Variant report

Variant	nsv875744
Chromosome Location	chr2:208952810-208994045
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:327)
CpG islands
(count:1342)
Chromatin interactive
region (count:13)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:208971322-208971335	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:208989435-208989474	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr2:208966736-208966896	HepG2	liver:	n/a	n/a
4	BHLHE40	chr2:208964451-208964747	HepG2	liver:	n/a	n/a
5	BRCA1	chr2:208977581-208978020	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr2:208977669-208978022	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr2:208955237-208955479	HepG2	liver:	n/a	chr2:208955369-208955380
8	CEBPB	chr2:208955324-208955508	A549	lung:	n/a	chr2:208955369-208955380
9	CEBPB	chr2:208977579-208978082	MCF-7	breast:	n/a	n/a
10	CEBPB	chr2:208955228-208955409	K562	blood:	n/a	chr2:208955369-208955380
11	CEBPB	chr2:208955313-208955467	IMR90	lung:	n/a	chr2:208955369-208955380
12	CEBPB	chr2:208964828-208965044	HepG2	liver:	n/a	chr2:208964913-208964924 chr2:208964925-208964936
13	CEBPB	chr2:208976666-208976729	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:208964877-208965077	A549	lung:	n/a	chr2:208964913-208964924 chr2:208964925-208964936
15	CEBPB	chr2:208984500-208984694	HepG2	liver:	n/a	chr2:208984649-208984660
16	CHD2	chr2:208964047-208964194	HepG2	liver:	n/a	n/a
17	CHD2	chr2:208964017-208964290	K562	blood:	n/a	n/a
18	CTCF	chr2:208966716-208966991	ECC-1	luminal epithelium:	n/a	chr2:208966862-208966875
19	CTCF	chr2:208966740-208966890	AG09309	skin:	n/a	chr2:208966862-208966875
20	CTCF	chr2:208966780-208966930	HPAF	blood vessel:	n/a	chr2:208966862-208966875
21	CTCF	chr2:208953180-208953330	GM12874	blood:	n/a	n/a
22	CTCF	chr2:208966800-208966950	HMEC	breast:	n/a	chr2:208966862-208966875
23	CTCF	chr2:208966780-208966930	AoAF	blood vessel:	n/a	chr2:208966862-208966875
24	CTCF	chr2:208966840-208966990	RPTEC	kidney:	n/a	chr2:208966862-208966875
25	CTCF	chr2:208966779-208966941	GM12878	blood:	n/a	chr2:208966862-208966875
26	CTCF	chr2:208966820-208966970	NB4	blood:	n/a	chr2:208966862-208966875
27	CTCF	chr2:208953240-208953390	HepG2	liver:	n/a	n/a
28	CTCF	chr2:208966739-208966965	LNCaP	prostate:	n/a	chr2:208966862-208966875
29	CTCF	chr2:208966820-208966970	RPTEC	kidney:	n/a	chr2:208966862-208966875
30	CTCF	chr2:208966760-208966910	HVMF	connective:	n/a	chr2:208966862-208966875
31	CTCF	chr2:208966860-208967010	BE2_C	brain:	n/a	chr2:208966862-208966875
32	CTCF	chr2:208966660-208966999	A549	lung:	n/a	chr2:208966862-208966875
33	CTCF	chr2:208966760-208966910	WERI-Rb-1	eye:	n/a	chr2:208966862-208966875
34	CTCF	chr2:208966820-208966970	HFF-Myc	foreskin:	n/a	chr2:208966862-208966875
35	CTCF	chr2:208966800-208966950	AG09309	skin:	n/a	chr2:208966862-208966875
36	CTCF	chr2:208966757-208966978	HUVEC	blood vessel:	n/a	chr2:208966862-208966875
37	CTCF	chr2:208966860-208967010	HRPEpiC	eye:	n/a	chr2:208966862-208966875
38	CTCF	chr2:208966772-208966947	SK-N-SH_RA	brain:	n/a	chr2:208966862-208966875
39	CTCF	chr2:208966740-208966890	K562	blood:	n/a	chr2:208966862-208966875
40	CTCF	chr2:208966780-208966930	HUVEC	blood vessel:	n/a	chr2:208966862-208966875
41	CTCF	chr2:208977340-208977490	HEK293	kidney:	n/a	n/a
42	CTCF	chr2:208966544-208967249	HCT-116	colon:	n/a	chr2:208966862-208966875
43	CTCF	chr2:208966565-208967282	A549	lung:	n/a	chr2:208966862-208966875
44	CTCF	chr2:208966880-208967030	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr2:208966780-208966930	SK-N-SH_RA	brain:	n/a	chr2:208966862-208966875
46	CTCF	chr2:208966780-208966930	AG09319	gingival:	n/a	chr2:208966862-208966875
47	CTCF	chr2:208966815-208966908	GM10248	blood:	n/a	chr2:208966862-208966875
48	CTCF	chr2:208966720-208966870	GM06990	blood:	n/a	n/a
49	CTCF	chr2:208966620-208966770	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr2:208966700-208966850	A549	lung:	n/a	n/a

