Variant report

Variant	nsv898754
Chromosome Location	chr12:9696687-9755578
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:153)
CpG islands
(count:245)
Chromatin interactive
region (count:2)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:153 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:9740655-9741170	K562	blood:	n/a	n/a
2	ARID3A	chr12:9743025-9743373	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:9741257-9741854	HepG2	liver:	n/a	n/a
4	ATF1	chr12:9740572-9740926	K562	blood:	n/a	n/a
5	BACH1	chr12:9740595-9741065	K562	blood:	n/a	n/a
6	BACH1	chr12:9740652-9740897	H1-hESC	embryonic stem cell:	n/a	n/a
7	CCNT2	chr12:9740427-9741071	K562	blood:	n/a	n/a
8	CEBPB	chr12:9699995-9700109	A549	lung:	n/a	n/a
9	CEBPB	chr12:9741394-9741705	HepG2	liver:	n/a	n/a
10	CEBPB	chr12:9728216-9728457	A549	lung:	n/a	n/a
11	CEBPB	chr12:9699973-9700136	IMR90	lung:	n/a	n/a
12	CEBPZ	chr12:9741497-9741533	HepG2	liver:	n/a	n/a
13	CTCF	chr12:9736624-9736653	Pancreas_OC	pancreas:	n/a	n/a
14	CTCF	chr12:9730389-9730511	Spleen_OC	spleen:	n/a	n/a
15	CTCF	chr12:9726760-9726829	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr12:9723279-9723384	GM19238	blood:	n/a	n/a
17	CTCF	chr12:9730398-9730556	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr12:9730978-9731104	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr12:9709315-9709383	LNCaP	prostate:	n/a	n/a
20	CTCF	chr12:9723300-9723450	HA-sp	spinal cord:	n/a	n/a
21	CTCF	chr12:9697887-9697942	GM13977	blood:	n/a	n/a
22	CTCF	chr12:9725642-9725709	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr12:9719543-9719625	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr12:9724378-9724451	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr12:9726197-9726271	GM20000	blood:	n/a	n/a
26	CTCF	chr12:9703380-9703388	Kidney_OC	kidney:	n/a	n/a
27	CUX1	chr12:9740702-9741035	K562	blood:	n/a	n/a
28	EP300	chr12:9741267-9741692	HepG2	liver:	n/a	n/a
29	EP300	chr12:9741265-9741740	HepG2	liver:	n/a	n/a
30	EP300	chr12:9740651-9740980	K562	blood:	n/a	n/a
31	FOSL2	chr12:9741379-9741702	HepG2	liver:	n/a	n/a
32	FOSL2	chr12:9730221-9730698	HepG2	liver:	n/a	n/a
33	FOXA1	chr12:9740610-9741156	HepG2	liver:	n/a	n/a
34	FOXA1	chr12:9730241-9730648	HepG2	liver:	n/a	n/a
35	FOXA1	chr12:9739540-9739988	HepG2	liver:	n/a	n/a
36	FOXA1	chr12:9741189-9741723	HepG2	liver:	n/a	n/a
37	FOXA1	chr12:9739540-9739848	HepG2	liver:	n/a	n/a
38	FOXA1	chr12:9741250-9741688	HepG2	liver:	n/a	n/a
39	FOXA1	chr12:9742943-9743533	HepG2	liver:	n/a	n/a
40	FOXA1	chr12:9742968-9743474	HepG2	liver:	n/a	n/a
41	FOXA1	chr12:9740757-9741017	HepG2	liver:	n/a	n/a
42	FOXA1	chr12:9742900-9743418	HepG2	liver:	n/a	n/a
43	FOXA1	chr12:9741190-9741645	HepG2	liver:	n/a	n/a
44	FOXA1	chr12:9742993-9743414	HepG2	liver:	n/a	n/a
45	FOXA2	chr12:9742652-9743719	HepG2	liver:	n/a	n/a
46	FOXA2	chr12:9753093-9753422	A549	lung:	n/a	n/a
47	FOXA2	chr12:9740801-9741029	HepG2	liver:	n/a	n/a
48	FOXA2	chr12:9753085-9753532	A549	lung:	n/a	n/a
