Variant report

Variant	nsv980150
Chromosome Location	chr4:119499004-119514502
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:642)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:642 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:119507675-119507759	K562	blood:	n/a	n/a
2	ARID3A	chr4:119512536-119512865	K562	blood:	n/a	n/a
3	ARID3A	chr4:119512561-119512966	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:119506782-119507225	K562	blood:	n/a	n/a
5	ATF1	chr4:119512070-119513121	K562	blood:	n/a	n/a
6	ATF2	chr4:119512614-119513118	H1-hESC	embryonic stem cell:	n/a	chr4:119512938-119512949
7	ATF2	chr4:119512592-119513106	H1-hESC	embryonic stem cell:	n/a	chr4:119512938-119512949
8	ATF2	chr4:119512454-119513054	GM12878	blood:	n/a	chr4:119512938-119512949
9	ATF2	chr4:119512613-119513089	GM12878	blood:	n/a	chr4:119512938-119512949
10	ATF3	chr4:119512767-119512947	GM12878	blood:	n/a	n/a
11	ATF3	chr4:119512712-119513009	HepG2	liver:	n/a	chr4:119512939-119512959 chr4:119512938-119512951
12	ATF3	chr4:119512562-119513118	H1-hESC	embryonic stem cell:	n/a	chr4:119512939-119512959 chr4:119512938-119512951
13	ATF3	chr4:119512604-119513031	HepG2	liver:	n/a	chr4:119512939-119512959 chr4:119512938-119512951
14	ATF3	chr4:119512720-119513004	K562	blood:	n/a	chr4:119512939-119512959 chr4:119512938-119512951
15	ATF3	chr4:119512726-119513024	GM12878	blood:	n/a	chr4:119512939-119512959 chr4:119512938-119512951
16	ATF3	chr4:119512715-119513024	K562	blood:	n/a	chr4:119512939-119512959 chr4:119512938-119512951
17	ATF3	chr4:119512622-119513034	H1-hESC	embryonic stem cell:	n/a	chr4:119512939-119512959 chr4:119512938-119512951
18	ATF3	chr4:119512508-119513020	K562	blood:	n/a	chr4:119512939-119512959 chr4:119512938-119512951
19	BACH1	chr4:119512429-119512706	K562	blood:	n/a	n/a
20	BATF	chr4:119512730-119513339	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:119512789-119513378	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:119512396-119513016	K562	blood:	n/a	n/a
23	BHLHE40	chr4:119512528-119512917	GM12878	blood:	n/a	n/a
24	BRCA1	chr4:119512677-119513029	GM12878	blood:	n/a	n/a
25	BRCA1	chr4:119512666-119513025	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr4:119512297-119513077	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr4:119512486-119513039	HepG2	liver:	n/a	n/a
28	CBX3	chr4:119512471-119513394	K562	blood:	n/a	n/a
29	CBX3	chr4:119512472-119513060	K562	blood:	n/a	n/a
30	CCNT2	chr4:119512727-119513012	K562	blood:	n/a	n/a
31	CEBPB	chr4:119507010-119507321	MCF-7	breast:	n/a	n/a
32	CEBPB	chr4:119507030-119507405	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr4:119512539-119513232	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:119507055-119507393	IMR90	lung:	n/a	n/a
35	CEBPB	chr4:119512544-119513304	A549	lung:	n/a	n/a
36	CEBPB	chr4:119507028-119507289	K562	blood:	n/a	n/a
37	CEBPB	chr4:119506946-119507639	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr4:119506981-119507362	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr4:119512499-119513354	K562	blood:	n/a	n/a
40	CEBPB	chr4:119507036-119507645	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:119503207-119503383	IMR90	lung:	n/a	chr4:119503298-119503307
42	CEBPB	chr4:119512545-119513304	K562	blood:	n/a	n/a
43	CEBPB	chr4:119506854-119507706	K562	blood:	n/a	n/a
44	CEBPD	chr4:119512803-119513297	K562	blood:	n/a	n/a
45	CEBPD	chr4:119512767-119513133	HepG2	liver:	n/a	n/a
46	CHD1	chr4:119512605-119512972	GM12878	blood:	n/a	n/a
47	CHD2	chr4:119512696-119513056	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr4:119512482-119513011	GM12878	blood:	n/a	n/a
49	CHD2	chr4:119512676-119513021	K562	blood:	n/a	n/a
50	CHD2	chr4:119512645-119513027	Hela-S3	cervix:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:119512985-119513035	T-47D	breast:	n/a
2	chr4:119506870-119506920	RPTEC	kidney:	n/a
3	chr4:119506870-119506920	NB4	blood:	n/a
4	chr4:119512985-119513035	AG04450	lung:	fetal
5	chr4:119506870-119506920	HCT-116	colon:	n/a
6	chr4:119512985-119513035	LNCaP	prostate:	n/a
7	chr4:119512985-119513035	SK-N-SH_RA	brain:	n/a
8	chr4:119512985-119513035	AoSMC	blood vessel:	n/a
9	chr4:119506870-119506920	NHDF-neo	bronchial:	n/a
10	chr4:119512985-119513035	PANC-1	pancreas:	n/a
11	chr4:119512985-119513035	AG09309	skin:	n/a
12	chr4:119506870-119506920	HL-60	blood:	n/a
13	chr4:119512985-119513035	BE2_C	brain:	n/a
14	chr4:119506870-119506920	A549	lung:	n/a
15	chr4:119506870-119506920	PFSK-1	brain:	n/a
16	chr4:119506870-119506920	HNPCEpiC	eye:	n/a
17	chr4:119512985-119513035	A549	lung:	n/a
18	chr4:119512985-119513035	MCF-7	breast:	n/a
19	chr4:119512985-119513035	AG04449	skin:	fetal
20	chr4:119512985-119513035	ovcar-3	ovarian:	n/a
21	chr4:119512985-119513035	Caco-2	colon:	n/a
22	chr4:119512985-119513035	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:119506870-119506920	Caco-2	colon:	n/a
