Variant report

Variant	nsv603351
Chromosome Location	chr6:63069063-63173293
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	ATF2	chr6:63077568-63077881	GM12878	blood:	n/a	n/a
2	BHLHE40	chr6:63115576-63115579	GM12878	blood:	n/a	n/a
3	CEBPB	chr6:63139603-63139831	HepG2	liver:	n/a	chr6:63139771-63139782
4	CEBPB	chr6:63072299-63072645	HepG2	liver:	n/a	chr6:63072437-63072450 chr6:63072437-63072450 chr6:63072438-63072449 chr6:63072628-63072641
5	CEBPB	chr6:63085265-63085473	HepG2	liver:	n/a	n/a
6	CEBPB	chr6:63137661-63138000	HepG2	liver:	n/a	chr6:63137839-63137850
7	CEBPB	chr6:63137819-63137947	A549	lung:	n/a	chr6:63137839-63137850
8	CEBPB	chr6:63165587-63165869	IMR90	lung:	n/a	n/a
9	CEBPB	chr6:63135857-63136005	K562	blood:	n/a	chr6:63135923-63135932 chr6:63135921-63135934 chr6:63135923-63135932 chr6:63135923-63135932 chr6:63135923-63135932 chr6:63135923-63135934
10	CHD2	chr6:63103731-63103782	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr6:63103620-63103770	Caco-2	colon:	n/a	n/a
12	CTCF	chr6:63119223-63119236	GM10248	blood:	n/a	n/a
13	CTCF	chr6:63103680-63103830	HEK293	kidney:	n/a	n/a
14	CTCF	chr6:63103640-63103790	HepG2	liver:	n/a	n/a
15	CTCF	chr6:63103580-63103730	GM12872	blood:	n/a	n/a
16	CTCF	chr6:63103660-63103810	GM12874	blood:	n/a	n/a
17	CTCF	chr6:63103660-63103810	GM12866	blood:	n/a	n/a
18	CTCF	chr6:63103760-63103910	GM12872	blood:	n/a	n/a
19	CTCF	chr6:63103640-63103790	GM12871	blood:	n/a	n/a
20	CTCF	chr6:63109636-63109687	Medullo	brain:	n/a	n/a
21	CTCF	chr6:63103660-63103810	HepG2	liver:	n/a	n/a
22	CTCF	chr6:63120770-63120842	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr6:63103679-63103802	HepG2	liver:	n/a	n/a
24	CTCF	chr6:63123877-63123967	GM10248	blood:	n/a	n/a
25	CTCF	chr6:63103600-63103750	NB4	blood:	n/a	n/a
26	CTCF	chr6:63159014-63159149	LNCaP	prostate:	n/a	n/a
27	CTCF	chr6:63159012-63159193	GM12878	blood:	n/a	n/a
28	CTCF	chr6:63159000-63159152	LNCaP	prostate:	n/a	n/a
29	CTCF	chr6:63103700-63103850	Caco-2	colon:	n/a	n/a
30	E2F4	chr6:63089400-63089591	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr6:63101519-63101896	MCF10A-Er-Src	breast:	n/a	n/a
32	ELK1	chr6:63077661-63077792	GM12878	blood:	n/a	n/a
33	FOS	chr6:63086652-63086981	MCF10A-Er-Src	breast:	n/a	chr6:63086809-63086817 chr6:63086808-63086818 chr6:63086810-63086817 chr6:63086809-63086818 chr6:63086808-63086817 chr6:63086807-63086819
34	FOS	chr6:63100290-63100843	MCF10A-Er-Src	breast:	n/a	chr6:63100538-63100547 chr6:63100501-63100511 chr6:63100540-63100547 chr6:63100502-63100510
35	FOS	chr6:63100189-63100750	MCF10A-Er-Src	breast:	n/a	chr6:63100538-63100547 chr6:63100501-63100511 chr6:63100540-63100547 chr6:63100502-63100510
36	FOS	chr6:63086670-63086982	MCF10A-Er-Src	breast:	n/a	chr6:63086809-63086817 chr6:63086808-63086818 chr6:63086810-63086817 chr6:63086809-63086818 chr6:63086808-63086817 chr6:63086807-63086819
37	FOS	chr6:63086736-63086936	MCF10A-Er-Src	breast:	n/a	chr6:63086809-63086817 chr6:63086808-63086818 chr6:63086810-63086817 chr6:63086809-63086818 chr6:63086808-63086817 chr6:63086807-63086819
38	FOS	chr6:63086670-63086968	MCF10A-Er-Src	breast:	n/a	chr6:63086809-63086817 chr6:63086808-63086818 chr6:63086810-63086817 chr6:63086809-63086818 chr6:63086808-63086817 chr6:63086807-63086819
39	FOS	chr6:63123380-63123580	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr6:63100309-63100727	MCF10A-Er-Src	breast:	n/a	chr6:63100538-63100547 chr6:63100501-63100511 chr6:63100540-63100547 chr6:63100502-63100510
41	FOS	chr6:63100288-63100751	MCF10A-Er-Src	breast:	n/a	chr6:63100538-63100547 chr6:63100501-63100511 chr6:63100540-63100547 chr6:63100502-63100510
42	FOSL2	chr6:63100344-63100779	MCF-7	breast:	n/a	chr6:63100538-63100547 chr6:63100501-63100511 chr6:63100540-63100547 chr6:63100502-63100510
43	FOXA1	chr6:63156563-63156946	HepG2	liver:	n/a	chr6:63156738-63156753 chr6:63156782-63156794
44	GATA2	chr6:63087866-63088281	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr6:63076369-63076641	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr6:63087830-63088301	SH-SY5Y	brain:	n/a	n/a
47	GTF2F1	chr6:63157554-63157571	K562	blood:	n/a	n/a
48	JUN	chr6:63100427-63100644	HepG2	liver:	n/a	chr6:63100538-63100547 chr6:63100501-63100511 chr6:63100540-63100547 chr6:63100502-63100510
49	JUN	chr6:63086755-63086955	HepG2	liver:	n/a	chr6:63086809-63086817 chr6:63086808-63086818 chr6:63086810-63086817 chr6:63086809-63086818 chr6:63086808-63086817 chr6:63086807-63086819
50	JUN	chr6:63089141-63089395	HepG2	liver:	n/a	chr6:63089240-63089253

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:63157784-63157834	HL-60	blood:	n/a
2	chr6:63157784-63157834	NHDF-neo	bronchial:	n/a
3	chr6:63157784-63157834	ProgFib	skin:	n/a
4	chr6:63157784-63157834	GM06990	blood:	n/a
5	chr6:63157784-63157834	HEK293	kidney:	embryo
6	chr6:63157784-63157834	HAEpiC	amniotic membrane:	n/a
7	chr6:63157784-63157834	AG09309	skin:	n/a
8	chr6:63157784-63157834	HMEC	breast:	n/a
9	chr6:63157784-63157834	GM19239	blood:	n/a
10	chr6:63157784-63157834	HNPCEpiC	eye:	n/a
11	chr6:63157784-63157834	RPTEC	kidney:	n/a
12	chr6:63157784-63157834	AG10803	skin:	n/a
