intestine
10	chr13:64303600-64303800	Enhancers	Fetal Intestine Large	intestine
11	chr13:64303800-64304400	Enhancers	Fetal Intestine Small	intestine
12	chr13:64303800-64305800	Weak transcription	Fetal Intestine Large	intestine
13	chr13:64304400-64305800	Weak transcription	Fetal Intestine Small	intestine
14	chr13:64305600-64306000	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr13:64305800-64306200	Enhancers	HepG2	liver
16	chr13:64305800-64306600	Enhancers	Fetal Intestine Large	intestine
17	chr13:64305800-64306600	Enhancers	Stomach Mucosa	stomach
18	chr13:64305800-64307200	Enhancers	Fetal Intestine Small	intestine
19	chr13:64306000-64307800	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr13:64306200-64307000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr13:64307800-64308200	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr13:64308200-64310200	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr13:64310200-64310600	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr13:64315400-64316200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr13:64347400-64348200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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