24	chr4:119512985-119513035	U87	brain:	n/a
25	chr4:119512985-119513035	GM12892	blood:	n/a
26	chr4:119512985-119513035	SK-N-SH	brain:	n/a
27	chr4:119512985-119513035	PrEC	prostate:	n/a
28	chr4:119512985-119513035	HCF	heart:	n/a
29	chr4:119512985-119513035	NHBE	bronchial:	n/a
30	chr4:119506870-119506920	NH-A	brain:	n/a
31	chr4:119512985-119513035	Hepatocyte	liver:	n/a
32	chr4:119512985-119513035	HL-60	blood:	n/a
33	chr4:119506870-119506920	HRPEpiC	eye:	n/a
34	chr4:119512985-119513035	Jurkat	blood:	n/a
35	chr4:119506870-119506920	GM12891	blood:	n/a
36	chr4:119512985-119513035	AG10803	skin:	n/a
37	chr4:119512985-119513035	HRE	kidney:	n/a
38	chr4:119506870-119506920	T-47D	breast:	n/a
39	chr4:119512985-119513035	SAEC	small airway:	n/a
40	chr4:119512985-119513035	HCM	heart:	n/a
41	chr4:119506870-119506920	H1-hESC	embryonic stem cell:	embryo
42	chr4:119506870-119506920	SAEC	small airway:	n/a
43	chr4:119506870-119506920	HCF	heart:	n/a
44	chr4:119512985-119513035	HNPCEpiC	eye:	n/a
45	chr4:119506870-119506920	HAEpiC	amniotic membrane:	n/a
46	chr4:119512985-119513035	HCPEpiC	choroid plexus:	n/a
47	chr4:119506870-119506920	K562	blood:	n/a
48	chr4:119506870-119506920	MCF-7	breast:	n/a
49	chr4:119512985-119513035	ProgFib	skin:	n/a
50	chr4:119512985-119513035	NT2-D1	testis:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:119503145..119504877-chr4:119508741..119511511,2	K562	blood:
2	chr4:119505891..119507633-chr4:119509359..119512309,2	MCF-7	breast:
3	chr4:119505891..119507633-chr4:119509359..119512309,2	MCF-7	breast:
4	chr4:119503145..119504877-chr4:119508741..119511511,2	K562	blood:
5	chr4:119508532..119510926-chr4:119602289..119604089,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000260404	TF binding region
ENSG00000260404	CpG island

Extended variants
information (count: 429 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115203734	chr4:119504037-119504038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559913121	chr4:119504041-119504042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529388462	chr4:119504078-119504079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111670044	chr4:119504086-119504087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568915248	chr4:119504098-119504099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531705597	chr4:119504117-119504118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551805913	chr4:119504149-119504150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs193028766	chr4:119504153-119504154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568634780	chr4:119504155-119504156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112770953	chr4:119504156-119504157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554450924	chr4:119504173-119504174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567849502	chr4:119504222-119504223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35890030	chr4:119504232-119504233	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs555453294	chr4:119504274-119504275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs72676188	chr4:119504280-119504281	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs13120874	chr4:119504291-119504292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571858641	chr4:119504294-119504295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112636560	chr4:119504295-119504296	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
19	rs567914967	chr4:119504297-119504298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs70941185	chr4:119504337-119504338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12331154	chr4:119504339-119504340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs59796281	chr4:119504347-119504348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12331732	chr4:119504354-119504355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536653652	chr4:119504356-119504357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12331454	chr4:119504371-119504372	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs28707145	chr4:119504428-119504429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs28408071	chr4:119504430-119504431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371615510	chr4:119504436-119504437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190517491	chr4:119504437-119504438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375887263	chr4:119504438-119504439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368955350	chr4:119504439-119504440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76226861	chr4:119504571-119504572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182225555	chr4:119504687-119504688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540127585	chr4:119504709-119504710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559927109	