Variant report

Variant	esv3434625
Chromosome Location	chr1:179805954-179808043
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	ARID3A	chr1:179807635-179807788	K562	blood:	n/a	n/a
2	CEBPB	chr1:179807699-179807827	A549	lung:	n/a	n/a
3	CEBPB	chr1:179807538-179807916	IMR90	lung:	n/a	n/a
4	CEBPB	chr1:179807571-179808096	MCF-7	breast:	n/a	chr1:179808067-179808078
5	CEBPB	chr1:179807587-179807907	MCF-7	breast:	n/a	n/a
6	CTCF	chr1:179807620-179807770	AG04450	lung:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
7	CTCF	chr1:179807600-179807750	HPAF	blood vessel:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
8	CTCF	chr1:179807680-179807830	MCF-7	breast:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
9	CTCF	chr1:179807633-179807768	K562	blood:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
10	CTCF	chr1:179807640-179807790	K562	blood:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
11	CTCF	chr1:179807620-179807770	BJ	skin:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
12	CTCF	chr1:179807479-179807865	MCF-7	breast:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
13	CTCF	chr1:179807580-179807730	HVMF	connective:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
14	CTCF	chr1:179807640-179807790	HFF	foreskin:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
15	CTCF	chr1:179807660-179807810	HMEC	breast:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
16	CTCF	chr1:179807580-179807730	HA-sp	spinal cord:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
17	CTCF	chr1:179807636-179807755	Hela-S3	cervix:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
18	CTCF	chr1:179807620-179807770	Caco-2	colon:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
19	CTCF	chr1:179807560-179807710	AG10803	skin:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
20	CTCF	chr1:179807200-179807350	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr1:179807640-179807790	NB4	blood:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
22	CTCF	chr1:179807620-179807770	AG10803	skin:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
23	CTCF	chr1:179807620-179807770	AoAF	blood vessel:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
24	CTCF	chr1:179807580-179807730	NHLF	lung:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
25	CTCF	chr1:179807680-179807830	HVMF	connective:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
26	CTCF	chr1:179807640-179807790	HCPEpiC	choroid plexus:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
27	CTCF	chr1:179806784-179806829	MCF-7	breast:	n/a	n/a
28	CTCF	chr1:179807640-179807790	HRPEpiC	eye:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
29	CTCF	chr1:179807580-179807730	HAc	cerebellar:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
30	CTCF	chr1:179807520-179807810	WI-38	lung:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
31	CTCF	chr1:179807640-179807790	HepG2	liver:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
32	CTCF	chr1:179807620-179807770	A549	lung:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
33	CTCF	chr1:179807580-179807730	HCM	heart:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
34	CTCF	chr1:179807120-179807270	HCFaa	heart:	n/a	n/a
35	CTCF	chr1:179807640-179807790	AG04450	lung:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
36	CTCF	chr1:179807562-179807787	K562	blood:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
37	CTCF	chr1:179807640-179807790	HPF	lung:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
38	CTCF	chr1:179807620-179807770	AG09319	gingival:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
39	CTCF	chr1:179807640-179807790	Caco-2	colon:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
40	CTCF	chr1:179807580-179807730	AG04449	skin:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
41	CTCF	chr1:179807680-179807830	NHDF-neo	bronchial:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
42	CTCF	chr1:179807420-179807570	A549	lung:	n/a	n/a
43	CTCF	chr1:179807577-179807819	HUVEC	blood vessel:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
44	CTCF	chr1:179807700-179807850	HAc	cerebellar:	n/a	n/a
45	CTCF	chr1:179807740-179807890	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr1:179807520-179807670	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr1:179807680-179807830	HPF	lung:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
48	CTCF	chr1:179807600-179807750	AG04449	skin:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
49	CTCF	chr1:179807660-179807810	WERI-Rb-1	eye:	n/a	chr1:179807681-179807702 chr1:179807691-179807699
50	CTCF	chr1:179807660-179807810	HEK293	kidney:	n/a	chr1:179807681-179807702 chr1:179807691-179807699

No.	Distal block	Cell Line	Cell type
1	chr1:179799294..179801607-chr1:179806721..179809341,2	MCF-7	breast:
2	chr1:179697636..179699556-chr1:179807746..179810744,2	MCF-7	breast:
3	chr1:179807872..179810257-chr1:179811726..179814159,3	K562	blood:

Variant related genes	Relation type
ENSG00000231966	TF binding region
ENSG00000243062	chromatin interactions

