Variant report

Variant	nsv578949
Chromosome Location	chr19:21190572-21244049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:927)
CpG islands
(count:490)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:927 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21203103-21203905	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:21203172-21203518	K562	blood:	n/a	n/a
3	ATF1	chr19:21203206-21203570	K562	blood:	n/a	n/a
4	ATF2	chr19:21211128-21211612	GM12878	blood:	n/a	n/a
5	ATF2	chr19:21203137-21203776	GM12878	blood:	n/a	n/a
6	ATF2	chr19:21205758-21206247	GM12878	blood:	n/a	n/a
7	ATF2	chr19:21211069-21211600	GM12878	blood:	n/a	n/a
8	ATF3	chr19:21205907-21206172	K562	blood:	n/a	n/a
9	BACH1	chr19:21203736-21203976	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr19:21203338-21203360	K562	blood:	n/a	n/a
11	BATF	chr19:21211727-21212086	GM12878	blood:	n/a	n/a
12	BATF	chr19:21205876-21206186	GM12878	blood:	n/a	n/a
13	BATF	chr19:21205859-21206209	GM12878	blood:	n/a	n/a
14	BATF	chr19:21211304-21211567	GM12878	blood:	n/a	chr19:21211457-21211467
15	BATF	chr19:21210999-21211662	GM12878	blood:	n/a	chr19:21211457-21211467
16	BCL11A	chr19:21205878-21206151	GM12878	blood:	n/a	n/a
17	BCL11A	chr19:21210944-21211891	GM12878	blood:	n/a	chr19:21211460-21211469 chr19:21211459-21211468
18	BCL11A	chr19:21211293-21211575	GM12878	blood:	n/a	chr19:21211460-21211469 chr19:21211459-21211468
19	BCL11A	chr19:21205905-21206089	GM12878	blood:	n/a	n/a
20	BCL3	chr19:21211314-21211625	GM12878	blood:	n/a	chr19:21211460-21211469 chr19:21211459-21211468
21	BCL3	chr19:21205826-21206186	GM12878	blood:	n/a	n/a
22	BCLAF1	chr19:21211186-21211620	GM12878	blood:	n/a	chr19:21211460-21211469 chr19:21211459-21211468
23	BCLAF1	chr19:21203607-21204001	GM12878	blood:	n/a	n/a
24	BCLAF1	chr19:21203409-21203891	GM12878	blood:	n/a	n/a
25	BHLHE40	chr19:21211136-21211643	GM12878	blood:	n/a	n/a
26	BHLHE40	chr19:21203109-21203898	GM12878	blood:	n/a	n/a
27	BHLHE40	chr19:21203279-21203977	K562	blood:	n/a	n/a
28	BHLHE40	chr19:21205891-21206180	GM12878	blood:	n/a	n/a
29	BHLHE40	chr19:21221243-21221545	GM12878	blood:	n/a	n/a
30	BRCA1	chr19:21203325-21203834	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr19:21203108-21204025	K562	blood:	n/a	n/a
32	CCNT2	chr19:21203366-21203820	K562	blood:	n/a	chr19:21203640-21203649
33	CEBPB	chr19:21220413-21220667	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:21203180-21203905	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr19:21204509-21204628	K562	blood:	n/a	n/a
36	CEBPB	chr19:21220463-21220631	HepG2	liver:	n/a	n/a
37	CEBPB	chr19:21220067-21220100	HepG2	liver:	n/a	n/a
38	CEBPB	chr19:21230806-21230965	HepG2	liver:	n/a	chr19:21230909-21230920
39	CEBPB	chr19:21219798-21220139	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr19:21205788-21206177	IMR90	lung:	n/a	n/a
41	CEBPB	chr19:21205808-21206145	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr19:21211118-21211724	GM12878	blood:	n/a	n/a
43	CEBPB	chr19:21231884-21232060	K562	blood:	n/a	n/a
44	CEBPB	chr19:21235748-21236054	K562	blood:	n/a	n/a
45	CEBPB	chr19:21219937-21220069	K562	blood:	n/a	n/a
46	CEBPB	chr19:21205807-21206338	HCT-116	colon:	n/a	n/a
47	CEBPB	chr19:21203584-21203778	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr19:21220535-21220616	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr19:21235801-21235931	K562	blood:	n/a	n/a
50	CEBPB	chr19:21205930-21206254	Hela-S3	cervix:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21203493-21203543	HCF	heart:	n/a
2	chr19:21203723-21203773	HRE	kidney:	n/a
3	chr19:21203493-21203543	HCF	heart:	n/a
4	chr19:21203723-21203773	HRE	kidney:	n/a
5	chr19:21203469-21203519	HCT-116	colon:	n/a
6	chr19:21203417-21203467	GM19239	blood:	n/a
7	chr19:21203417-21203467	ECC-1	luminal epithelium:	n/a
8	chr19:21240978-21241028	HCT-116	colon:	n/a
9	chr19:21203417-21203467	Jurkat	blood:	n/a
10	chr19:21203723-21203773	T-47D	breast:	n/a
11	chr19:21240978-21241028	BE2_C	brain:	n/a
12	chr19:21203417-21203467	HCPEpiC	choroid plexus:	n/a
13	chr19:21240978-21241028	ECC-1	luminal epithelium:	n/a
14	chr19:21203444-21203494	NHBE	bronchial:	n/a
15	chr19:21203469-21203519	IMR90	lung:	fetal
16	chr19:21203444-21203494	RPTEC	kidney:	n/a
17	chr19:21203444-21203494	HPAEpiC	pulmonary alveolar:	n/a
18	chr19:21203359-21203409	AG10803	skin:	n/a
19	chr19:21203469-21203519	AG04449	skin:	fetal
20	chr19:21203493-21203543	GM12878	blood:	n/a
21	chr19:21203469-21203519	SK-N-SH_RA	brain:	n/a
22	chr19:21240978-21241028	NH-A	brain:	n/a
23	chr19:21240978-21241028	HMEC	breast:	n/a
24	chr19:21240978-21241028	AG09309	skin:	n/a
25	chr19:21203403-21203453	GM12891	blood:	n/a
26	chr19:21240978-21241028	Jurkat	blood:	n/a
27	chr19:21203723-21203773	MCF10A-Er-Src	breast:	n/a
28	chr19:21203417-21203467	NH-A	brain:	n/a
29	chr19:21203403-21203453	MCF10A-Er-Src	breast:	n/a
30	chr19:21203469-21203519	AG09309	skin:	n/a
31	chr19:21203493-21203543	AG10803	skin:	n/a
32	chr19:21203493-21203543	GM12892	blood:	n/a
33	chr19:21203403-21203453	NHBE	bronchial:	n/a
34	chr19:21203469-21203519	Caco-2	colon:	n/a
35	chr19:21203417-21203467	PANC-1	pancreas:	n/a
36	chr19:21203403-21203453	MCF-7	breast:	n/a
37	chr19:21203723-21203773	HL-60	blood:	n/a
38	chr19:21203359-21203409	NHDF-neo	bronchial:	n/a
