Variant report

Variant	nsv834764
Chromosome Location	chr3:93518281-93677166
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:550)
CpG islands
(count:305)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:93560605-93560733	K562	blood:	n/a	n/a
2	ARID3A	chr3:93560633-93560810	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:93676282-93676501	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:93642022-93642172	K562	blood:	n/a	n/a
5	BATF	chr3:93655969-93656191	GM12878	blood:	n/a	n/a
6	CBX3	chr3:93560363-93560688	HCT-116	colon:	n/a	n/a
7	CBX3	chr3:93661017-93661284	K562	blood:	n/a	n/a
8	CBX3	chr3:93625948-93626194	K562	blood:	n/a	n/a
9	CBX3	chr3:93660944-93661275	K562	blood:	n/a	n/a
10	CEBPB	chr3:93560563-93560817	HepG2	liver:	n/a	n/a
11	CEBPB	chr3:93628924-93629461	Hela-S3	cervix:	n/a	chr3:93629160-93629171 chr3:93628939-93628950 chr3:93629159-93629172 chr3:93629159-93629170
12	CEBPB	chr3:93560451-93560821	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr3:93649629-93649633	K562	blood:	n/a	n/a
14	CEBPB	chr3:93560459-93560814	IMR90	lung:	n/a	n/a
15	CEBPB	chr3:93650673-93650708	K562	blood:	n/a	chr3:93650686-93650699 chr3:93650686-93650697
16	CEBPB	chr3:93574844-93574994	K562	blood:	n/a	n/a
17	CEBPB	chr3:93560562-93560819	K562	blood:	n/a	n/a
18	CEBPB	chr3:93560370-93560707	A549	lung:	n/a	n/a
19	CEBPB	chr3:93615540-93615692	K562	blood:	n/a	chr3:93615585-93615598
20	CEBPB	chr3:93629053-93629308	K562	blood:	n/a	chr3:93629160-93629171 chr3:93629159-93629172 chr3:93629159-93629170
21	CEBPB	chr3:93650513-93650709	HepG2	liver:	n/a	chr3:93650686-93650699 chr3:93650686-93650697
22	CEBPB	chr3:93577008-93577134	A549	lung:	n/a	n/a
23	CEBPB	chr3:93560514-93560789	A549	lung:	n/a	n/a
24	CEBPB	chr3:93629003-93629273	HepG2	liver:	n/a	chr3:93629160-93629171 chr3:93629159-93629172 chr3:93629159-93629170
25	CTCF	chr3:93586420-93586570	Hela-S3	cervix:	n/a	chr3:93586453-93586471
26	CTCF	chr3:93560569-93560806	Lung_OC	lung:	n/a	chr3:93560691-93560712 chr3:93560696-93560714
27	CTCF	chr3:93560500-93560650	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr3:93560541-93560753	A549	lung:	n/a	chr3:93560691-93560712 chr3:93560696-93560714
29	CTCF	chr3:93560700-93560850	NB4	blood:	n/a	n/a
30	CTCF	chr3:93560480-93560630	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr3:93600004-93600063	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr3:93560660-93560810	HPAF	blood vessel:	n/a	chr3:93560691-93560712 chr3:93560696-93560714
33	CTCF	chr3:93586423-93586509	H1-hESC	embryonic stem cell:	n/a	chr3:93586453-93586471
34	CTCF	chr3:93560480-93560630	NB4	blood:	n/a	n/a
35	CTCF	chr3:93657710-93657741	ProgFib	skin:	n/a	n/a
36	CTCF	chr3:93560600-93560750	HRE	kidney:	n/a	chr3:93560691-93560712 chr3:93560696-93560714
37	CTCF	chr3:93586380-93586530	SK-N-SH_RA	brain:	n/a	chr3:93586453-93586471
38	CTCF	chr3:93560620-93560770	SAEC	small airway:	n/a	chr3:93560691-93560712 chr3:93560696-93560714
39	CTCF	chr3:93560760-93560910	GM12866	blood:	n/a	n/a
40	CTCF	chr3:93560579-93560839	K562	blood:	n/a	chr3:93560691-93560712 chr3:93560696-93560714
41	CTCF	chr3:93560760-93560910	GM12865	blood:	n/a	n/a
42	CTCF	chr3:93586300-93586450	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr3:93586340-93586490	HMF	breast:	n/a	chr3:93586453-93586471
44	CTCF	chr3:93560700-93560850	HMEC	breast:	n/a	n/a
45	CTCF	chr3:93560592-93560791	ProgFib	skin:	n/a	chr3:93560691-93560712 chr3:93560696-93560714
46	CTCF	chr3:93560500-93560650	AG04450	lung:	n/a	n/a
