Variant report

Variant	esv3317859
Chromosome Location	chr19:52136165-52150513
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:282)
CpG islands
(count:305)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:52140651-52140961	K562	blood:	n/a	n/a
2	BATF	chr19:52149947-52150214	GM12878	blood:	n/a	n/a
3	BCL11A	chr19:52149937-52150305	GM12878	blood:	n/a	n/a
4	BHLHE40	chr19:52150049-52150408	GM12878	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
5	BHLHE40	chr19:52147812-52147863	K562	blood:	n/a	n/a
6	BHLHE40	chr19:52150088-52150405	K562	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
7	CBX3	chr19:52140579-52140964	K562	blood:	n/a	n/a
8	CBX3	chr19:52140595-52141003	K562	blood:	n/a	n/a
9	CEBPB	chr19:52144983-52145193	IMR90	lung:	n/a	chr19:52145111-52145122
10	CEBPB	chr19:52144942-52145259	A549	lung:	n/a	chr19:52145111-52145122
11	CEBPB	chr19:52145000-52145199	K562	blood:	n/a	chr19:52145111-52145122
12	CEBPB	chr19:52144962-52145257	HepG2	liver:	n/a	chr19:52145111-52145122
13	CTCF	chr19:52140442-52141373	A549	lung:	n/a	n/a
14	CTCF	chr19:52140760-52140910	AG09309	skin:	n/a	n/a
15	CTCF	chr19:52140700-52140850	K562	blood:	n/a	n/a
16	CTCF	chr19:52140741-52140925	GM10266	blood:	n/a	n/a
17	CTCF	chr19:52140723-52140918	A549	lung:	n/a	n/a
18	CTCF	chr19:52140900-52141050	NHDF-neo	bronchial:	n/a	n/a
19	CTCF	chr19:52140777-52140845	LNCaP	prostate:	n/a	n/a
20	CTCF	chr19:52140780-52140930	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr19:52140800-52140950	GM12872	blood:	n/a	n/a
22	CTCF	chr19:52140740-52140890	GM12869	blood:	n/a	n/a
23	CTCF	chr19:52140729-52140884	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr19:52140700-52140850	HVMF	connective:	n/a	n/a
25	CTCF	chr19:52140720-52140870	AG04449	skin:	n/a	n/a
26	CTCF	chr19:52140760-52140910	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr19:52140720-52140870	HMEC	breast:	n/a	n/a
28	CTCF	chr19:52140720-52140870	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr19:52140960-52141110	WI-38	lung:	n/a	n/a
30	CTCF	chr19:52140808-52140906	NHEK	skin:	n/a	n/a
31	CTCF	chr19:52140760-52140910	SAEC	small airway:	n/a	n/a
32	CTCF	chr19:52140840-52140990	A549	lung:	n/a	n/a
33	CTCF	chr19:52140340-52140490	GM12875	blood:	n/a	n/a
34	CTCF	chr19:52140760-52140910	GM12864	blood:	n/a	n/a
35	CTCF	chr19:52140800-52140950	GM12878	blood:	n/a	n/a
36	CTCF	chr19:52140740-52140890	GM12874	blood:	n/a	n/a
37	CTCF	chr19:52140740-52140890	NHLF	lung:	n/a	n/a
38	CTCF	chr19:52140720-52140870	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr19:52140740-52140890	AG10803	skin:	n/a	n/a
40	CTCF	chr19:52140760-52140910	GM12865	blood:	n/a	n/a
41	CTCF	chr19:52140797-52140906	MCF-7	breast:	n/a	n/a
42	CTCF	chr19:52140680-52140830	GM12878	blood:	n/a	n/a
43	CTCF	chr19:52140607-52141021	MCF-7	breast:	n/a	n/a
44	CTCF	chr19:52140740-52140890	HCFaa	heart:	n/a	n/a
45	CTCF	chr19:52140675-52140967	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr19:52140740-52140897	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr19:52140660-52140810	BJ	skin:	n/a	n/a
48	CTCF	chr19:52140760-52140910	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr19:52140720-52140870	HepG2	liver:	n/a	n/a