Extended variants
information (count: 99 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535160973	chr1:179805960-179805961	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs548570924	chr1:179805974-179805975	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs568485251	chr1:179805979-179805980	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs537293059	chr1:179805988-179805989	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs556982371	chr1:179806004-179806005	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577107371	chr1:179806012-179806013	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539251780	chr1:179806027-179806028	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553159516	chr1:179806028-179806029	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1299683	chr1:179806049-179806050	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs139487693	chr1:179806050-179806051	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577765178	chr1:179806072-179806073	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538497069	chr1:179806093-179806094	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561299330	chr1:179806105-179806106	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187827736	chr1:179806126-179806127	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs193280251	chr1:179806161-179806162	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563826023	chr1:179806165-179806166	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532870345	chr1:179806213-179806214	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369458744	chr1:179806257-179806258	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11581200	chr1:179806288-179806289	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528571682	chr1:179806292-179806293	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373512031	chr1:179806299-179806300	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145012845	chr1:179806310-179806311	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568421502	chr1:179806320-179806321	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs113575633	chr1:179806326-179806327	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550999297	chr1:179806336-179806337	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570633948	chr1:179806357-179806358	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539755264	chr1:179806364-179806365	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs552857960	chr1:179806367-179806368	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201299236	chr1:179806368-179806369	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558140243	chr1:179806381-179806382	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs199502105	chr1:179806382-179806383	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576396556	chr1:179806390-179806391	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566333568	chr1:179806415-179806416	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543879285	chr1:179806416-179806417	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535138458	chr1:179806434-179806435	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555035948	chr1:179806453-179806454	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565279994	chr1:179806457-179806458	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543785652	chr1:179806492-179806493	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557770466	chr1:179806537-179806538	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147599626	chr1:179806538-179806539	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2777916	chr1:179806544-179806545	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs559641388	chr1:179806557-179806558	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528702265	chr1:179806588-179806589	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542480949	chr1:179806589-179806590	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562158765	chr1:179806617-179806618	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531054430	chr1:179806623-179806624	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149680450	chr1:179806630-179806631	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs74370297	chr1:179806641-179806642	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145573308	chr1:179806645-179806646	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546883215	chr1:179806663-179806664	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179791000-179807200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:179793800-179808800	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr1:179794800-179809200	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr1:179795200-179812400	Weak transcription	Left Ventricle	heart
5	chr1:179795200-179815200	Weak transcription	Ovary	ovary
6	chr1:179795400-179807600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:179795400-179815200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr1:179795600-179834200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr1:179797600-179810000	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr1:179799600-179815200	Weak transcription	Brain Angular Gyrus	brain
11	chr1:179800400-179808800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr1:179800400-179809000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr1:179800400-179815200	Weak transcription	Psoas Muscle	Psoas
14	chr1:179800600-179815200	Weak transcription	Esophagus	oesophagus
15	chr1:179800800-179808800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:179800800-179815200	Weak transcription	Hela-S3	cervix
17	chr1:179801000-179814400	Weak transcription	HMEC	breast
18	chr1:179801000-179815000	Weak transcription	K562	blood
19	chr1:179801200-179808800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr1:179801200-179809400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr1:179801200-179810400	Weak transcription	HSMMtube	muscle
22	chr1:179801200-179815200	Weak transcription	Lung	lung
23	chr1:179801200-179815200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr1:179801200-179815200	Weak transcription	Spleen	Spleen
25	chr1:179801400-179808000	Weak transcription	Pancreas	Pancrea
26	chr1:179801400-179810200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr1:179801400-179810600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr1:179801400-179810600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr1:179801600-179813200	Weak transcription	GM12878-XiMat	blood
30	chr1:179801800-179807200	Weak transcription	Osteobl	bone
31	chr1:179801800-179808600	Weak transcription	Liver	Liver
32	chr1:179801800-179808600	Weak transcription	HSMM	muscle
33	chr1:179801800-179808800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr1:179801800-179813200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr1:179801800-179815200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr1:179801800-179815200	Weak transcription	NHDF-Ad	bronchial
37	chr1:179802200-179815200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr1:179802400-179808600	Weak transcription	Primary T cells from cord blood	blood
39	chr1:179802400-179808600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:179802400-179808800	Weak transcription	Fetal Brain Female	brain
41	chr1:179802400-179813400	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr1:179802400-179815000	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr1:179802400-179815200	Weak transcription	Thymus	Thymus
44	chr1:179802400-179836200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr1:179802600-179808800	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr1:179802600-179808800	Weak transcription	Duodenum Mucosa	Duodenum
47	chr1:179802600-179810800	Weak transcription	Fetal Thymus	thymus
48	chr1:179802600-179814200	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr1:179802600-179815200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr1:179802600-179819800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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