Variant report

Variant	nsv880425
Chromosome Location	chr5:52291279-52345868
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:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:52283580..52285693-chr5:52296693..52299370,2	MCF-7	breast:
2	chr5:52288695..52291271-chr5:52292952..52294743,2	MCF-7	breast:
3	chr5:52318784..52321169-chr5:52323561..52325105,2	K562	blood:
4	chr5:52299602..52301517-chr5:52301947..52304132,2	MCF-7	breast:
5	chr5:52285332..52287022-chr5:52289921..52292396,2	MCF-7	breast:
6	chr5:52283450..52286797-chr5:52300386..52302948,4	MCF-7	breast:
7	chr5:52285803..52288356-chr5:52293284..52295985,2	MCF-7	breast:
8	chr5:52287570..52290507-chr5:52297245..52299058,2	MCF-7	breast:
9	chr5:52326404..52328383-chr5:52333260..52335027,2	MCF-7	breast:
10	chr5:52283546..52286213-chr5:52315102..52316776,2	MCF-7	breast:
11	chr5:52342580..52344559-chr5:52347867..52350544,2	K562	blood:
12	chr5:52287901..52290762-chr5:52300870..52303377,2	MCF-7	breast:
13	chr5:52284537..52287438-chr5:52289001..52291401,4	MCF-7	breast:
14	chr5:52319764..52321344-chr5:52327151..52329228,2	K562	blood:
15	chr5:52326404..52328383-chr5:52333260..52335027,2	MCF-7	breast:
16	chr5:52299602..52301517-chr5:52301947..52304132,2	MCF-7	breast:
17	chr5:52285122..52287993-chr5:52333837..52337640,3	MCF-7	breast:
18	chr5:52318784..52321169-chr5:52323561..52325105,2	K562	blood:
19	chr5:52284387..52286666-chr5:52306077..52309238,3	MCF-7	breast:
20	chr5:52298353..52300154-chr5:52302167..52303725,2	K562	blood:
21	chr5:52243837..52246026-chr5:52316094..52318313,2	MCF-7	breast:
22	chr5:52340133..52343071-chr5:52343982..52345648,2	K562	blood:
23	chr17:62236129..62238534-chr5:52321834..52323811,2	MCF-7	breast:
24	chr5:52319764..52321344-chr5:52327151..52329228,2	K562	blood:
25	chr5:52313064..52315275-chr5:52327348..52329688,2	MCF-7	breast:
26	chr5:52313064..52315275-chr5:52327348..52329688,2	MCF-7	breast:
27	chr5:52340133..52343071-chr5:52343982..52345648,2	K562	blood:
28	chr5:52298353..52300154-chr5:52302167..52303725,2	K562	blood:
29	chr5:52283964..52286344-chr5:52303235..52304989,2	MCF-7	breast:
30	chr5:52284308..52287113-chr5:52321640..52324132,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000249899	chromatin interactions
ENSG00000164171	chromatin interactions

Extended variants
information (count: 1905 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1905 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35234	chr5:52291279-52291280	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189608120	chr5:52291345-52291346	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs371592677	chr5:52291353-52291354	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs58231501	chr5:52291397-52291398	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs548961368	chr5:52291446-52291447	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs376637437	chr5:52291484-52291485	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs114087348	chr5:52291491-52291492	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs368824463	chr5:52291520-52291521	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs149582752	chr5:52291528-52291529	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs549571264	chr5:52291539-52291540	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs571082063	chr5:52291544-52291545	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs542652248	chr5:52291545-52291546	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs562627342	chr5:52291564-52291565	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538940338	chr5:52291594-52291595	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs181210933	chr5:52291621-52291622	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs565943418	chr5:52291633-52291634	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs536294637	chr5:52291646-52291647	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs186661740	chr5:52291689-52291690	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576619395	chr5:52291779-52291780	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs531732649	chr5:52291797-52291798	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs144297056	chr5:52291833-52291834	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189863260	chr5:52291872-52291873	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs542746674	chr5:52291895-52291896	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs560721878	chr5:52291899-52291900	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577329514	chr5:52291904-52291905	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs62357201	chr5:52291949-52291950	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs559822281	chr5:52292071-52292072	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541578036	chr5:52292114-52292115	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372441913	chr5:52292117-52292118	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs186081331	chr5:52292127-52292128	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs542270003	chr5:52292152-52292153	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs3212659	