Variant report

Variant	nsv966489
Chromosome Location	chr4:26600972-26641744
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:129)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:129 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:26615530-26615691	K562	blood:	n/a	n/a
2	ATF1	chr4:26611101-26611405	K562	blood:	n/a	n/a
3	ATF1	chr4:26624399-26624903	K562	blood:	n/a	n/a
4	ATF3	chr4:26624577-26624976	K562	blood:	n/a	chr4:26624749-26624758
5	ATF3	chr4:26624627-26624875	H1-hESC	embryonic stem cell:	n/a	chr4:26624749-26624758
6	BHLHE40	chr4:26624677-26624979	K562	blood:	n/a	n/a
7	CEBPB	chr4:26624363-26625181	K562	blood:	n/a	chr4:26624761-26624772
8	CEBPB	chr4:26601611-26601811	A549	lung:	n/a	chr4:26601693-26601704
9	CEBPB	chr4:26625666-26625845	IMR90	lung:	n/a	n/a
10	CEBPB	chr4:26621487-26621781	HepG2	liver:	n/a	chr4:26621609-26621620
11	CEBPB	chr4:26625665-26625902	K562	blood:	n/a	n/a
12	CEBPB	chr4:26624483-26624883	HCT-116	colon:	n/a	chr4:26624761-26624772
13	CEBPB	chr4:26624577-26624874	K562	blood:	n/a	chr4:26624761-26624772
14	CEBPB	chr4:26624616-26624938	Hela-S3	cervix:	n/a	chr4:26624761-26624772
15	CEBPB	chr4:26624602-26625024	ECC-1	luminal epithelium:	n/a	chr4:26624761-26624772
16	CEBPB	chr4:26601593-26601798	HepG2	liver:	n/a	chr4:26601693-26601704
17	CEBPB	chr4:26601560-26601820	IMR90	lung:	n/a	chr4:26601693-26601704
18	CEBPB	chr4:26624596-26624940	IMR90	lung:	n/a	chr4:26624761-26624772
19	CEBPB	chr4:26601709-26601742	K562	blood:	n/a	n/a
20	CEBPB	chr4:26624628-26624992	A549	lung:	n/a	chr4:26624761-26624772
21	CEBPB	chr4:26624526-26624996	K562	blood:	n/a	chr4:26624761-26624772
22	CEBPB	chr4:26624611-26624937	HepG2	liver:	n/a	chr4:26624761-26624772
23	CEBPB	chr4:26624633-26624945	H1-hESC	embryonic stem cell:	n/a	chr4:26624761-26624772
24	CEBPB	chr4:26624616-26624915	A549	lung:	n/a	chr4:26624761-26624772
25	CEBPB	chr4:26624561-26624909	ECC-1	luminal epithelium:	n/a	chr4:26624761-26624772
26	CEBPB	chr4:26621427-26621812	IMR90	lung:	n/a	chr4:26621609-26621620
27	CEBPB	chr4:26621456-26621761	Hela-S3	cervix:	n/a	chr4:26621609-26621620
28	CTCF	chr4:26605728-26605803	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr4:26630640-26630790	GM12872	blood:	n/a	n/a
30	CTCF	chr4:26605705-26605818	K562	blood:	n/a	n/a
31	CTCF	chr4:26605737-26605800	MCF-7	breast:	n/a	n/a
32	CUX1	chr4:26625768-26625860	K562	blood:	n/a	n/a
33	CUX1	chr4:26637530-26637787	K562	blood:	n/a	chr4:26637732-26637743 chr4:26637737-26637746 chr4:26637738-26637752
34	CUX1	chr4:26625173-26625410	K562	blood:	n/a	n/a
35	CUX1	chr4:26624411-26624786	K562	blood:	n/a	n/a
36	CUX1	chr4:26627039-26627138	K562	blood:	n/a	n/a
37	E2F4	chr4:26621476-26621809	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr4:26638779-26638979	MCF10A-Er-Src	breast:	n/a	n/a
39	EP300	chr4:26626972-26627088	K562	blood:	n/a	n/a
40	EP300	chr4:26624406-26624965	K562	blood:	n/a	chr4:26624762-26624776 chr4:26624858-26624868 chr4:26624784-26624798
41	EP300	chr4:26625347-26625526	K562	blood:	n/a	chr4:26625350-26625359 chr4:26625441-26625451
42	FOS	chr4:26621402-26621806	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr4:26621403-26621761	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr4:26621396-26621773	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr4:26624725-26624796	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr4:26621401-26621807	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr4:26625715-26625844	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr4:26625763-26625811	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr4:26624673-26624782	MCF10A-Er-Src	breast:	n/a	n/a
50	GATA2	chr4:26625557-26625900	SH-SY5Y	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:26609417-26609467	CMK	blood:	n/a
2	chr4:26609417-26609467	SK-N-SH	brain:	n/a
3	chr4:26609417-26609467	SK-N-SH_RA	brain:	n/a
4	chr4:26609417-26609467	ovcar-3	ovarian:	n/a
5	chr4:26609417-26609467	HEEpiC	esophagus:	n/a
6	chr4:26609417-26609467	HCM	heart:	n/a
7	chr4:26609417-26609467	AG04449	skin:	fetal
8	chr4:26609417-26609467	AG09319	gingival:	n/a
9	chr4:26609417-26609467	NH-A	brain:	n/a
10	chr4:26609417-26609467	GM06990	blood:	n/a
11	chr4:26609417-26609467	HMEC	breast:	n/a
12	chr4:26609417-26609467	AoSMC	blood vessel:	n/a
13	chr4:26609417-26609467	A549	lung:	n/a
14	chr4:26609417-26609467	HNPCEpiC	eye:	n/a
15	chr4:26609417-26609467	HCT-116	colon:	n/a
16	chr4:26609417-26609467	Hepatocyte	liver:	n/a
17	chr4:26609417-26609467	T-47D	breast:	n/a
18	chr4:26609417-26609467	RPTEC	kidney:	n/a
19	chr4:26609417-26609467	IMR90	lung:	fetal
20	chr4:26609417-26609467	GM19239	blood:	n/a
21	chr4:26609417-26609467	HRE	kidney:	n/a
22	chr4:26609417-26609467	GM12878	blood:	n/a
23	chr4:26609417-26609467	Hela-S3	cervix:	n/a
24	chr4:26609417-26609467	HCF	heart:	n/a
25	chr4:26609417-26609467	SK-N-MC	brain:	n/a
26	chr4:26609417-26609467	SKMC	muscle:	n/a
27	chr4:26609417-26609467	AG10803	skin:	n/a
28	chr4:26609417-26609467	PANC-1	pancreas:	n/a