50	CTCF	chr19:52140656-52140963	IMR90	lung:	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	chr19:52140097-52140147	BE2_C	brain:	n/a
2	chr19:52146598-52146648	NB4	blood:	n/a
3	chr19:52148354-52148404	H1-hESC	embryonic stem cell:	embryo
4	chr19:52148354-52148404	T-47D	breast:	n/a
5	chr19:52140097-52140147	RPTEC	kidney:	n/a
6	chr19:52150233-52150283	NHDF-neo	bronchial:	n/a
7	chr19:52150233-52150283	SK-N-MC	brain:	n/a
8	chr19:52146598-52146648	HNPCEpiC	eye:	n/a
9	chr19:52148354-52148404	K562	blood:	n/a
10	chr19:52140097-52140147	BJ	skin:	n/a
11	chr19:52148354-52148404	U87	brain:	n/a
12	chr19:52140097-52140147	HRE	kidney:	n/a
13	chr19:52146598-52146648	CMK	blood:	n/a
14	chr19:52148354-52148404	GM06990	blood:	n/a
15	chr19:52150233-52150283	BJ	skin:	n/a
16	chr19:52148354-52148404	HL-60	blood:	n/a
17	chr19:52150230-52150280	HRPEpiC	eye:	n/a
18	chr19:52140097-52140147	HL-60	blood:	n/a
19	chr19:52150233-52150283	Hela-S3	cervix:	n/a
20	chr19:52150233-52150283	HCM	heart:	n/a
21	chr19:52150233-52150283	HCPEpiC	choroid plexus:	n/a
22	chr19:52148354-52148404	HRCEpiC	kidney:	n/a
23	chr19:52150233-52150283	U87	brain:	n/a
24	chr19:52140097-52140147	AG04450	lung:	fetal
25	chr19:52148354-52148404	PANC-1	pancreas:	n/a
26	chr19:52148354-52148404	NHDF-neo	bronchial:	n/a
27	chr19:52150230-52150280	HL-60	blood:	n/a
28	chr19:52146598-52146648	K562	blood:	n/a
29	chr19:52146598-52146648	HUVEC	blood vessel:	n/a
30	chr19:52150230-52150280	Hepatocyte	liver:	n/a
31	chr19:52150233-52150283	SKMC	muscle:	n/a
32	chr19:52148354-52148404	SK-N-SH_RA	brain:	n/a
33	chr19:52148354-52148404	ProgFib	skin:	n/a
34	chr19:52150230-52150280	GM12891	blood:	n/a
35	chr19:52150233-52150283	AoSMC	blood vessel:	n/a
36	chr19:52150230-52150280	HCM	heart:	n/a
37	chr19:52146598-52146648	HCT-116	colon:	n/a
38	chr19:52148354-52148404	PrEC	prostate:	n/a
39	chr19:52150230-52150280	MCF10A-Er-Src	breast:	n/a
40	chr19:52150233-52150283	LNCaP	prostate:	n/a
41	chr19:52150230-52150280	HPAEpiC	pulmonary alveolar:	n/a
42	chr19:52146598-52146648	HepG2	liver:	n/a
43	chr19:52148354-52148404	HCPEpiC	choroid plexus:	n/a
44	chr19:52148354-52148404	HAEpiC	amniotic membrane:	n/a
45	chr19:52150230-52150280	U87	brain:	n/a
46	chr19:52150233-52150283	NT2-D1	testis:	n/a
47	chr19:52150230-52150280	NH-A	brain:	n/a
48	chr19:52140097-52140147	AG10803	skin:	n/a
49	chr19:52150230-52150280	GM19239	blood:	n/a
50	chr19:52148354-52148404	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:52110923..52111673-chr19:52140530..52141292,3	MCF-7	breast:
2	chr19:51960903..51963783-chr19:52139621..52141126,2	K562	blood:
3	chr19:51978649..51980839-chr19:52139351..52142005,2	K562	blood:
4	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
5	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
6	chr19:52050848..52053096-chr19:52143769..52145532,2	K562	blood:
7	chr19:52110942..52111788-chr19:52140328..52140831,2	K562	blood:
8	chr19:51975813..51976889-chr19:52140105..52142089,6	K562	blood:
9	chr19:52140352..52141294-chr19:52160036..52160673,2	K562	blood:
10	chr19:52017645..52019212-chr19:52145235..52147486,2	MCF-7	breast:
11	chr19:51924865..51925857-chr19:52140333..52141234,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SIGLEC14-1	chr19:52148730-52148798	ENSG00000258669.1