chr5:52292167-52292168	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs35235	chr5:52292237-52292238	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs3212391	chr5:52292405-52292406	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs547395148	chr5:52292406-52292407	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs148446090	chr5:52292454-52292455	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs3212392	chr5:52292477-52292478	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs35236	chr5:52292555-52292556	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs547568047	chr5:52292571-52292572	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs3212660	chr5:52292619-52292620	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs529959510	chr5:52292682-52292683	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs552389760	chr5:52292686-52292687	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs3212393	chr5:52292702-52292703	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs3212661	chr5:52292723-52292724	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs563266741	chr5:52292739-52292740	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs559126369	chr5:52292804-52292805	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs143638568	chr5:52292834-52292835	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs183429167	chr5:52292840-52292841	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs147206099	chr5:52292849-52292850	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs3212394	chr5:52292983-52292984	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1315 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52286200-52295400	Weak transcription	Pancreas	Pancrea
2	chr5:52286200-52300400	Weak transcription	Gastric	stomach
3	chr5:52286200-52303400	Weak transcription	Small Intestine	intestine
4	chr5:52286200-52313600	Weak transcription	Lung	lung
5	chr5:52286600-52292000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr5:52286600-52292600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr5:52286600-52293400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr5:52286600-52300000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr5:52286600-52302400	Weak transcription	Fetal Stomach	stomach
10	chr5:52286800-52294400	Weak transcription	Osteobl	bone
11	chr5:52286800-52298800	Weak transcription	Fetal Intestine Large	intestine
12	chr5:52287000-52292200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr5:52287000-52293000	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr5:52287000-52293400	Weak transcription	Fetal Intestine Small	intestine
15	chr5:52287000-52299400	Weak transcription	Duodenum Mucosa	Duodenum
16	chr5:52287200-52292600	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr5:52287200-52293200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:52287200-52293400	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr5:52287200-52293600	Weak transcription	Fetal Kidney	kidney
20	chr5:52288000-52292400	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
21	chr5:52288800-52292000	Enhancers	NHDF-Ad	bronchial
22	chr5:52289000-52291600	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
23	chr5:52289200-52311600	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr5:52289400-52292000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr5:52289400-52295600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:52290000-52292800	Enhancers	Brain Anterior Caudate	brain
27	chr5:52290000-52299800	Weak transcription	NH-A	brain
28	chr5:52290200-52291600	Enhancers	Hela-S3	cervix
29	chr5:52290400-52291600	Genic enhancers	NHEK	skin
30	chr5:52290600-52291800	Transcr. at gene 5' and 3'	HepG2	liver
31	chr5:52290600-52292400	Enhancers	Brain Angular Gyrus	brain
32	chr5:52290600-52294400	Weak transcription	NHLF	lung
33	chr5:52290800-52291600	Enhancers	Spleen	Spleen
34	chr5:52290800-52292200	Genic enhancers	HMEC	breast
35	chr5:52290800-52293000	Enhancers	Brain Hippocampus Middle	brain
36	chr5:52290800-52293200	Enhancers	Brain Cingulate Gyrus	brain
37	chr5:52290800-52293200	Weak transcription	HUVEC	blood vessel
38	chr5:52291000-52291600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr5:52291000-52291600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr5:52291000-52291800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr5:52291000-52292400	Enhancers	Esophagus	oesophagus
42	chr5:52291000-52292800	Enhancers	A549	lung
43	chr5:52291000-52295600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr5:52291200-52291400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr5:52291200-52291400	Flanking Active TSS	Brain Substantia Nigra	brain
46	chr5:52291200-52291600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr5:52291400-52291800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr5:52291400-52293600	Enhancers	Brain Substantia Nigra	brain
49	chr5:52291600-52291800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr5:52291600-52291800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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