Variant report

Variant	esv13718
Chromosome Location	chr7:50860377-50861113
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	ATF3	chr7:50859958-50860389	K562	blood:	n/a	n/a
2	BACH1	chr7:50860949-50860952	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr7:50859682-50860388	K562	blood:	n/a	n/a
4	BRCA1	chr7:50859468-50860415	Hela-S3	cervix:	n/a	chr7:50860336-50860343
5	CCNT2	chr7:50860044-50861550	K562	blood:	n/a	chr7:50861156-50861165
6	CEBPB	chr7:50859711-50860399	HepG2	liver:	n/a	chr7:50859880-50859891 chr7:50859880-50859893 chr7:50859882-50859891 chr7:50859881-50859892
7	CEBPB	chr7:50859688-50860410	IMR90	lung:	n/a	chr7:50859880-50859891 chr7:50859880-50859893 chr7:50859882-50859891 chr7:50859881-50859892
8	CEBPB	chr7:50859234-50861061	Hela-S3	cervix:	n/a	chr7:50859880-50859891 chr7:50859880-50859893 chr7:50859882-50859891 chr7:50859881-50859892
9	CEBPB	chr7:50859644-50860396	MCF-7	breast:	n/a	chr7:50859880-50859891 chr7:50859880-50859893 chr7:50859882-50859891 chr7:50859881-50859892
10	CEBPB	chr7:50859697-50860386	A549	lung:	n/a	chr7:50859880-50859891 chr7:50859880-50859893 chr7:50859882-50859891 chr7:50859881-50859892
11	CEBPB	chr7:50859613-50860414	ECC-1	luminal epithelium:	n/a	chr7:50859880-50859891 chr7:50859880-50859893 chr7:50859882-50859891 chr7:50859881-50859892
12	CEBPB	chr7:50859572-50860416	MCF-7	breast:	n/a	chr7:50859880-50859891 chr7:50859880-50859893 chr7:50859882-50859891 chr7:50859881-50859892
13	CEBPB	chr7:50859547-50860431	K562	blood:	n/a	chr7:50859880-50859891 chr7:50859880-50859893 chr7:50859882-50859891 chr7:50859881-50859892
14	CEBPB	chr7:50859582-50860421	K562	blood:	n/a	chr7:50859880-50859891 chr7:50859880-50859893 chr7:50859882-50859891 chr7:50859881-50859892
15	CEBPB	chr7:50859476-50860435	A549	lung:	n/a	chr7:50859880-50859891 chr7:50859880-50859893 chr7:50859882-50859891 chr7:50859881-50859892
16	CEBPD	chr7:50859617-50860449	K562	blood:	n/a	chr7:50859880-50859891
17	CEBPD	chr7:50859598-50860471	K562	blood:	n/a	chr7:50859880-50859891
18	CHD2	chr7:50860028-50860613	K562	blood:	n/a	n/a
19	CHD2	chr7:50859731-50861451	Hela-S3	cervix:	n/a	chr7:50860608-50860618 chr7:50859934-50859944
20	CREB1	chr7:50860408-50860692	A549	lung:	n/a	n/a
21	CTCF	chr7:50860440-50860590	NHDF-neo	bronchial:	n/a	n/a
22	CTCF	chr7:50861040-50861190	Caco-2	colon:	n/a	n/a
23	CTCF	chr7:50860557-50860664	Hela-S3	cervix:	n/a	chr7:50860614-50860623
24	CTCF	chr7:50860558-50860678	MCF-7	breast:	n/a	chr7:50860614-50860623
25	CTCF	chr7:50860520-50860670	AG04449	skin:	n/a	chr7:50860614-50860623
26	CTCF	chr7:50860500-50860650	AoAF	blood vessel:	n/a	chr7:50860614-50860623
27	CTCF	chr7:50860580-50860730	RPTEC	kidney:	n/a	chr7:50860614-50860623
28	CTCF	chr7:50860595-50860648	K562	blood:	n/a	chr7:50860614-50860623
29	CTCF	chr7:50860904-50860958	NHEK	skin:	n/a	chr7:50860941-50860954
30	CTCF	chr7:50860540-50860690	HRPEpiC	eye:	n/a	chr7:50860614-50860623
31	CTCF	chr7:50860960-50861040	K562	blood:	n/a	n/a
32	CTCF	chr7:50860520-50860670	HUVEC	blood vessel:	n/a	chr7:50860614-50860623
33	CTCF	chr7:50860520-50860670	HEK293	kidney:	n/a	chr7:50860614-50860623
34	CTCF	chr7:50860595-50860630	MCF-7	breast:	n/a	chr7:50860614-50860623
35	CTCF	chr7:50860574-50860652	K562	blood:	n/a	chr7:50860614-50860623
36	CTCF	chr7:50860608-50860635	MCF-7	breast:	n/a	chr7:50860614-50860623
37	CTCF	chr7:50860520-50860670	HA-sp	spinal cord:	n/a	chr7:50860614-50860623
38	CTCF	chr7:50860540-50860690	HCPEpiC	choroid plexus:	n/a	chr7:50860614-50860623
39	CTCF	chr7:50860934-50860980	Hela-S3	cervix:	n/a	chr7:50860941-50860954
40	CTCF	chr7:50860581-50860640	MCF-7	breast:	n/a	chr7:50860614-50860623
41	CTCF	chr7:50860618-50860622	IMR90	lung:	n/a	n/a
42	CTCF	chr7:50860855-50861032	MCF-7	breast:	n/a	chr7:50860941-50860954
43	CTCF	chr7:50860500-50860650	SAEC	small airway:	n/a	chr7:50860614-50860623
44	CTCF	chr7:50860520-50860670	HPAF	blood vessel:	n/a	chr7:50860614-50860623
45	CTCF	chr7:50860878-50861003	MCF-7	breast:	n/a	chr7:50860941-50860954
46	CTCF	chr7:50860800-50860950	SAEC	small airway:	n/a	n/a
47	CTCF	chr7:50860540-50860690	AG09319	gingival:	n/a	chr7:50860614-50860623
48	CTCF	chr7:50860500-50860650	K562	blood:	n/a	chr7:50860614-50860623
49	CTCF	chr7:50861037-50861038	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:50860500-50860650	HBMEC	blood vessel:	n/a	chr7:50860614-50860623