13	chr6:63157784-63157834	SK-N-SH_RA	brain:	n/a
14	chr6:63157784-63157834	NB4	blood:	n/a
15	chr6:63157784-63157834	PFSK-1	brain:	n/a
16	chr6:63157784-63157834	HCT-116	colon:	n/a
17	chr6:63157784-63157834	NHBE	bronchial:	n/a
18	chr6:63157784-63157834	IMR90	lung:	fetal
19	chr6:63157784-63157834	AG09319	gingival:	n/a
20	chr6:63157784-63157834	K562	blood:	n/a
21	chr6:63157784-63157834	HCM	heart:	n/a
22	chr6:63157784-63157834	SK-N-SH	brain:	n/a
23	chr6:63157784-63157834	HEEpiC	esophagus:	n/a
24	chr6:63157784-63157834	SKMC	muscle:	n/a
25	chr6:63157784-63157834	A549	lung:	n/a
26	chr6:63157784-63157834	MCF10A-Er-Src	breast:	n/a
27	chr6:63157784-63157834	SK-N-MC	brain:	n/a
28	chr6:63157784-63157834	H1-hESC	embryonic stem cell:	embryo
29	chr6:63157784-63157834	BJ	skin:	n/a
30	chr6:63157784-63157834	LNCaP	prostate:	n/a
31	chr6:63157784-63157834	PrEC	prostate:	n/a
32	chr6:63157784-63157834	NT2-D1	testis:	n/a
33	chr6:63157784-63157834	GM12892	blood:	n/a
34	chr6:63157784-63157834	CMK	blood:	n/a
35	chr6:63157784-63157834	AG04450	lung:	fetal
36	chr6:63157784-63157834	BE2_C	brain:	n/a
37	chr6:63157784-63157834	GM12891	blood:	n/a
38	chr6:63157784-63157834	HCF	heart:	n/a
39	chr6:63157784-63157834	HepG2	liver:	n/a
40	chr6:63157784-63157834	NH-A	brain:	n/a
41	chr6:63157784-63157834	ECC-1	luminal epithelium:	n/a
42	chr6:63157784-63157834	Hela-S3	cervix:	n/a
43	chr6:63157784-63157834	Jurkat	blood:	n/a
44	chr6:63157784-63157834	HRE	kidney:	n/a
45	chr6:63157784-63157834	Caco-2	colon:	n/a
46	chr6:63157784-63157834	GM12878	blood:	n/a
47	chr6:63157784-63157834	Hepatocyte	liver:	n/a
48	chr6:63157784-63157834	T-47D	breast:	n/a
49	chr6:63157784-63157834	HUVEC	blood vessel:	n/a
50	chr6:63157784-63157834	MCF-7	breast:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KHDRBS2-2	chr6:63170845-63171408	NONHSAT113333

Variant related genes	Relation type
ENSG00000216859	TF binding region
ENSG00000216859	CpG island

Extended variants
information (count: 1788 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1788 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2814651	chr6:63069063-63069064	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539750442	chr6:63069099-63069100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558405241	chr6:63069107-63069108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201475631	chr6:63069166-63069167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73479284	chr6:63069169-63069170	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs370390149	chr6:63069193-63069194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77869718	chr6:63069197-63069198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183866624	chr6:63069211-63069212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188809212	chr6:63069235-63069236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191939371	chr6:63069282-63069283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568260908	chr6:63069285-63069286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs80120955	chr6:63069391-63069392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547148497	chr6:63069401-63069402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78590687	chr6:63069428-63069429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562545447	chr6:63069433-63069434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533120363	chr6:63069479-63069480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527624701	chr6:63069504-63069505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375622971	chr6:63069568-63069569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114139296	chr6:63069583-63069584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74499747	chr6:63069615-63069616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184408558	chr6:63069629-63069630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547014292	chr6:63069701-63069702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139437636	chr6:63069759-63069760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2639414	chr6:63069828-63069829	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs539264475	chr6:63069833-63069834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368807865	chr6:63069861-63069862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372132787	chr6:63069869-63069870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186919117	chr6:63069877-63069878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551812104	chr6:63069878-63069879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143390375	chr6:63069885-63069886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35295367	chr6:63069931-63069932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111486211	chr6:63069939-63069940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2842809	chr6:63069946-63069947	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs117277335	chr6:63069957-63069958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547234126	chr6:63069960-63069961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532160803	chr6:63069987-63069988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556189645	