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:208988453-208988503	PFSK-1	brain:	n/a
2	chr2:208988932-208988982	GM12878	blood:	n/a
3	chr2:208989469-208989519	A549	lung:	n/a
4	chr2:208977452-208977502	BE2_C	brain:	n/a
5	chr2:208988932-208988982	H1-hESC	embryonic stem cell:	embryo
6	chr2:208973097-208973147	HEEpiC	esophagus:	n/a
7	chr2:208989579-208989629	T-47D	breast:	n/a
8	chr2:208990238-208990288	GM12892	blood:	n/a
9	chr2:208989425-208989475	GM12892	blood:	n/a
10	chr2:208973097-208973147	Caco-2	colon:	n/a
11	chr2:208977121-208977171	PANC-1	pancreas:	n/a
12	chr2:208973097-208973147	U87	brain:	n/a
13	chr2:208988967-208989017	HL-60	blood:	n/a
14	chr2:208976933-208976983	AG09319	gingival:	n/a
15	chr2:208990238-208990288	H1-hESC	embryonic stem cell:	embryo
16	chr2:208988967-208989017	AoSMC	blood vessel:	n/a
17	chr2:208989248-208989298	PANC-1	pancreas:	n/a
18	chr2:208976637-208976687	ProgFib	skin:	n/a
19	chr2:208989209-208989259	H1-hESC	embryonic stem cell:	embryo
20	chr2:208986497-208986547	PrEC	prostate:	n/a
21	chr2:208988453-208988503	Hepatocyte	liver:	n/a
22	chr2:208977121-208977171	HCT-116	colon:	n/a
23	chr2:208976637-208976687	ovcar-3	ovarian:	n/a
24	chr2:208986497-208986547	ProgFib	skin:	n/a
25	chr2:208976933-208976983	HEK293	kidney:	embryo
26	chr2:208989831-208989881	AG10803	skin:	n/a
27	chr2:208977452-208977502	MCF10A-Er-Src	breast:	n/a
28	chr2:208988863-208988913	HCPEpiC	choroid plexus:	n/a
29	chr2:208989579-208989629	GM06990	blood:	n/a
30	chr2:208989579-208989629	AG10803	skin:	n/a
31	chr2:208977452-208977502	HNPCEpiC	eye:	n/a
32	chr2:208976933-208976983	IMR90	lung:	fetal
33	chr2:208986497-208986547	SK-N-MC	brain:	n/a
34	chr2:208973097-208973147	AG10803	skin:	n/a
35	chr2:208988453-208988503	AG04449	skin:	fetal
36	chr2:208973097-208973147	AG09319	gingival:	n/a
37	chr2:208989324-208989374	NHDF-neo	bronchial:	n/a
38	chr2:208988967-208989017	GM06990	blood:	n/a
39	chr2:208989324-208989374	Hepatocyte	liver:	n/a
40	chr2:208989324-208989374	SK-N-SH_RA	brain:	n/a
41	chr2:208988863-208988913	HRE	kidney:	n/a
42	chr2:208976933-208976983	SK-N-MC	brain:	n/a
43	chr2:208993094-208993144	AG09319	gingival:	n/a
44	chr2:208989209-208989259	PrEC	prostate:	n/a
45	chr2:208989425-208989475	ovcar-3	ovarian:	n/a
46	chr2:208989324-208989374	HRCEpiC	kidney:	n/a
47	chr2:208993094-208993144	HIPEpiC	eye:	n/a
48	chr2:208988932-208988982	HIPEpiC	eye:	n/a
49	chr2:208977395-208977445	NHBE	bronchial:	n/a
50	chr2:208977395-208977445	SK-N-MC	brain:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:208973001..208975909-chr2:208979754..208981880,3	MCF-7	breast:
2	chr2:208969150..208970998-chr2:208972838..208975738,2	K562	blood:
3	chr2:208966384..208967489-chr2:209118693..209119619,6	MCF-7	breast:
4	chr2:208969150..208970998-chr2:208972838..208975738,2	K562	blood:
5	chr2:208966373..208967393-chr2:209119818..209120821,3	MCF-7	breast:
6	chr2:208958077..208958586-chr6:50919435..50920170,2	MCF-7	breast:
7	chr2:208966420..208967322-chr2:209013248..209014210,3	MCF-7	breast:
8	chr2:208966807..208967387-chr2:209119787..209120319,2	MCF-7	breast:
9	chr2:208966612..208967170-chr2:209013283..209013824,2	MCF-7	breast:
10	chr2:208965617..208968343-chr2:209118826..209120750,2	MCF-7	breast:
11	chr2:208966122..208966972-chr2:209118729..209119251,2	MCF-7	breast:
12	chr2:208989109..208991585-chr2:208994453..208996077,2	K562	blood:
13	chr2:208973001..208975909-chr2:208979754..208981880,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIKFYVE-4	chr2:208983830-208983949	NONHSAT076631
2	lnc-PIKFYVE-4	chr2:208983830-208983949	NONHSAT076630
3	lnc-PIKFYVE-4	chr2:208983853-208983949	NONHSAT076632
4	lnc-PIKFYVE-4	chr2:208993179-208993284	NONHSAT076631

