Variant report

Variant	esv1837793
Chromosome Location	chr11:24443570-24527958
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	ATF2	chr11:24518353-24518812	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr11:24518327-24518833	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr11:24518280-24518908	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr11:24499284-24499616	IMR90	lung:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
5	CEBPB	chr11:24499282-24499587	Hela-S3	cervix:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
6	CEBPB	chr11:24502399-24502754	IMR90	lung:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
7	CEBPB	chr11:24502419-24502734	Hela-S3	cervix:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
8	CEBPB	chr11:24504500-24504875	MCF-7	breast:	n/a	chr11:24504658-24504667 chr11:24504658-24504667 chr11:24504656-24504669 chr11:24504658-24504667
9	CEBPB	chr11:24518479-24518656	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr11:24504498-24504929	MCF-7	breast:	n/a	chr11:24504658-24504667 chr11:24504658-24504667 chr11:24504656-24504669 chr11:24504658-24504667
11	CEBPB	chr11:24502446-24502730	H1-hESC	embryonic stem cell:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
12	CEBPB	chr11:24502444-24502712	A549	lung:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
13	CEBPB	chr11:24500295-24500561	HepG2	liver:	n/a	chr11:24500481-24500492
14	CEBPB	chr11:24499426-24499477	H1-hESC	embryonic stem cell:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
15	CEBPB	chr11:24459325-24459347	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr11:24524696-24525212	MCF-7	breast:	n/a	n/a
17	CEBPB	chr11:24500310-24500645	IMR90	lung:	n/a	chr11:24500481-24500492
18	CEBPB	chr11:24487951-24488156	A549	lung:	n/a	chr11:24488014-24488027
19	CEBPB	chr11:24504492-24504816	A549	lung:	n/a	chr11:24504658-24504667 chr11:24504658-24504667 chr11:24504656-24504669 chr11:24504658-24504667
20	CEBPB	chr11:24502417-24502754	ECC-1	luminal epithelium:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
21	CEBPB	chr11:24459132-24459434	HepG2	liver:	n/a	chr11:24459283-24459294
22	CEBPB	chr11:24499285-24499610	HepG2	liver:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
23	CEBPB	chr11:24500312-24500613	Hela-S3	cervix:	n/a	chr11:24500481-24500492
24	CEBPB	chr11:24499285-24499571	A549	lung:	n/a	chr11:24499435-24499448 chr11:24499435-24499446 chr11:24499436-24499447 chr11:24499437-24499446
25	CEBPB	chr11:24502393-24502740	HepG2	liver:	n/a	chr11:24502572-24502581 chr11:24502570-24502583 chr11:24502572-24502581 chr11:24502572-24502581
26	CEBPB	chr11:24459149-24459440	IMR90	lung:	n/a	chr11:24459283-24459294
27	CHD1	chr11:24518674-24518698	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr11:24518563-24518933	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTBP2	chr11:24518245-24518979	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr11:24518700-24518850	SAEC	small airway:	n/a	n/a
31	CTCF	chr11:24518689-24518883	LNCaP	prostate:	n/a	n/a
32	CTCF	chr11:24457340-24457490	RPTEC	kidney:	n/a	n/a
33	CTCF	chr11:24518648-24518918	Gliobla	brain:	n/a	n/a
34	CTCF	chr11:24518960-24519110	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr11:24518720-24518870	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr11:24518629-24518933	MCF-7	breast:	n/a	n/a
37	CTCF	chr11:24458720-24458870	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr11:24505305-24505625	MCF-7	breast:	n/a	chr11:24505408-24505424
39	CTCF	chr11:24458740-24458967	MCF-7	breast:	n/a	n/a
40	CTCF	chr11:24518680-24518830	AG04450	lung:	n/a	n/a
41	CTCF	chr11:24505340-24505483	MCF-7	breast:	n/a	chr11:24505408-24505424
42	CTCF	chr11:24518940-24519090	HAc	cerebellar:	n/a	n/a
43	CTCF	chr11:24458803-24458913	HepG2	liver:	n/a	n/a
44	CTCF	chr11:24518380-24518530	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr11:24458780-24458930	Caco-2	colon:	n/a	n/a
46	CTCF	chr11:24458820-24458970	MCF-7	breast:	n/a	n/a
47	CTCF	chr11:24518620-24518770	SAEC	small airway:	n/a	n/a
48	CTCF	chr11:24518760-24518910	HMEC	breast:	n/a	n/a
49	CTCF	chr11:24518700-24518850	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr11:24458760-24458910	HRE	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:24518367-24518417	NT2-D1	testis:	n/a
2	chr11:24518367-24518417	NT2-D1	testis:	n/a
3	chr11:24469509-24469559	NHBE	bronchial:	n/a
4	chr11:24518374-24518424	HIPEpiC	eye:	n/a
5	chr11:24518776-24518826	ovcar-3	ovarian:	n/a
6	chr11:24518379-24518429	HCF	heart:	n/a
7	chr11:24518414-24518464	HRCEpiC	kidney:	n/a
8	chr11:24518367-24518417	HCPEpiC	choroid plexus:	n/a
9	chr11:24518737-24518787	HNPCEpiC	eye:	n/a
10	chr11:24518894-24518944	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:24518776-24518826	Hepatocyte	liver:	n/a
12	chr11:24518894-24518944	K562	blood:	n/a
13	chr11:24518381-24518431	IMR90	lung:	fetal
14	chr11:24518281-24518331	HPAEpiC	pulmonary alveolar:	n/a
15	chr11:24518367-24518417	AG10803	skin:	n/a
16	chr11:24518281-24518331	GM12892	blood:	n/a
17	chr11:24518374-24518424	T-47D	breast:	n/a