49	FOXA2	chr12:9743034-9743338	HepG2	liver:	n/a	n/a
50	GATA3	chr12:9745463-9746018	SH-SY5Y	brain:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9722091-9722141	HAEpiC	amniotic membrane:	n/a
2	chr12:9722091-9722141	HAEpiC	amniotic membrane:	n/a
3	chr12:9722091-9722141	AG10803	skin:	n/a
4	chr12:9720090-9720140	HPAEpiC	pulmonary alveolar:	n/a
5	chr12:9722091-9722141	HUVEC	blood vessel:	n/a
6	chr12:9720090-9720140	Caco-2	colon:	n/a
7	chr12:9723402-9723452	SK-N-SH_RA	brain:	n/a
8	chr12:9720554-9720604	H1-hESC	embryonic stem cell:	embryo
9	chr12:9723402-9723452	BE2_C	brain:	n/a
10	chr12:9723402-9723452	HCM	heart:	n/a
11	chr12:9720554-9720604	SK-N-SH	brain:	n/a
12	chr12:9720554-9720604	AG04450	lung:	fetal
13	chr12:9722091-9722141	HCT-116	colon:	n/a
14	chr12:9720090-9720140	HRCEpiC	kidney:	n/a
15	chr12:9722091-9722141	HRCEpiC	kidney:	n/a
16	chr12:9720090-9720140	HMEC	breast:	n/a
17	chr12:9720554-9720604	GM12892	blood:	n/a
18	chr12:9723402-9723452	AoSMC	blood vessel:	n/a
19	chr12:9720090-9720140	HCT-116	colon:	n/a
20	chr12:9720554-9720604	LNCaP	prostate:	n/a
21	chr12:9722091-9722141	Jurkat	blood:	n/a
22	chr12:9723402-9723452	GM06990	blood:	n/a
23	chr12:9722091-9722141	AoSMC	blood vessel:	n/a
24	chr12:9722091-9722141	T-47D	breast:	n/a
25	chr12:9720090-9720140	HAEpiC	amniotic membrane:	n/a
26	chr12:9720554-9720604	AoSMC	blood vessel:	n/a
27	chr12:9723402-9723452	SKMC	muscle:	n/a
28	chr12:9723402-9723452	A549	lung:	n/a
29	chr12:9723402-9723452	PrEC	prostate:	n/a
30	chr12:9720554-9720604	HEK293	kidney:	embryo
31	chr12:9723402-9723452	HepG2	liver:	n/a
32	chr12:9723402-9723452	MCF10A-Er-Src	breast:	n/a
33	chr12:9720554-9720604	T-47D	breast:	n/a
34	chr12:9722091-9722141	HIPEpiC	eye:	n/a
35	chr12:9720554-9720604	HCM	heart:	n/a
36	chr12:9723402-9723452	K562	blood:	n/a
37	chr12:9723402-9723452	NT2-D1	testis:	n/a
38	chr12:9720090-9720140	Jurkat	blood:	n/a
39	chr12:9720554-9720604	AG10803	skin:	n/a
40	chr12:9720554-9720604	HEEpiC	esophagus:	n/a
41	chr12:9722091-9722141	IMR90	lung:	fetal
42	chr12:9720554-9720604	GM19239	blood:	n/a
43	chr12:9720090-9720140	AG09309	skin:	n/a
44	chr12:9723402-9723452	BJ	skin:	n/a
45	chr12:9720090-9720140	PFSK-1	brain:	n/a
46	chr12:9722091-9722141	HL-60	blood:	n/a
47	chr12:9720090-9720140	HL-60	blood:	n/a
48	chr12:9720090-9720140	GM12878	blood:	n/a
49	chr12:9723402-9723452	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:9723402-9723452	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:9740551..9742492-chr12:9759137..9760711,2	K562	blood:
2	chr12:9739995..9741756-chr12:9800822..9803051,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC2D-9	chr12:9727443-9727545	NONHSAT026830
2	lnc-CLEC2D-9	chr12:9723357-9723488	NONHSAT026830
3	lnc-CLEC2D-9	chr12:9728239-9728313	NONHSAT026830
4	lnc-CLEC2D-9	chr12:9725599-9725666	NONHSAT026830
5	lnc-CLEC2D-9	chr12:9728714-9728863	NONHSAT026830
6	lnc-CLEC2D-9	chr12:9724057-9724169	NONHSAT026830
7	lnc-CLEC2D-9	chr12:9725984-9726130	NONHSAT026830