39	chr19:21203493-21203543	HRPEpiC	eye:	n/a
40	chr19:21203723-21203773	NB4	blood:	n/a
41	chr19:21203403-21203453	HEK293	kidney:	embryo
42	chr19:21203493-21203543	NB4	blood:	n/a
43	chr19:21203417-21203467	HL-60	blood:	n/a
44	chr19:21203359-21203409	AG09319	gingival:	n/a
45	chr19:21240978-21241028	ProgFib	skin:	n/a
46	chr19:21203469-21203519	HCPEpiC	choroid plexus:	n/a
47	chr19:21203359-21203409	BE2_C	brain:	n/a
48	chr19:21240978-21241028	NT2-D1	testis:	n/a
49	chr19:21203417-21203467	Hepatocyte	liver:	n/a
50	chr19:21203444-21203494	HCT-116	colon:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:21215243..21217384-chr19:21265595..21267237,2	K562	blood:
2	chr19:21203226..21204874-chr19:21207837..21209473,2	MCF-7	breast:
3	chr19:21217901..21220893-chr19:21222403..21225000,3	K562	blood:
4	chr19:21238270..21239771-chr19:21264302..21266943,2	K562	blood:
5	chr17:41398648..41400647-chr19:21234769..21236289,5	MCF-7	breast:
6	chr19:21203269..21205162-chr19:21263863..21266449,2	MCF-7	breast:
7	chr19:21086946..21088802-chr19:21210415..21213328,2	MCF-7	breast:
8	chr19:21230722..21233642-chr19:21264436..21267129,2	K562	blood:
9	chr19:21203226..21204874-chr19:21207837..21209473,2	MCF-7	breast:
10	chr17:41381905..41383742-chr19:21236269..21237789,3	K562	blood:
11	chr19:21236568..21238876-chr19:21241377..21243478,2	K562	blood:
12	chr19:21214855..21215355-chr5:68664827..68665328,2	NB4	blood:
13	chr19:21204714..21207211-chr19:21209787..21213344,3	K562	blood:
14	chr19:21204714..21207211-chr19:21209787..21213344,3	K562	blood:
15	chr19:21217901..21220893-chr19:21222403..21225000,3	K562	blood:
16	chr17:41381927..41383535-chr19:21236269..21237789,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000271598	TF binding region
ENSG00000265650	TF binding region
VN1R80P	TF binding region
ZNF430	TF binding region
ENSG00000271598	CpG island
ENSG00000265650	CpG island
VN1R80P	CpG island
ZNF430	CpG island
ENSG00000085231	chromatin interactions
ENSG00000152942	chromatin interactions
ENSG00000271598	chromatin interactions
ENSG00000160352	chromatin interactions
ENSG00000118620	chromatin interactions
ENSG00000265650	chromatin interactions
ENSG00000236383	chromatin interactions

Extended variants
information (count: 2087 )
Associated
traits (count: 39 )

Variant overlapped rSNPs/rCNVs (count:2087 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373333754	chr19:21190577-21190578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs12104385	chr19:21190578-21190579	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs185026280	chr19:21190581-21190582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs73926911	chr19:21190586-21190587	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs531214977	chr19:21190595-21190596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138487740	chr19:21190604-21190605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12104387	chr19:21190673-21190674	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs571016134	chr19:21190695-21190696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143907015	chr19:21190698-21190699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116963952	chr19:21190738-21190739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566897587	chr19:21190739-21190740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73542629	chr19:21190742-21190743	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs555779642	chr19:21190825-21190826	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs73012919	chr19:21190892-21190893	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs189558354	chr19:21190910-21190911	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557706803	chr19:21191042-21191043	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577725742	chr19:21191063-21191064	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369053245	chr19:21191169-21191170	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568713327	chr19:21191190-21191191	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537558631	chr19:21191221-21191222	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs367583946	chr19:21191258-21191259	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7258477	chr19:21191283-21191284	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs559788581	chr19:21191287-21191288	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375401353	chr19:21191289-21191290	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528872911	chr19:21191316-21191317	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs180745856	chr19:21191388-21191389	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371323978	chr19:21191415-21191416	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562141833	chr19:21191425-21191426	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186003285	chr19:21191463-21191464	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533715465	chr19:21191472-21191473	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148716976	chr19:21191473-21191474	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189675862	chr19:21191476-21191477	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181426171	chr19:21191487-21191488	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573893240	chr19:21191535-21191536	