29	chr4:26609417-26609467	HAEpiC	amniotic membrane:	n/a
30	chr4:26609417-26609467	LNCaP	prostate:	n/a
31	chr4:26609417-26609467	MCF-7	breast:	n/a
32	chr4:26609417-26609467	MCF10A-Er-Src	breast:	n/a
33	chr4:26609417-26609467	ECC-1	luminal epithelium:	n/a
34	chr4:26609417-26609467	AG09309	skin:	n/a
35	chr4:26609417-26609467	HRPEpiC	eye:	n/a
36	chr4:26609417-26609467	U87	brain:	n/a
37	chr4:26609417-26609467	HepG2	liver:	n/a
38	chr4:26609417-26609467	Jurkat	blood:	n/a
39	chr4:26609417-26609467	HL-60	blood:	n/a
40	chr4:26609417-26609467	HRCEpiC	kidney:	n/a
41	chr4:26609417-26609467	ProgFib	skin:	n/a
42	chr4:26609417-26609467	K562	blood:	n/a
43	chr4:26609417-26609467	BJ	skin:	n/a
44	chr4:26609417-26609467	PrEC	prostate:	n/a
45	chr4:26609417-26609467	NHBE	bronchial:	n/a
46	chr4:26609417-26609467	SAEC	small airway:	n/a
47	chr4:26609417-26609467	PFSK-1	brain:	n/a
48	chr4:26609417-26609467	NHDF-neo	bronchial:	n/a
49	chr4:26609417-26609467	GM12892	blood:	n/a
50	chr4:26609417-26609467	HPAEpiC	pulmonary alveolar:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:26608466..26611373-chr4:26611830..26614579,3	K562	blood:
2	chr4:26625799..26628669-chr4:26629385..26631315,2	K562	blood:
3	chr4:26617271..26620051-chr4:26620097..26621610,2	MCF-7	breast:
4	chr4:26617271..26620051-chr4:26620097..26621610,2	MCF-7	breast:
5	chr4:26608466..26611373-chr4:26611830..26614579,3	K562	blood:
6	chr4:26609663..26611980-chr4:26612126..26613824,2	K562	blood:
7	chr4:26608170..26609762-chr4:26618195..26620999,2	K562	blood:
8	chr4:26609415..26611279-chr4:26625294..26628056,2	K562	blood:
9	chr4:26625799..26628669-chr4:26629385..26631315,2	K562	blood:
10	chr4:26608170..26609762-chr4:26618195..26620999,2	K562	blood:
11	chr4:26609663..26611980-chr4:26612126..26613824,2	K562	blood:
12	chr4:26621660..26623538-chr4:26623814..26625378,2	MCF-7	breast:
13	chr4:26621660..26623538-chr4:26623814..26625378,2	MCF-7	breast:
14	chr4:26609415..26611279-chr4:26625294..26628056,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000265627	TF binding region
ENSG00000265627	CpG island

Extended variants
information (count: 1380 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1380 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561644077	chr4:26600986-26600987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552017870	chr4:26601084-26601085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527608750	chr4:26601090-26601091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183866641	chr4:26601091-26601092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570640958	chr4:26601098-26601099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566432086	chr4:26601113-26601114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565755667	chr4:26601114-26601115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539130789	chr4:26601133-26601134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs17581990	chr4:26601141-26601142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548171518	chr4:26601214-26601215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112631050	chr4:26601305-26601306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535431494	chr4:26601317-26601318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555451313	chr4:26601324-26601325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186294714	chr4:26601330-26601331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563518559	chr4:26601343-26601344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535365104	chr4:26601344-26601345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs62409931	chr4:26601359-26601360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138326148	chr4:26601373-26601374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs578140950	chr4:26601439-26601440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543506562	chr4:26601511-26601512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73114618	chr4:26601561-26601562	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs36092049	chr4:26601597-26601598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373970182	chr4:26601598-26601599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573842531	chr4:26601609-26601610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542588550	chr4:26601652-26601653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559355651	chr4:26601660-26601661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527557228	chr4:26601668-26601669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552259862	chr4:26601699-26601700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190489414	chr4:26601714-26601715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564077037	chr4:26601721-26601722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569156405	chr4:26601730-26601731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533159734	