No data

Variant related genes	Relation type
CRYGD	TF binding region
CRYGEP	TF binding region
CRYGD	CpG island
CRYGEP	CpG island
ENSG00000138413	chromatin interactions
ENSG00000163254	chromatin interactions
ENSG00000231908	chromatin interactions

Extended variants
information (count: 1915 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1915 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6758890	chr2:208952810-208952811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577314045	chr2:208952841-208952842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543611728	chr2:208952878-208952879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78602271	chr2:208952932-208952933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574288462	chr2:208952941-208952942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542920708	chr2:208952984-208952985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559977741	chr2:208952989-208952990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187211985	chr2:208953008-208953009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547302228	chr2:208953036-208953037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551792199	chr2:208953181-208953182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6759362	chr2:208953207-208953208	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs143926958	chr2:208953229-208953230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550012059	chr2:208953294-208953295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191085851	chr2:208953295-208953296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4675731	chr2:208953316-208953317	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs376394779	chr2:208953326-208953327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549041559	chr2:208953338-208953339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182927373	chr2:208953345-208953346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs151331363	chr2:208953376-208953377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546913070	chr2:208953388-208953389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs6731047	chr2:208953461-208953462	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs557283132	chr2:208953469-208953470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113562328	chr2:208953505-208953506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571016908	chr2:208953614-208953615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536711110	chr2:208953617-208953618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140585251	chr2:208953644-208953645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569322026	chr2:208953674-208953675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370001893	chr2:208953689-208953690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536615461	chr2:208953807-208953808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529500339	chr2:208953813-208953814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553432803	chr2:208953833-208953834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373412965	chr2:208953840-208953841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573576930	chr2:208953876-208953877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374839041	chr2:208953877-208953878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150298640	chr2:208953878-208953879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187441020	chr2:208953885-208953886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190766925	chr2:208953887-208953888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544351025	chr2:208953928-208953929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561418209	chr2:208953952-208953953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12465847	chr2:208953958-208953959	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs549157628	chr2:208953966-208953967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565838751	chr2:208954003-208954004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528328294	chr2:208954004-208954005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372435870	chr2:208954023-208954024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10932237	chr2:208954055-208954056	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs570879978	chr2:208954082-208954083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554110137	chr2:208954108-208954109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs137904612	chr2:208954109-208954110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112962705	chr2:208954133-208954134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556816703	chr2:208954145-208954146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Cervical cancer	21062161	CNVD
Intracranial aneurysm	16715129	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:402 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:208951600-208957800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr2:208956200-208956400	Enhancers	Fetal Intestine Large	intestine
3	chr2:208956400-208957000	Weak transcription	Fetal Intestine Large	intestine
4	chr2:208956400-208957800	Enhancers	Fetal Stomach	stomach
5	chr2:208956800-208958000	Enhancers	HSMMtube	muscle
6	chr2:208957000-208957800	Enhancers	Fetal Intestine Large	intestine
7	chr2:208957000-208958200	Enhancers	Fetal Heart	heart
8	chr2:208957200-208957800	Enhancers	HepG2	liver
9	chr2:208957200-208961000	Enhancers	Placenta	Placenta
10	chr2:208957800-208958200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr2:208957800-208958600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr2:208958200-208960600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr2:208958200-208960600	Weak transcription	Fetal Heart	heart
14	chr2:208958600-208964800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr2:208960600-208961000	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr2:208960600-208961200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:208960600-208963400	Enhancers	Fetal Heart	heart
18	chr2:208961000-208964600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr2:208961000-208964800	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr2:208961200-208964000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr2:208962000-208962600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:208962200-208962400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr2:208962200-208962400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
24	chr2:208962200-208962600	Enhancers	NH-A	brain
25	chr2:208962200-208962600	Bivalent Enhancer	Osteobl	bone
26	chr2:208962200-208963200	Enhancers	Right Atrium	heart
27	chr2:208962200-208963400	Enhancers	Fetal Muscle Leg	muscle
28	chr2:208962400-208968600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr2:208962600-208963200	Enhancers	HSMMtube	muscle
30	chr2:208962800-208963200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr2:208963200-208965400	Weak transcription	Right Atrium	heart
32	chr2:208964000-208964800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr2:208964400-208964800	Enhancers	Dnd41	blood
34	chr2:208964400-208965000	Enhancers	H9 Cell Line	embryonic stem cell
35	chr2:208964600-208965000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr2:208964600-208965200	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr2:208964600-208965200	Enhancers	HepG2	liver
38	chr2:208964600-208966600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr2:208964600-208967400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr2:208964800-208965000	Flanking Active TSS	Dnd41	blood
41	chr2:208964800-208965200	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr2:208964800-208965600	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr2:208964800-208966600	Enhancers	Primary T cells from cord blood	blood
44	chr2:208964800-208966800	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr2:208964800-208966800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr2:208964800-208967000	Enhancers	Primary hematopoietic stem cells	blood
47	chr2:208964800-208967000	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr2:208965000-208965200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr2:208965000-208965400	Enhancers	Dnd41	blood
50	chr2:208965000-208976600	Weak transcription	H9 Cell Line	embryonic stem cell

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