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185795626	chr19:21191595-21191596	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190602334	chr19:21191601-21191602	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536126920	chr19:21191614-21191615	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561262066	chr19:21191644-21191645	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569224493	chr19:21191676-21191677	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372694094	chr19:21191683-21191684	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141438120	chr19:21191737-21191738	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557985130	chr19:21191775-21191776	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555732914	chr19:21191781-21191782	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577782862	chr19:21191811-21191812	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540004783	chr19:21191873-21191874	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113265940	chr19:21191880-21191881	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553534206	chr19:21191905-21191906	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182952299	chr19:21191907-21191908	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542305829	chr19:21191956-21191957	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111787112	chr19:21191966-21191967	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:39)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:2033 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21183400-21193800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:21183400-21196000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr19:21183800-21190800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr19:21183800-21191000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr19:21183800-21194200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr19:21184000-21191200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr19:21184000-21198000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr19:21184400-21196800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr19:21188600-21192200	Strong transcription	H1 Cell Line	embryonic stem cell
10	chr19:21188600-21192600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr19:21189000-21192200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr19:21189000-21192400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr19:21190200-21190800	Strong transcription	Dnd41	blood
14	chr19:21190200-21192400	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr19:21190800-21195400	Weak transcription	Dnd41	blood
16	chr19:21192200-21194000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr19:21192200-21203000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr19:21192400-21203000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr19:21192400-21203400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr19:21192600-21203000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr19:21202800-21203000	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr19:21202800-21203000	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr19:21202800-21203000	Enhancers	Primary T cells fromperipheralblood	blood
24	chr19:21202800-21203000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr19:21202800-21203000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr19:21202800-21203000	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr19:21202800-21203000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr19:21202800-21203000	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr19:21202800-21203000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr19:21202800-21203000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr19:21202800-21203000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr19:21202800-21203000	Enhancers	Fetal Thymus	thymus
33	chr19:21202800-21203000	Enhancers	Thymus	Thymus
34	chr19:21202800-21203000	Active TSS	Dnd41	blood
35	chr19:21202800-21203200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr19:21202800-21204200	Active TSS	Duodenum Mucosa	Duodenum
37	chr19:21202800-21204400	Active TSS	Brain Angular Gyrus	brain
38	chr19:21202800-21204600	Active TSS	Skeletal Muscle Male	skeletal muscle
39	chr19:21202800-21204800	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr19:21202800-21204800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr19:21202800-21204800	Active TSS	Stomach Smooth Muscle	stomach
42	chr19:21203000-21203400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
43	chr19:21203000-21203400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
44	chr19:21203000-21203400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
45	chr19:21203000-21203400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
46	chr19:21203000-21203400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
47	chr19:21203000-21203400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
48	chr19:21203000-21203400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
49	chr19:21203000-21203400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
50	chr19:21203000-21203400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood

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