Variant report

Variant	nsv432586
Chromosome Location	chr4:22879831-22995431
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	ARID3A	chr4:22899185-22899471	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:22897036-22897520	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:22971300-22971641	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:22899272-22899454	K562	blood:	n/a	n/a
5	BACH1	chr4:22918677-22918719	K562	blood:	n/a	n/a
6	BATF	chr4:22935474-22935715	GM12878	blood:	n/a	n/a
7	BCL11A	chr4:22885970-22886163	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr4:22935500-22935722	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:22935546-22935707	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:22885743-22886105	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr4:22896975-22897295	HepG2	liver:	n/a	n/a
12	BRCA1	chr4:22899347-22899433	HepG2	liver:	n/a	n/a
13	CCNT2	chr4:22990380-22990846	K562	blood:	n/a	n/a
14	CEBPB	chr4:22924888-22925085	A549	lung:	n/a	chr4:22925064-22925075
15	CEBPB	chr4:22970805-22971583	A549	lung:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
16	CEBPB	chr4:22970806-22971153	A549	lung:	n/a	n/a
17	CEBPB	chr4:22885915-22886185	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr4:22919748-22920078	HepG2	liver:	n/a	chr4:22919913-22919924 chr4:22919915-22919924 chr4:22919913-22919926 chr4:22919914-22919925
19	CEBPB	chr4:22970806-22971591	IMR90	lung:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
20	CEBPB	chr4:22924952-22925152	HepG2	liver:	n/a	chr4:22925064-22925075
21	CEBPB	chr4:22962760-22963052	IMR90	lung:	n/a	chr4:22962918-22962931 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962918-22962931
22	CEBPB	chr4:22971200-22971684	A549	lung:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
23	CEBPB	chr4:22962805-22963050	A549	lung:	n/a	chr4:22962918-22962931 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962918-22962931
24	CEBPB	chr4:22919827-22920036	A549	lung:	n/a	chr4:22919913-22919924 chr4:22919915-22919924 chr4:22919913-22919926 chr4:22919914-22919925
25	CEBPB	chr4:22970866-22971624	HepG2	liver:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
26	CEBPB	chr4:22980955-22981301	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:22970778-22971746	A549	lung:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
28	CEBPB	chr4:22971259-22971582	MCF-7	breast:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
29	CEBPB	chr4:22962790-22963068	K562	blood:	n/a	chr4:22962918-22962931 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962918-22962931
30	CEBPB	chr4:22919828-22920030	IMR90	lung:	n/a	chr4:22919913-22919924 chr4:22919915-22919924 chr4:22919913-22919926 chr4:22919914-22919925
31	CEBPB	chr4:22980980-22981287	IMR90	lung:	n/a	n/a
32	CEBPB	chr4:22980982-22981263	K562	blood:	n/a	n/a
33	CEBPB	chr4:22937900-22938162	HepG2	liver:	n/a	chr4:22938010-22938021
34	CEBPB	chr4:22962748-22963083	HepG2	liver:	n/a	chr4:22962918-22962931 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962918-22962931
35	CEBPB	chr4:22970760-22971748	Hela-S3	cervix:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
36	CEBPB	chr4:22981018-22981257	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr4:22885793-22886098	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr4:22907991-22908003	GM12878	blood:	n/a	n/a
39	CTCF	chr4:22964160-22964310	HEK293	kidney:	n/a	chr4:22964210-22964228 chr4:22964212-22964233
40	CTCF	chr4:22964200-22964350	GM12873	blood:	n/a	chr4:22964210-22964228 chr4:22964212-22964233
41	CTCF	chr4:22899080-22899538	MCF-7	breast:	n/a	chr4:22899320-22899329 chr4:22899320-22899333 chr4:22899318-22899334 chr4:22899319-22899340 chr4:22899317-22899335