No data

Variant related genes	Relation type
SIGLEC14	TF binding region
ENSG00000268500	TF binding region
RPL7P51	TF binding region
SIGLEC5	TF binding region
SIGLEC14	CpG island
ENSG00000268500	CpG island
RPL7P51	CpG island
SIGLEC5	CpG island
ENSG00000105366	chromatin interactions
ENSG00000213822	chromatin interactions

Extended variants
information (count: 479 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543717937	chr19:52136203-52136204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189691881	chr19:52136216-52136217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs56193467	chr19:52136273-52136274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575371270	chr19:52136338-52136339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183374237	chr19:52136347-52136348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554355619	chr19:52136433-52136434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145473388	chr19:52136575-52136576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147681404	chr19:52136595-52136596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188705779	chr19:52136609-52136610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs193171893	chr19:52136630-52136631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372437377	chr19:52136651-52136652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142348194	chr19:52136653-52136654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144609798	chr19:52136691-52136692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs151333168	chr19:52136701-52136702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200621992	chr19:52136716-52136717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549269864	chr19:52136727-52136728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183324852	chr19:52136735-52136736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528765541	chr19:52136753-52136754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371379593	chr19:52136777-52136778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547331313	chr19:52136789-52136790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571245812	chr19:52136795-52136796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188284373	chr19:52136808-52136809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140594837	chr19:52136809-52136810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377331728	chr19:52136841-52136842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371087455	chr19:52136844-52136845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191652517	chr19:52136845-52136846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536351874	chr19:52136899-52136900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112036770	chr19:52136930-52136931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572719322	chr19:52136931-52136932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551070049	chr19:52136942-52136943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547656519	chr19:52136952-52136953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533821365	chr19:52136964-52136965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558453523	chr19:52136986-52136987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570921370	chr19:52137081-52137082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201014502	chr19:52137095-52137096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184139198	chr19:52137106-52137107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186973900	chr19:52137108-52137109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191343736	chr19:52137133-52137134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs202099132	chr19:52137154-52137155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6509559	chr19:52137218-52137219	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs6509560	chr19:52137250-52137251	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs138283594	chr19:52137284-52137285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543128722	chr19:52137285-52137286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561433382	chr19:52137296-52137297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141324199	chr19:52137328-52137329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540904119	chr19:52137357-52137358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6509561	chr19:52137561-52137562	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs185053906	chr19:52137590-52137591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550263411	chr19:52137668-52137669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs80042996	chr19:52137726-52137727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52133800-52136200	Enhancers	Placenta	Placenta
2	chr19:52134200-52140200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr19:52134200-52144400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr19:52134400-52138000	Weak transcription	Primary B cells from cord blood	blood
5	chr19:52134600-52137800	Weak transcription	Primary B cells from peripheral blood	blood
6	chr19:52134600-52139400	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr19:52134600-52139400	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr19:52135200-52140000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr19:52137800-52141200	Enhancers	Primary B cells from peripheral blood	blood
10	chr19:52138000-52140600	Enhancers	Primary B cells from cord blood	blood
11	chr19:52139400-52141200	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr19:52139400-52141400	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr19:52139600-52140800	Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr19:52140000-52140200	Enhancers	Placenta Amnion	Placenta Amnion
15	chr19:52140200-52140600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr19:52141200-52142400	Weak transcription	Primary B cells from peripheral blood	blood
17	chr19:52141200-52142600	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr19:52141400-52142200	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr19:52142200-52143600	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr19:52142400-52143600	Strong transcription	Primary B cells from peripheral blood	blood
21	chr19:52142600-52144000	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr19:52143600-52147800	Genic enhancers	Primary monocytes fromperipheralblood	blood
23	chr19:52143600-52147800	Genic enhancers	Primary B cells from peripheral blood	blood
24	chr19:52144000-52144200	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr19:52144200-52145400	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr19:52144400-52144600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
27	chr19:52144600-52146400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr19:52144600-52146800	Weak transcription	Spleen	Spleen
29	chr19:52145400-52145600	Genic enhancers	Monocytes-CD14+_RO01746	blood
30	chr19:52145400-52148000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr19:52145600-52147800	Enhancers	Primary B cells from cord blood	blood
32	chr19:52145600-52147800	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
33	chr19:52146400-52147200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr19:52146400-52147800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr19:52146400-52148400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr19:52146800-52147200	Weak transcription	Lung	lung
37	chr19:52146800-52147800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr19:52146800-52148000	Genic enhancers	Spleen	Spleen
39	chr19:52146800-52150200	Active TSS	Primary neutrophils fromperipheralblood	blood
40	chr19:52147200-52147400	Enhancers	Lung	lung
41	chr19:52147200-52148200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr19:52147200-52153400	Weak transcription	Right Atrium	heart
43	chr19:52147400-52147600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
44	chr19:52147400-52149200	Enhancers	GM12878-XiMat	blood
45	chr19:52147600-52147800	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
46	chr19:52147600-52147800	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr19:52147600-52148000	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr19:52147800-52148000	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
49	chr19:52147800-52148000	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
50	chr19:52147800-52148200	Transcr. at gene 5' and 3'	Primary monocytes fromperipheralblood	blood

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