18	chr11:24518225-24518275	K562	blood:	n/a
19	chr11:24518448-24518498	NT2-D1	testis:	n/a
20	chr11:24469509-24469559	HCPEpiC	choroid plexus:	n/a
21	chr11:24518225-24518275	BJ	skin:	n/a
22	chr11:24518894-24518944	HCT-116	colon:	n/a
23	chr11:24518737-24518787	HAEpiC	amniotic membrane:	n/a
24	chr11:24518414-24518464	PANC-1	pancreas:	n/a
25	chr11:24518225-24518275	HNPCEpiC	eye:	n/a
26	chr11:24518225-24518275	AG09309	skin:	n/a
27	chr11:24518776-24518826	PrEC	prostate:	n/a
28	chr11:24518381-24518431	HPAEpiC	pulmonary alveolar:	n/a
29	chr11:24518379-24518429	ProgFib	skin:	n/a
30	chr11:24518414-24518464	HRE	kidney:	n/a
31	chr11:24518381-24518431	AG09319	gingival:	n/a
32	chr11:24518374-24518424	GM06990	blood:	n/a
33	chr11:24518281-24518331	T-47D	breast:	n/a
34	chr11:24518225-24518275	ovcar-3	ovarian:	n/a
35	chr11:24518776-24518826	HUVEC	blood vessel:	n/a
36	chr11:24518149-24518199	HMEC	breast:	n/a
37	chr11:24518374-24518424	ovcar-3	ovarian:	n/a
38	chr11:24518448-24518498	A549	lung:	n/a
39	chr11:24518281-24518331	CMK	blood:	n/a
40	chr11:24518776-24518826	IMR90	lung:	fetal
41	chr11:24518448-24518498	MCF10A-Er-Src	breast:	n/a
42	chr11:24518149-24518199	GM12878	blood:	n/a
43	chr11:24469509-24469559	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:24518737-24518787	NHDF-neo	bronchial:	n/a
45	chr11:24518374-24518424	HEEpiC	esophagus:	n/a
46	chr11:24518367-24518417	BE2_C	brain:	n/a
47	chr11:24518414-24518464	PFSK-1	brain:	n/a
48	chr11:24518367-24518417	Caco-2	colon:	n/a
49	chr11:24518414-24518464	NHBE	bronchial:	n/a
50	chr11:24518149-24518199	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:24516764..24518659-chr11:24525705..24528388,2	K562	blood:
2	chr10:67189751..67190645-chr11:24504879..24505471,2	MCF-7	breast:

Variant related genes	Relation type
LUZP2	TF binding region
ENSG00000207252	TF binding region
LUZP2	CpG island
ENSG00000207252	CpG island
ENSG00000187398	chromatin interactions

Extended variants
information (count: 1109 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1109 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12279193	chr11:24443570-24443571	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575776631	chr11:24443577-24443578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186993746	chr11:24443596-24443597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554758153	chr11:24443614-24443615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374743068	chr11:24443673-24443674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545112803	chr11:24443678-24443679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143476694	chr11:24443686-24443687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576805626	chr11:24443695-24443696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545447275	chr11:24443707-24443708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146822030	chr11:24443718-24443719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531257529	chr11:24443719-24443720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550769471	chr11:24443746-24443747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138872868	chr11:24443755-24443756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530231783	chr11:24443769-24443770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs36066006	chr11:24443805-24443806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142851298	chr11:24443831-24443832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115121060	chr11:24443898-24443899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567039388	chr11:24443948-24443949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539040627	chr11:24443951-24443952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552577640	chr11:24444059-24444060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569377265	chr11:24444087-24444088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34039242	chr11:24444091-24444092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543169483	chr11:24449723-24449724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546628506	chr11:24449738-24449739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372977404	chr11:24449750-24449751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs117618669	chr11:24449755-24449756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190348042	chr11:24449770-24449771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537800784	chr11:24449778-24449779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559093396	chr11:24449811-24449812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145033643	chr11:24449829-24449830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538024503	chr11:24449837-24449838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554865022	chr11:24449840-24449841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs113233149	chr11:24449854-24449855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147555734	chr11:24449862-24449863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182902037	