Variant report

Variant	nsv468628
Chromosome Location	chr1:239774670-239812103
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	BRCA1	chr1:239797470-239797513	Hela-S3	cervix:	n/a	n/a
2	BRCA1	chr1:239807790-239807883	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr1:239779986-239780373	Hela-S3	cervix:	n/a	chr1:239780173-239780182 chr1:239780088-239780101 chr1:239780171-239780182 chr1:239780172-239780183 chr1:239779994-239780006 chr1:239779994-239780007
4	CEBPB	chr1:239779942-239780432	MCF-7	breast:	n/a	chr1:239780173-239780182 chr1:239780088-239780101 chr1:239780171-239780182 chr1:239780172-239780183 chr1:239779960-239779971 chr1:239779994-239780006 chr1:239779994-239780007
5	CEBPB	chr1:239779848-239780403	MCF-7	breast:	n/a	chr1:239780173-239780182 chr1:239780088-239780101 chr1:239780171-239780182 chr1:239780172-239780183 chr1:239779960-239779971 chr1:239779994-239780006 chr1:239779994-239780007
6	CEBPB	chr1:239780047-239780400	A549	lung:	n/a	chr1:239780173-239780182 chr1:239780088-239780101 chr1:239780171-239780182 chr1:239780172-239780183
7	CEBPB	chr1:239780000-239780328	HepG2	liver:	n/a	chr1:239780173-239780182 chr1:239780088-239780101 chr1:239780171-239780182 chr1:239780172-239780183
8	CEBPB	chr1:239780008-239780303	A549	lung:	n/a	chr1:239780173-239780182 chr1:239780088-239780101 chr1:239780171-239780182 chr1:239780172-239780183
9	CTCF	chr1:239806253-239806293	GM10248	blood:	n/a	n/a
10	CTCF	chr1:239807050-239807072	GM20000	blood:	n/a	n/a
11	CTCF	chr1:239776156-239776179	MCF-7	breast:	n/a	n/a
12	CTCF	chr1:239776136-239776156	Lung_OC	lung:	n/a	n/a
13	FOS	chr1:239780005-239780344	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr1:239780001-239780327	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr1:239779976-239780352	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr1:239779995-239780365	MCF10A-Er-Src	breast:	n/a	n/a
17	FOSL2	chr1:239779963-239780353	MCF-7	breast:	n/a	n/a
18	FOSL2	chr1:239779912-239780331	MCF-7	breast:	n/a	n/a
19	FOXA1	chr1:239806601-239806827	HepG2	liver:	n/a	n/a
20	FOXA2	chr1:239792013-239792708	A549	lung:	n/a	n/a
21	FOXA2	chr1:239806641-239807015	A549	lung:	n/a	n/a
22	FOXA2	chr1:239806431-239806961	A549	lung:	n/a	n/a
23	FOXA2	chr1:239792144-239792578	A549	lung:	n/a	n/a
24	GATA3	chr1:239775921-239775926	SH-SY5Y	brain:	n/a	n/a
25	GATA3	chr1:239779853-239780437	MCF-7	breast:	n/a	chr1:239780127-239780143 chr1:239780134-239780141
26	GATA3	chr1:239799813-239799892	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr1:239779853-239780387	SK-N-SH	brain:	n/a	chr1:239780127-239780143 chr1:239780134-239780141
28	GATA3	chr1:239779667-239780588	MCF-7	breast:	n/a	chr1:239780127-239780143 chr1:239779717-239779728 chr1:239780134-239780141
29	GATA3	chr1:239809549-239809683	SH-SY5Y	brain:	n/a	n/a
30	GATA3	chr1:239779973-239780394	SK-N-SH	brain:	n/a	chr1:239780127-239780143 chr1:239780134-239780141
31	MAFK	chr1:239780005-239780240	Hela-S3	cervix:	n/a	n/a
32	MAFK	chr1:239795673-239795843	H1-hESC	embryonic stem cell:	n/a	n/a
33	MAX	chr1:239796775-239797036	H1-hESC	embryonic stem cell:	n/a	n/a
34	MYC	chr1:239776334-239776359	MCF10A-Er-Src	breast:	n/a	n/a
35	MYC	chr1:239780033-239780262	MCF10A-Er-Src	breast:	n/a	n/a
36	NANOG	chr1:239796830-239797069	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr1:239806761-239806812	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr1:239784888-239784945	GM12878	blood:	n/a	n/a
39	POLR2A	chr1:239786128-239786169	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr1:239792432-239792573	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr1:239809654-239809768	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr1:239809488-239809943	H1-neurons	neurons:	n/a	n/a
43	POLR2A	chr1:239795081-239795190	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr1:239803264-239803385	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr1:239778939-239779115	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr1:239806739-239806861	A549	lung:	n/a	n/a
47	POLR2A	chr1:239778184-239778384	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr1:239806717-239806871	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr1:239792680-239792706	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr1:239780031-239780400	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:239792663-239792713	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:239806917-239806967	T-47D	breast:	n/a
3	chr1:239792663-239792713	SKMC	muscle:	n/a
4	chr1:239792663-239792713	HUVEC	blood vessel:	n/a
5	chr1:239806917-239806967	PANC-1	pancreas:	n/a
6	chr1:239792663-239792713	HMEC	breast:	n/a
7	chr1:239792663-239792713	NT2-D1	testis:	n/a
8	chr1:239792663-239792713	H1-hESC	embryonic stem cell:	embryo
9	chr1:239806917-239806967	HCPEpiC	choroid plexus:	n/a
10	chr1:239792663-239792713	RPTEC	kidney:	n/a
11	chr1:239806917-239806967	HMEC	breast:	n/a
12	chr1:239806917-239806967	AoSMC	blood vessel:	n/a
13	chr1:239806917-239806967	HL-60	blood:	n/a
14	chr1:239806917-239806967	HRPEpiC	eye:	n/a
15	chr1:239792663-239792713	MCF-7	breast:	n/a
16	chr1:239806917-239806967	ECC-1	luminal epithelium:	n/a