47	CTCF	chr3:93520418-93520435	ProgFib	skin:	n/a	n/a
48	CTCF	chr3:93560544-93560845	Kidney_OC	kidney:	n/a	chr3:93560691-93560712 chr3:93560696-93560714
49	CTCF	chr3:93560500-93560650	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr3:93560780-93560930	GM12873	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:93646432-93646482	T-47D	breast:	n/a
2	chr3:93646432-93646482	ProgFib	skin:	n/a
3	chr3:93647007-93647057	NT2-D1	testis:	n/a
4	chr3:93592719-93592769	HL-60	blood:	n/a
5	chr3:93647007-93647057	AG04449	skin:	fetal
6	chr3:93646432-93646482	ovcar-3	ovarian:	n/a
7	chr3:93647605-93647655	NHDF-neo	bronchial:	n/a
8	chr3:93646432-93646482	AoSMC	blood vessel:	n/a
9	chr3:93646432-93646482	NT2-D1	testis:	n/a
10	chr3:93647007-93647057	HepG2	liver:	n/a
11	chr3:93592719-93592769	K562	blood:	n/a
12	chr3:93592719-93592769	BE2_C	brain:	n/a
13	chr3:93646432-93646482	U87	brain:	n/a
14	chr3:93592719-93592769	PFSK-1	brain:	n/a
15	chr3:93647605-93647655	ovcar-3	ovarian:	n/a
16	chr3:93646378-93646428	IMR90	lung:	fetal
17	chr3:93647605-93647655	HEEpiC	esophagus:	n/a
18	chr3:93592719-93592769	HMEC	breast:	n/a
19	chr3:93592719-93592769	HCPEpiC	choroid plexus:	n/a
20	chr3:93647007-93647057	A549	lung:	n/a
21	chr3:93592719-93592769	GM12878	blood:	n/a
22	chr3:93646432-93646482	HEEpiC	esophagus:	n/a
23	chr3:93647007-93647057	HAEpiC	amniotic membrane:	n/a
24	chr3:93646378-93646428	AG04449	skin:	fetal
25	chr3:93647007-93647057	HCM	heart:	n/a
26	chr3:93647007-93647057	ovcar-3	ovarian:	n/a
27	chr3:93646378-93646428	SAEC	small airway:	n/a
28	chr3:93647605-93647655	AG04449	skin:	fetal
29	chr3:93647007-93647057	BE2_C	brain:	n/a
30	chr3:93647007-93647057	HUVEC	blood vessel:	n/a
31	chr3:93647007-93647057	T-47D	breast:	n/a
32	chr3:93647605-93647655	HRCEpiC	kidney:	n/a
33	chr3:93592719-93592769	HAEpiC	amniotic membrane:	n/a
34	chr3:93646432-93646482	Hela-S3	cervix:	n/a
35	chr3:93592719-93592769	AG04450	lung:	fetal
36	chr3:93646378-93646428	CMK	blood:	n/a
37	chr3:93592719-93592769	HCT-116	colon:	n/a
38	chr3:93647007-93647057	SK-N-SH_RA	brain:	n/a
39	chr3:93592719-93592769	NHDF-neo	bronchial:	n/a
40	chr3:93592719-93592769	ovcar-3	ovarian:	n/a
41	chr3:93646378-93646428	Caco-2	colon:	n/a
42	chr3:93646432-93646482	NH-A	brain:	n/a
43	chr3:93646432-93646482	PANC-1	pancreas:	n/a
44	chr3:93647605-93647655	SK-N-SH_RA	brain:	n/a
45	chr3:93647605-93647655	NT2-D1	testis:	n/a
46	chr3:93646378-93646428	MCF10A-Er-Src	breast:	n/a
47	chr3:93592719-93592769	AG04449	skin:	fetal
48	chr3:93646378-93646428	SK-N-SH	brain:	n/a
49	chr3:93647007-93647057	U87	brain:	n/a
50	chr3:93646378-93646428	NH-A	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:93644215..93645979-chr3:93647690..93649933,2	K562	blood:
2	chr3:93571786..93573423-chr3:93699770..93701438,2	K562	blood:
3	chr3:93644215..93645979-chr3:93647690..93649933,2	K562	blood:
4	chr3:93650076..93652154-chr3:93653341..93655975,2	K562	blood:
5	chr3:93614459..93614996-chr5:160095807..160096625,2	MCF-7	breast:
6	chr3:93654201..93655762-chr3:93660898..93663750,2	MCF-7	breast:
7	chr3:93666583..93669103-chr3:93690628..93693616,3	MCF-7	breast:
8	chr3:93654201..93655762-chr3:93660898..93663750,2	MCF-7	breast:
9	chr3:93666897..93669716-chr3:93698788..93701503,2	K562	blood:
10	chr3:93675612..93678506-chr3:93691202..93693980,2	K562	blood:
11	chr3:93650076..93652154-chr3:93653341..93655975,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STX19-1	chr3:93624884-93624987	NONHSAT090718
2	lnc-STX19-1	chr3:93629463-93630001	NONHSAT090718