chr11:24449878-24449879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186346658	chr11:24449894-24449895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191594677	chr11:24449896-24449897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576426610	chr11:24449898-24449899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527794902	chr11:24449900-24449901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142085153	chr11:24449905-24449906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562227897	chr11:24449907-24449908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531022966	chr11:24449943-24449944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs199894091	chr11:24449961-24449962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556205165	chr11:24449982-24449983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12418983	chr11:24449998-24449999	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs561627414	chr11:24450044-24450045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530287322	chr11:24450057-24450058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182514955	chr11:24450114-24450115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs118016881	chr11:24450116-24450117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532531123	chr11:24450142-24450143	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24443000-24444200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr11:24443200-24443600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr11:24443200-24443600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr11:24443200-24443600	Enhancers	HMEC	breast
5	chr11:24443200-24444000	Enhancers	NHEK	skin
6	chr11:24449600-24450000	Enhancers	Fetal Intestine Large	intestine
7	chr11:24449800-24450200	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr11:24464600-24467600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
9	chr11:24465400-24466800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr11:24465800-24466200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr11:24465800-24467000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
12	chr11:24465800-24467200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
13	chr11:24465800-24467800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
14	chr11:24466000-24467600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
15	chr11:24466400-24467600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
16	chr11:24467200-24469200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr11:24467400-24471200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr11:24467600-24468600	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr11:24467600-24468600	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr11:24467600-24469000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr11:24467800-24470600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr11:24468600-24471600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr11:24468600-24471600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr11:24469000-24471000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr11:24469200-24470000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr11:24469200-24470600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr11:24469400-24470200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr11:24470000-24470800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr11:24470600-24471000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr11:24470800-24471200	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr11:24474800-24475600	Enhancers	Hela-S3	cervix
32	chr11:24477400-24478000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
33	chr11:24479200-24479600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr11:24479200-24480800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr11:24482200-24483200	Enhancers	Brain Substantia Nigra	brain
36	chr11:24482600-24482800	Enhancers	Brain Hippocampus Middle	brain
37	chr11:24482600-24483000	Enhancers	Brain Cingulate Gyrus	brain
38	chr11:24483200-24483600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr11:24485400-24485800	Enhancers	Adipose Nuclei	Adipose
40	chr11:24485600-24486400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr11:24485600-24486400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr11:24486000-24486400	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr11:24499200-24499800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr11:24499200-24500400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr11:24511200-24511600	Enhancers	HepG2	liver
46	chr11:24517200-24517400	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr11:24517200-24518800	Active TSS	Brain Angular Gyrus	brain
48	chr11:24517200-24519200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
49	chr11:24517200-24519600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
50	chr11:24517400-24517800	Active TSS	Breast Myoepithelial Primary Cells	Breast

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