17	chr1:239792663-239792713	SK-N-SH	brain:	n/a
18	chr1:239792663-239792713	BJ	skin:	n/a
19	chr1:239792663-239792713	PrEC	prostate:	n/a
20	chr1:239806917-239806967	MCF10A-Er-Src	breast:	n/a
21	chr1:239792663-239792713	HCF	heart:	n/a
22	chr1:239792663-239792713	GM12892	blood:	n/a
23	chr1:239792663-239792713	Caco-2	colon:	n/a
24	chr1:239806917-239806967	SK-N-SH_RA	brain:	n/a
25	chr1:239806917-239806967	AG04449	skin:	fetal
26	chr1:239806917-239806967	ProgFib	skin:	n/a
27	chr1:239792663-239792713	GM12891	blood:	n/a
28	chr1:239806917-239806967	ovcar-3	ovarian:	n/a
29	chr1:239792663-239792713	HCT-116	colon:	n/a
30	chr1:239792663-239792713	GM19239	blood:	n/a
31	chr1:239792663-239792713	AG09319	gingival:	n/a
32	chr1:239806917-239806967	NHDF-neo	bronchial:	n/a
33	chr1:239806917-239806967	AG10803	skin:	n/a
34	chr1:239806917-239806967	NH-A	brain:	n/a
35	chr1:239792663-239792713	GM12878	blood:	n/a
36	chr1:239806917-239806967	GM19239	blood:	n/a
37	chr1:239792663-239792713	Jurkat	blood:	n/a
38	chr1:239792663-239792713	HAEpiC	amniotic membrane:	n/a
39	chr1:239806917-239806967	HCF	heart:	n/a
40	chr1:239806917-239806967	SK-N-MC	brain:	n/a
41	chr1:239806917-239806967	PFSK-1	brain:	n/a
42	chr1:239792663-239792713	HCPEpiC	choroid plexus:	n/a
43	chr1:239792663-239792713	AG04449	skin:	fetal
44	chr1:239806917-239806967	HCT-116	colon:	n/a
45	chr1:239792663-239792713	AoSMC	blood vessel:	n/a
46	chr1:239806917-239806967	Caco-2	colon:	n/a
47	chr1:239806917-239806967	GM12891	blood:	n/a
48	chr1:239806917-239806967	MCF-7	breast:	n/a
49	chr1:239792663-239792713	A549	lung:	n/a
50	chr1:239792663-239792713	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:239770818..239772337-chr1:239779962..239782828,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHRM3-1	chr1:239795551-239795576	NONHSAT010476
2	lnc-CHRM3-1	chr1:239795524-239795586	NONHSAT010470

Variant related genes	Relation type
CHRM3	TF binding region
CHRM3	CpG island

Extended variants
information (count: 1466 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1466 , 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	rs6685121	chr1:239774670-239774671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537047704	chr1:239774674-239774675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555098935	chr1:239774708-239774709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377745585	chr1:239774717-239774718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553165273	chr1:239774719-239774720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75352638	chr1:239774726-239774727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574689564	chr1:239774781-239774782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541094471	chr1:239774782-239774783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181807920	chr1:239774783-239774784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546425736	chr1:239774801-239774802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111783625	chr1:239774832-239774833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564789788	chr1:239774834-239774835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574504290	chr1:239774864-239774865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112696509	chr1:239774866-239774867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146705538	chr1:239774877-239774878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561972794	chr1:239774881-239774882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529263791	chr1:239774893-239774894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7367117	chr1:239774894-239774895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs386640992	chr1:239774909-239774910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551500929	chr1:239774910-239774911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551333414	chr1:239774911-239774912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186112590	chr1:239774912-239774913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369400780	chr1:239774914-239774915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549276533	chr1:239774918-239774919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567245109	chr1:239774919-239774920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534602538	chr1:239774920-239774921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112703112	chr1:239774921-239774922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112507592	chr1:239774926-239774927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375697296	chr1:239774928-239774929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149114057	chr1:239774932-239774933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370952517	chr1:239774933-239774934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191730958	chr1:239774943-239774944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563778380	chr1:239774955-239774956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562425973	chr1:239774961-239774962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs61598496	chr1:239774962-239774963	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs541069170	