chr4:119504763-119504764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76147784	chr4:119504809-119504810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183753662	chr4:119504862-119504863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542737551	chr4:119504904-119504905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562969077	chr4:119504949-119504950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531699962	chr4:119505015-119505016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551783021	chr4:119505030-119505031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188468148	chr4:119505093-119505094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528025197	chr4:119505105-119505106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368001950	chr4:119505106-119505107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548068679	chr4:119505129-119505130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532165922	chr4:119505130-119505131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370798777	chr4:119505144-119505145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140980605	chr4:119505168-119505169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527292248	chr4:119505223-119505224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549113474	chr4:119505254-119505255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Autism	19246517	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119504000-119507000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:119505200-119506000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:119505200-119506800	Enhancers	K562	blood
4	chr4:119505400-119505800	Active TSS	Duodenum Mucosa	Duodenum
5	chr4:119505600-119505800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr4:119505600-119506800	Enhancers	Liver	Liver
7	chr4:119505800-119506000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr4:119505800-119506000	Enhancers	Hela-S3	cervix
9	chr4:119505800-119506200	Enhancers	GM12878-XiMat	blood
10	chr4:119505800-119506800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:119505800-119506800	Enhancers	Ovary	ovary
12	chr4:119505800-119507000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:119505800-119507800	Enhancers	Duodenum Mucosa	Duodenum
14	chr4:119506000-119506200	Bivalent Enhancer	NHDF-Ad	bronchial
15	chr4:119506000-119506400	Enhancers	Fetal Muscle Trunk	muscle
16	chr4:119506000-119506400	Enhancers	Fetal Muscle Leg	muscle
17	chr4:119506000-119506400	Enhancers	Left Ventricle	heart
18	chr4:119506000-119506600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:119506000-119506600	Weak transcription	Hela-S3	cervix
20	chr4:119506000-119506800	Enhancers	H1 Cell Line	embryonic stem cell
21	chr4:119506000-119506800	Enhancers	H9 Cell Line	embryonic stem cell
22	chr4:119506000-119506800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr4:119506000-119508000	Enhancers	Pancreas	Pancrea
24	chr4:119506200-119506600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr4:119506400-119506600	Weak transcription	Left Ventricle	heart
26	chr4:119506400-119506600	Bivalent Enhancer	Osteobl	bone
27	chr4:119506400-119506800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr4:119506400-119506800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr4:119506400-119507400	Enhancers	Stomach Mucosa	stomach
30	chr4:119506400-119507800	Enhancers	Placenta	Placenta
31	chr4:119506400-119508000	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr4:119506600-119506800	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr4:119506600-119506800	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr4:119506600-119506800	Enhancers	Osteobl	bone
35	chr4:119506600-119507000	Enhancers	Left Ventricle	heart
36	chr4:119506600-119507200	Enhancers	Hela-S3	cervix
37	chr4:119506600-119507400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr4:119506600-119508000	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr4:119506600-119512800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:119506800-119507000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr4:119506800-119507000	Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr4:119506800-119507000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr4:119506800-119507000	Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr4:119506800-119507000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr4:119506800-119507000	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--
46	chr4:119506800-119507200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
47	chr4:119506800-119507200	Active TSS	H9 Cell Line	embryonic stem cell
48	chr4:119506800-119507200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr4:119506800-119507200	Active TSS	HUES64 Cell Line	embryonic stem cell
50	chr4:119506800-119507200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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