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:50860564-50860614	SAEC	small airway:	n/a
2	chr7:50860564-50860614	SAEC	small airway:	n/a
3	chr7:50860866-50860916	NT2-D1	testis:	n/a
4	chr7:50860564-50860614	HAEpiC	amniotic membrane:	n/a
5	chr7:50860872-50860922	GM19239	blood:	n/a
6	chr7:50861049-50861099	AG09309	skin:	n/a
7	chr7:50860564-50860614	Jurkat	blood:	n/a
8	chr7:50860866-50860916	GM12892	blood:	n/a
9	chr7:50860564-50860614	NHDF-neo	bronchial:	n/a
10	chr7:50860564-50860614	A549	lung:	n/a
11	chr7:50860872-50860922	HRE	kidney:	n/a
12	chr7:50861049-50861099	CMK	blood:	n/a
13	chr7:50860872-50860922	NT2-D1	testis:	n/a
14	chr7:50860564-50860614	PFSK-1	brain:	n/a
15	chr7:50860564-50860614	ovcar-3	ovarian:	n/a
16	chr7:50860872-50860922	A549	lung:	n/a
17	chr7:50861049-50861099	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:50860866-50860916	BE2_C	brain:	n/a
19	chr7:50860872-50860922	CMK	blood:	n/a
20	chr7:50860872-50860922	IMR90	lung:	fetal
21	chr7:50861049-50861099	BE2_C	brain:	n/a
22	chr7:50860564-50860614	AG04449	skin:	fetal
23	chr7:50861049-50861099	BJ	skin:	n/a
24	chr7:50860564-50860614	GM12878	blood:	n/a
25	chr7:50860872-50860922	AG09319	gingival:	n/a
26	chr7:50860866-50860916	SK-N-SH_RA	brain:	n/a
27	chr7:50860564-50860614	NB4	blood:	n/a
28	chr7:50860564-50860614	SK-N-SH_RA	brain:	n/a
29	chr7:50860866-50860916	ProgFib	skin:	n/a
30	chr7:50860564-50860614	HCF	heart:	n/a
31	chr7:50860564-50860614	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:50861049-50861099	Caco-2	colon:	n/a
33	chr7:50861049-50861099	GM12892	blood:	n/a
34	chr7:50860866-50860916	HIPEpiC	eye:	n/a
35	chr7:50860872-50860922	HCPEpiC	choroid plexus:	n/a
36	chr7:50860872-50860922	HIPEpiC	eye:	n/a
37	chr7:50861049-50861099	U87	brain:	n/a
38	chr7:50860872-50860922	HPAEpiC	pulmonary alveolar:	n/a
39	chr7:50860872-50860922	NHBE	bronchial:	n/a
40	chr7:50860866-50860916	H1-hESC	embryonic stem cell:	embryo
41	chr7:50861049-50861099	GM06990	blood:	n/a
42	chr7:50860866-50860916	MCF10A-Er-Src	breast:	n/a
43	chr7:50861049-50861099	PANC-1	pancreas:	n/a
44	chr7:50860564-50860614	AG10803	skin:	n/a
45	chr7:50860872-50860922	U87	brain:	n/a
46	chr7:50860872-50860922	HEEpiC	esophagus:	n/a
47	chr7:50860866-50860916	AG09309	skin:	n/a
48	chr7:50860872-50860922	AG09309	skin:	n/a
49	chr7:50861049-50861099	HCPEpiC	choroid plexus:	n/a
50	chr7:50860564-50860614	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:159848892..159849860-chr7:50860666..50861462,2	NB4	blood:
2	chr7:50820026..50825124-chr7:50858182..50862797,5	K562	blood:
3	chr7:50672342..50675062-chr7:50858858..50861329,2	K562	blood:
4	chr7:50799534..50801547-chr7:50859929..50861719,2	K562	blood:
5	chr7:50814324..50816744-chr7:50859392..50862105,3	K562	blood:
6	chr7:50823624..50825816-chr7:50859906..50861742,2	K562	blood:
7	chr7:50859012..50860567-chr7:50873879..50876072,2	K562	blood:
8	chr1:165797659..165798365-chr7:50859677..50860628,2	Hela-S3	cervix:

Variant related genes	Relation type
GRB10	TF binding region
GRB10	CpG island
ENSG00000106070	chromatin interactions
ENSG00000164611	chromatin interactions

Extended variants
information (count: 16 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115306625	chr7:50860409-50860410	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs553281590	chr7:50860428-50860429	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs181986615	chr7:50860444-50860445	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs541029873	chr7:50860449-50860450	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150178389	chr7:50860491-50860492	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs574791488	chr7:50860571-50860572	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs543503748	chr7:50860619-50860620	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs563576658	chr7:50860620-50860621	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs78954264	chr7:50860635-50860636	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs138644022	chr7:50860639-50860640	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs149306056	chr7:50860648-50860649	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs559761828	chr7:50860657-50860658	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs528098611	chr7:50860660-50860661	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs547829382	chr7:50860691-50860692	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs568045568	chr7:50860827-50860828	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs537183425	chr7:50860916-50860917	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50857200-50861800	Active TSS	Right Atrium	heart
2	chr7:50857400-50861800	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr7:50858200-50861600	Active TSS	Left Ventricle	heart
4	chr7:50858400-50860400	Flanking Active TSS	Adipose Nuclei	Adipose
5	chr7:50858800-50860600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:50858800-50861800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:50858800-50861800	Active TSS	Pancreas	Pancrea
8	chr7:50859000-50860400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr7:50859200-50861400	Active TSS	Esophagus	oesophagus
10	chr7:50859200-50861600	Active TSS	Lung	lung
11	chr7:50859200-50861800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:50859400-50860400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr7:50859400-50860400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
14	chr7:50859400-50860400	Active TSS	Brain Substantia Nigra	brain
15	chr7:50859400-50861400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
16	chr7:50859400-50861600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr7:50859400-50861600	Active TSS	Aorta	Aorta
18	chr7:50859400-50861600	Active TSS	Fetal Kidney	kidney
19	chr7:50859400-50861600	Active TSS	Ovary	ovary
20	chr7:50859400-50861600	Active TSS	Psoas Muscle	Psoas
21	chr7:50859400-50861600	Active TSS	Right Ventricle	heart
22	chr7:50859400-50861800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:50859400-50861800	Bivalent/Poised TSS	Thymus	Thymus
24	chr7:50859400-50861800	Bivalent/Poised TSS	HepG2	liver
25	chr7:50859400-50861800	Active TSS	HSMM	muscle
26	chr7:50859600-50860400	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
27	chr7:50859600-50860400	Active TSS	Fetal Lung	lung
28	chr7:50859600-50860600	Flanking Active TSS	Primary hematopoietic stem cells	blood
29	chr7:50859600-50860600	Active TSS	Colon Smooth Muscle	Colon
30	chr7:50859600-50860600	Active TSS	NHDF-Ad	bronchial
31	chr7:50859600-50861400	Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr7:50859600-50861400	Active TSS	HUES6 Cell Line	embryonic stem cell
33	chr7:50859600-50861400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr7:50859600-50861400	Active TSS	Cortex derived primary cultured neurospheres	brain
35	chr7:50859600-50861400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr7:50859600-50861400	Active TSS	K562	blood
37	chr7:50859600-50861600	Active TSS	HSMMtube	muscle
38	chr7:50859600-50861800	Active TSS	H9 Cell Line	embryonic stem cell
39	chr7:50859600-50861800	Bivalent/Poised TSS	HMEC	breast
40	chr7:50859800-50860400	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
41	chr7:50859800-50860400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
42	chr7:50859800-50860400	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
43	chr7:50859800-50860600	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr7:50859800-50860600	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
45	chr7:50859800-50861000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr7:50859800-50861000	Active TSS	Spleen	Spleen
47	chr7:50859800-50861400	Active TSS	H1 Cell Line	embryonic stem cell
48	chr7:50859800-50861400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr7:50859800-50861400	Active TSS	Hela-S3	cervix
50	chr7:50859800-50861400	Active TSS	HUVEC	blood vessel

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