chr1:239774965-239774966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543710869	chr1:239774970-239774971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs59571408	chr1:239774999-239775000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs61836584	chr1:239775001-239775002	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs181334340	chr1:239775003-239775004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551540270	chr1:239775008-239775009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370254757	chr1:239775009-239775010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147267673	chr1:239775011-239775012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377163353	chr1:239775015-239775016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139192170	chr1:239775019-239775020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534587408	chr1:239775072-239775073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533501668	chr1:239775086-239775087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546662627	chr1:239775099-239775100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368181408	chr1:239775111-239775112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6673042	chr1:239775203-239775204	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Liposarcoma	21253554	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
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:239774000-239776000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:239775400-239776000	Enhancers	H9 Cell Line	embryonic stem cell
3	chr1:239775800-239776000	Enhancers	Fetal Muscle Leg	muscle
4	chr1:239775800-239776200	Enhancers	Colon Smooth Muscle	Colon
5	chr1:239775800-239776200	Enhancers	Ovary	ovary
6	chr1:239775800-239776200	Enhancers	Stomach Smooth Muscle	stomach
7	chr1:239775800-239776400	Enhancers	Rectal Smooth Muscle	rectum
8	chr1:239776000-239780800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr1:239776000-239780800	Weak transcription	Fetal Muscle Leg	muscle
10	chr1:239779600-239780400	Enhancers	Hela-S3	cervix
11	chr1:239779600-239781800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:239779800-239781800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:239780800-239781400	Enhancers	H9 Cell Line	embryonic stem cell
14	chr1:239780800-239781600	Enhancers	Primary hematopoietic stem cells	blood
15	chr1:239780800-239781800	Enhancers	Fetal Muscle Leg	muscle
16	chr1:239781000-239781600	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr1:239781200-239781600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:239781200-239781600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr1:239781200-239781600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr1:239781200-239781600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr1:239781200-239781800	Enhancers	H1 Cell Line	embryonic stem cell
22	chr1:239781800-239784000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:239784000-239786600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:239784400-239786400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:239786400-239789000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:239786600-239787400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:239792600-239793200	Active TSS	H1 Cell Line	embryonic stem cell
28	chr1:239792600-239793400	Active TSS	H9 Cell Line	embryonic stem cell
29	chr1:239792600-239793400	Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr1:239792600-239793800	Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr1:239792600-239794000	Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr1:239792600-239794200	Active TSS	HUES6 Cell Line	embryonic stem cell
33	chr1:239792800-239793200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr1:239792800-239793400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr1:239792800-239793600	Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr1:239792800-239794000	Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr1:239792800-239794000	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr1:239793200-239793800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr1:239793200-239796600	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr1:239793200-239797200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr1:239793400-239796600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr1:239793600-239797000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr1:239793800-239794200	Enhancers	Primary T cells from cord blood	blood
44	chr1:239793800-239794400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr1:239794000-239794200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr1:239794000-239794400	Enhancers	Pancreas	Pancrea
47	chr1:239794000-239795400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:239794200-239794600	Weak transcription	Primary T cells from cord blood	blood
49	chr1:239794200-239794800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr1:239794200-239796600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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