chr4:26601739-26601740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568018236	chr4:26601753-26601754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537756242	chr4:26601758-26601759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569766037	chr4:26601781-26601782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372044863	chr4:26601907-26601908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs117110395	chr4:26601963-26601964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548986691	chr4:26601978-26601979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565697965	chr4:26601982-26601983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534979670	chr4:26601990-26601991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373969696	chr4:26602009-26602010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147314215	chr4:26602058-26602059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs397937986	chr4:26602107-26602108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537643165	chr4:26602164-26602165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534691472	chr4:26602165-26602166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141022316	chr4:26602174-26602175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542727607	chr4:26602222-26602223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571085080	chr4:26602225-26602226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552920860	chr4:26602230-26602231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs149395763	chr4:26602241-26602242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:26586600-26601000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr4:26587000-26602000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr4:26587000-26603200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:26591600-26609400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:26591800-26607800	Weak transcription	Thymus	Thymus
6	chr4:26596200-26621000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr4:26596800-26601000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:26598800-26613400	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr4:26601800-26602400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr4:26602000-26602200	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr4:26603200-26604000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr4:26606200-26606400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr4:26606400-26615400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr4:26606400-26656600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr4:26607600-26610200	Enhancers	Fetal Thymus	thymus
16	chr4:26607600-26615800	Enhancers	Dnd41	blood
17	chr4:26607800-26609800	Enhancers	Thymus	Thymus
18	chr4:26608000-26613000	Weak transcription	HSMM	muscle
19	chr4:26608200-26609000	Enhancers	Colon Smooth Muscle	Colon
20	chr4:26608200-26610000	Enhancers	Rectal Smooth Muscle	rectum
21	chr4:26608400-26609400	Enhancers	NHDF-Ad	bronchial
22	chr4:26608600-26608800	Enhancers	Fetal Heart	heart
23	chr4:26608600-26608800	Enhancers	Fetal Lung	lung
24	chr4:26608600-26608800	Enhancers	Psoas Muscle	Psoas
25	chr4:26608600-26609000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr4:26608800-26609400	Weak transcription	Fetal Lung	lung
27	chr4:26608800-26609400	Weak transcription	Psoas Muscle	Psoas
28	chr4:26608800-26643600	Weak transcription	Fetal Heart	heart
29	chr4:26609000-26609400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:26609000-26625400	Weak transcription	Colon Smooth Muscle	Colon
31	chr4:26609400-26609600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr4:26609400-26609600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr4:26609400-26609600	Enhancers	Fetal Lung	lung
34	chr4:26609400-26609600	Enhancers	Left Ventricle	heart
35	chr4:26609400-26609600	Enhancers	Psoas Muscle	Psoas
36	chr4:26609400-26610000	Enhancers	K562	blood
37	chr4:26609400-26621400	Weak transcription	NHDF-Ad	bronchial
38	chr4:26609600-26610000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chr4:26609600-26610400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr4:26609600-26610400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr4:26609600-26619400	Weak transcription	Fetal Lung	lung
42	chr4:26609600-26621200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr4:26609600-26640000	Weak transcription	Left Ventricle	heart
44	chr4:26609600-26649400	Weak transcription	Psoas Muscle	Psoas
45	chr4:26609800-26610200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr4:26609800-26610400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr4:26609800-26610400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr4:26609800-26611000	Weak transcription	Thymus	Thymus
49	chr4:26609800-26632400	Weak transcription	Primary B cells from cord blood	blood
50	chr4:26610000-26610200	Enhancers	Primary T cells from cord blood	blood

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