chr6:63070013-63070014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191816160	chr6:63070060-63070061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184299414	chr6:63070118-63070119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2265913	chr6:63070151-63070152	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs189632642	chr6:63070152-63070153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371924124	chr6:63070172-63070173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562069117	chr6:63070210-63070211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs80095950	chr6:63070240-63070241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534420443	chr6:63070264-63070265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550814084	chr6:63070268-63070269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9364087	chr6:63070272-63070273	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs35041334	chr6:63070290-63070291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570313704	chr6:63070296-63070297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77615021	chr6:63070297-63070298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	CNVD
Lung cancer	19547694	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Schizophrenia	23813976	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:63066600-63081600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:63068400-63076400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:63068800-63076600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:63076200-63077600	Enhancers	Primary hematopoietic stem cells	blood
5	chr6:63076200-63077800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr6:63076400-63077000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:63076400-63077600	Enhancers	Primary B cells from cord blood	blood
8	chr6:63076400-63078400	Enhancers	Primary B cells from peripheral blood	blood
9	chr6:63076600-63079000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:63077000-63078400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr6:63077600-63078000	Flanking Active TSS	Primary B cells from cord blood	blood
12	chr6:63077600-63078000	Flanking Active TSS	Primary hematopoietic stem cells	blood
13	chr6:63077600-63078000	Active TSS	Monocytes-CD14+_RO01746	blood
14	chr6:63077800-63078200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
15	chr6:63078000-63078800	Enhancers	Primary B cells from cord blood	blood
16	chr6:63078000-63079200	Enhancers	Primary hematopoietic stem cells	blood
17	chr6:63078200-63079000	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr6:63078400-63078600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr6:63078600-63081400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:63079000-63083400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr6:63079200-63079600	Weak transcription	Primary hematopoietic stem cells	blood
22	chr6:63079600-63080000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
23	chr6:63080000-63081800	Weak transcription	Primary hematopoietic stem cells	blood
24	chr6:63081200-63082000	Enhancers	Primary B cells from peripheral blood	blood
25	chr6:63081200-63082000	Enhancers	Fetal Brain Male	brain
26	chr6:63081200-63083400	Enhancers	Primary B cells from cord blood	blood
27	chr6:63081400-63081600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:63081400-63082000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr6:63081400-63082000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:63081400-63082800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:63081400-63084000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:63081600-63081800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:63081600-63081800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:63081600-63082000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr6:63081600-63082000	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr6:63081800-63082000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr6:63081800-63082200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr6:63081800-63082200	Enhancers	Primary hematopoietic stem cells	blood
39	chr6:63082000-63082400	Weak transcription	Fetal Brain Male	brain
40	chr6:63082000-63083200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr6:63082000-63083600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:63082200-63083400	Weak transcription	Primary hematopoietic stem cells	blood
43	chr6:63082400-63082800	Enhancers	Fetal Brain Male	brain
44	chr6:63083200-63083800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr6:63083400-63083800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr6:63083600-63083800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr6:63083600-63083800	Enhancers	Primary B cells from peripheral blood	blood
48	chr6:63083600-63083800	Enhancers	Primary hematopoietic stem cells	blood
49	chr6:63083600-63083800	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr6:63083800-63086600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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