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PROS1	hsa-miR-335-5p	chr3:93592888-93592909

Variant related genes	Relation type
RNU6-488P	TF binding region
PROS1	TF binding region
RNU6-488P	CpG island
PROS1	CpG island
ENSG00000169379	chromatin interactions
ENSG00000184500	chromatin interactions

Extended variants
information (count: 4269 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:4269 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559347154	chr3:93518319-93518320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs142996886	chr3:93518336-93518337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551290900	chr3:93518359-93518360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs151115450	chr3:93518366-93518367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537576719	chr3:93518368-93518369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140951707	chr3:93518371-93518372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567850786	chr3:93518411-93518412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547748021	chr3:93518464-93518465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200796022	chr3:93518490-93518491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192472750	chr3:93518504-93518505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146333359	chr3:93518528-93518529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9835601	chr3:93518529-93518530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139156297	chr3:93518545-93518546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141617325	chr3:93518546-93518547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185315890	chr3:93518557-93518558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190312878	chr3:93518571-93518572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181619674	chr3:93518575-93518576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371926710	chr3:93518611-93518612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376856226	chr3:93518647-93518648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35755265	chr3:93518659-93518660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548305205	chr3:93518673-93518674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569991697	chr3:93518696-93518697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537153350	chr3:93518705-93518706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78999840	chr3:93518728-93518729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184906526	chr3:93518739-93518740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138011437	chr3:93518753-93518754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149507014	chr3:93518764-93518765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558624795	chr3:93518770-93518771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188521452	chr3:93518781-93518782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371285587	chr3:93518782-93518783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144175438	chr3:93518798-93518799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565324570	chr3:93518802-93518803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530879985	chr3:93518803-93518804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75902181	chr3:93518862-93518863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551062638	chr3:93518863-93518864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567619616	chr3:93518864-93518865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530336301	chr3:93518867-93518868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200669892	chr3:93518869-93518870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546904456	chr3:93518880-93518881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544652335	chr3:93518902-93518903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566705218	chr3:93518911-93518912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148269580	chr3:93518914-93518915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558823158	chr3:93518917-93518918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374673708	chr3:93518932-93518933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376062686	chr3:93518950-93518951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534873762	chr3:93518953-93518954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376279571	chr3:93518958-93518959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570916733	chr3:93518977-93518978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536604907	chr3:93518994-93518995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181048439	chr3:93519030-93519031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD

Chromatin state (count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:93516800-93519200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:93540600-93541400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:93558000-93558400	Enhancers	Osteobl	bone
4	chr3:93558200-93559200	Enhancers	Muscle Satellite Cultured Cells	--
5	chr3:93558400-93558800	Weak transcription	Osteobl	bone
6	chr3:93558600-93560200	Weak transcription	Psoas Muscle	Psoas
7	chr3:93558800-93559000	Enhancers	Osteobl	bone
8	chr3:93559000-93560200	Weak transcription	Osteobl	bone
9	chr3:93559200-93560200	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr3:93560000-93560200	Enhancers	Adipose Nuclei	Adipose
11	chr3:93560000-93560200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr3:93560000-93560200	Enhancers	Fetal Muscle Trunk	muscle
13	chr3:93560200-93560400	Enhancers	Primary B cells from peripheral blood	blood
14	chr3:93560200-93560400	Enhancers	Primary T cells fromperipheralblood	blood
15	chr3:93560200-93560400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr3:93560200-93560400	Enhancers	HUVEC	blood vessel
17	chr3:93560200-93560600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr3:93560200-93560600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr3:93560200-93560600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr3:93560200-93560600	Active TSS	Muscle Satellite Cultured Cells	--
21	chr3:93560200-93560600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr3:93560200-93560600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr3:93560200-93560600	Flanking Active TSS	Adipose Nuclei	Adipose
24	chr3:93560200-93560600	Active TSS	Aorta	Aorta
25	chr3:93560200-93560600	Flanking Active TSS	Liver	Liver
26	chr3:93560200-93560600	Active TSS	Brain Anterior Caudate	brain
27	chr3:93560200-93560600	Active TSS	Brain Inferior Temporal Lobe	brain
28	chr3:93560200-93560600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr3:93560200-93560600	Active TSS	Colon Smooth Muscle	Colon
30	chr3:93560200-93560600	Active TSS	Duodenum Mucosa	Duodenum
31	chr3:93560200-93560600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
32	chr3:93560200-93560600	Active TSS	Fetal Intestine Small	intestine
33	chr3:93560200-93560600	Flanking Active TSS	Fetal Muscle Trunk	muscle
34	chr3:93560200-93560600	Enhancers	Placenta	Placenta
35	chr3:93560200-93560600	Active TSS	Psoas Muscle	Psoas
36	chr3:93560200-93560600	Active TSS	Rectal Mucosa Donor 31	rectum
37	chr3:93560200-93560600	Active TSS	Rectal Smooth Muscle	rectum
38	chr3:93560200-93560600	Active TSS	Right Atrium	heart
39	chr3:93560200-93560600	Active TSS	Right Ventricle	heart
40	chr3:93560200-93560600	Active TSS	HMEC	breast
41	chr3:93560200-93560600	Active TSS	NH-A	brain
42	chr3:93560200-93560600	Active TSS	NHDF-Ad	bronchial
43	chr3:93560200-93560800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr3:93560200-93560800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr3:93560200-93560800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr3:93560200-93560800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
47	chr3:93560200-93560800	Active TSS	Primary T helper cells fromperipheralblood	blood
48	chr3:93560200-93560800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr3:93560200-93560800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr3:93560200-93560800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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