No data

Variant related genes	Relation type
ENSG00000266633	TF binding region
ENSG00000214776	TF binding region
ENSG00000266633	CpG island
ENSG00000214776	CpG island
ENSG00000111796	chromatin interactions

Extended variants
information (count: 1485 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1485 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374358253	chr12:9696687-9696688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs377419284	chr12:9696769-9696770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139150428	chr12:9696831-9696832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180749212	chr12:9696875-9696876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186341386	chr12:9696932-9696933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs199636668	chr12:9697012-9697013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200162642	chr12:9697048-9697049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2536877	chr12:9697109-9697110	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
9	rs529627530	chr12:9697116-9697117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368165140	chr12:9697147-9697148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370478265	chr12:9697151-9697152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116906566	chr12:9697208-9697209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189177365	chr12:9697250-9697251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375197012	chr12:9697286-9697287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368193309	chr12:9697293-9697294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10843991	chr12:9697297-9697298	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs186957335	chr12:9697313-9697314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375528263	chr12:9697319-9697320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368574565	chr12:9697353-9697354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371465298	chr12:9697359-9697360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191790914	chr12:9697376-9697377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374918572	chr12:9697378-9697379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183128591	chr12:9697409-9697410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186424200	chr12:9697456-9697457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189931402	chr12:9697459-9697460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182142021	chr12:9697481-9697482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369488287	chr12:9697532-9697533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113257186	chr12:9697545-9697546	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
29	rs144689981	chr12:9697718-9697719	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
30	rs200183367	chr12:9697727-9697728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192695473	chr12:9697733-9697734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145716121	chr12:9697765-9697766	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs148917752	chr12:9697931-9697932	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs200715244	chr12:9697939-9697940	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs184019749	chr12:9697970-9697971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188516100	chr12:9698010-9698011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4763576	chr12:9698023-9698024	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs2374758	chr12:9698031-9698032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148165989	chr12:9698049-9698050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374912138	chr12:9698081-9698082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2639041	chr12:9698090-9698091	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
42	rs369459693	chr12:9698113-9698114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547510032	chr12:9698174-9698175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34158342	chr12:9698175-9698176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs71045266	chr12:9698182-9698183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202189104	chr12:9698237-9698238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs3896492	chr12:9698249-9698250	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs78132576	chr12:9698284-9698285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs3867153	chr12:9698296-9698297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4080532	chr12:9698301-9698302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9664200-9702200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr12:9686000-9703600	Weak transcription	Hela-S3	cervix
3	chr12:9703600-9705600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:9704000-9721800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr12:9705600-9706400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr12:9706400-9735000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:9717000-9717400	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr12:9721200-9722400	Weak transcription	Thymus	Thymus
9	chr12:9721400-9723400	Active TSS	Breast Myoepithelial Primary Cells	Breast
10	chr12:9721800-9722000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr12:9721800-9722200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
12	chr12:9721800-9723000	Active TSS	Right Ventricle	heart
13	chr12:9722000-9723000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr12:9722000-9723000	ZNF genes & repeats	Fetal Thymus	thymus
15	chr12:9722200-9722400	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
16	chr12:9722200-9722800	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr12:9722400-9722600	Active TSS	Fetal Muscle Leg	muscle
18	chr12:9722400-9722800	Active TSS	Sigmoid Colon	Sigmoid Colon
19	chr12:9722400-9723000	Active TSS	Thymus	Thymus
20	chr12:9722600-9723200	Flanking Active TSS	Fetal Muscle Leg	muscle
21	chr12:9723000-9723400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr12:9723400-9750600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:9734400-9763000	Weak transcription	Primary hematopoietic stem cells	blood
24	chr12:9736000-9760200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:9738200-9759600	Weak transcription	Primary T cells from cord blood	blood
26	chr12:9739200-9739400	Enhancers	HepG2	liver
27	chr12:9739400-9740400	Weak transcription	HepG2	liver
28	chr12:9740400-9741600	Enhancers	K562	blood
29	chr12:9740400-9744000	Enhancers	HepG2	liver
30	chr12:9740600-9741000	Enhancers	A549	lung
31	chr12:9741200-9741400	Enhancers	Liver	Liver
32	chr12:9741400-9742000	Weak transcription	Liver	Liver
33	chr12:9742000-9742600	Enhancers	Liver	Liver
34	chr12:9742600-9743600	Weak transcription	Liver	Liver
35	chr12:9743200-9743400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr12:9743400-9745600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr12:9743600-9744000	Enhancers	Liver	Liver
38	chr12:9744600-9748600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr12:9744600-9755800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr12:9745600-9746000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr12:9745600-9755600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr12:9745800-9750000	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr12:9746000-9746200	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
44	chr12:9746000-9760000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr12:9746200-9748800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr12:9746600-9756400	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr12:9748400-9750000	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr12:9748600-9748800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr12:9748600-9749000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr12:9748800-9749200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--

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