42	CTCF	chr4:22898920-22899070	AG04450	lung:	n/a	n/a
43	CTCF	chr4:22964085-22964312	LNCaP	prostate:	n/a	chr4:22964210-22964228 chr4:22964212-22964233
44	CTCF	chr4:22898645-22899592	SK-N-SH	brain:	n/a	chr4:22898703-22898711 chr4:22899320-22899329 chr4:22899320-22899333 chr4:22899318-22899334 chr4:22899319-22899340 chr4:22899317-22899335
45	CTCF	chr4:22964120-22964270	SK-N-SH_RA	brain:	n/a	chr4:22964210-22964228 chr4:22964212-22964233
46	CTCF	chr4:22899220-22899370	GM06990	blood:	n/a	chr4:22899320-22899329 chr4:22899320-22899333 chr4:22899318-22899334 chr4:22899319-22899340 chr4:22899317-22899335
47	CTCF	chr4:22899360-22899510	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr4:22964080-22964230	NHEK	skin:	n/a	chr4:22964210-22964228
49	CTCF	chr4:22899260-22899410	MCF-7	breast:	n/a	chr4:22899320-22899329 chr4:22899320-22899333 chr4:22899318-22899334 chr4:22899319-22899340 chr4:22899317-22899335
50	CTCF	chr4:22899231-22899492	H1-hESC	embryonic stem cell:	n/a	chr4:22899320-22899329 chr4:22899320-22899333 chr4:22899318-22899334 chr4:22899319-22899340 chr4:22899317-22899335

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:22913868-22913918	NHBE	bronchial:	n/a
2	chr4:22913868-22913918	MCF-7	breast:	n/a
3	chr4:22913868-22913918	HPAEpiC	pulmonary alveolar:	n/a
4	chr4:22913868-22913918	HCPEpiC	choroid plexus:	n/a
5	chr4:22913868-22913918	AoSMC	blood vessel:	n/a
6	chr4:22913868-22913918	GM06990	blood:	n/a
7	chr4:22913868-22913918	MCF10A-Er-Src	breast:	n/a
8	chr4:22913868-22913918	NH-A	brain:	n/a
9	chr4:22913868-22913918	Jurkat	blood:	n/a
10	chr4:22913868-22913918	NHDF-neo	bronchial:	n/a
11	chr4:22913868-22913918	AG09309	skin:	n/a
12	chr4:22913868-22913918	AG04450	lung:	fetal
13	chr4:22913868-22913918	RPTEC	kidney:	n/a
14	chr4:22913868-22913918	GM12891	blood:	n/a
15	chr4:22913868-22913918	HIPEpiC	eye:	n/a
16	chr4:22913868-22913918	HCF	heart:	n/a
17	chr4:22913868-22913918	CMK	blood:	n/a
18	chr4:22913868-22913918	SK-N-MC	brain:	n/a
19	chr4:22913868-22913918	HepG2	liver:	n/a
20	chr4:22913868-22913918	ProgFib	skin:	n/a
21	chr4:22913868-22913918	T-47D	breast:	n/a
22	chr4:22913868-22913918	ovcar-3	ovarian:	n/a
23	chr4:22913868-22913918	HEK293	kidney:	embryo
24	chr4:22913868-22913918	Hepatocyte	liver:	n/a
25	chr4:22913868-22913918	HEEpiC	esophagus:	n/a
26	chr4:22913868-22913918	HL-60	blood:	n/a
27	chr4:22913868-22913918	NT2-D1	testis:	n/a
28	chr4:22913868-22913918	PFSK-1	brain:	n/a
29	chr4:22913868-22913918	HCT-116	colon:	n/a
30	chr4:22913868-22913918	NB4	blood:	n/a
31	chr4:22913868-22913918	HCM	heart:	n/a
32	chr4:22913868-22913918	ECC-1	luminal epithelium:	n/a
33	chr4:22913868-22913918	BE2_C	brain:	n/a
34	chr4:22913868-22913918	LNCaP	prostate:	n/a
35	chr4:22913868-22913918	K562	blood:	n/a
36	chr4:22913868-22913918	H1-hESC	embryonic stem cell:	embryo
37	chr4:22913868-22913918	HRPEpiC	eye:	n/a
38	chr4:22913868-22913918	HRCEpiC	kidney:	n/a
39	chr4:22913868-22913918	GM19239	blood:	n/a
40	chr4:22913868-22913918	HUVEC	blood vessel:	n/a
41	chr4:22913868-22913918	GM12878	blood:	n/a
42	chr4:22913868-22913918	A549	lung:	n/a
43	chr4:22913868-22913918	PrEC	prostate:	n/a
44	chr4:22913868-22913918	Caco-2	colon:	n/a
45	chr4:22913868-22913918	HNPCEpiC	eye:	n/a
46	chr4:22913868-22913918	SKMC	muscle:	n/a
47	chr4:22913868-22913918	AG04449	skin:	fetal
48	chr4:22913868-22913918	HAEpiC	amniotic membrane:	n/a
49	chr4:22913868-22913918	SK-N-SH_RA	brain:	n/a
50	chr4:22913868-22913918	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:22938501..22940847-chr4:22943530..22945759,2	K562	blood:
2	chr4:22899142..22899801-chr4:24420786..24421361,2	MCF-7	breast:
3	chr4:22927818..22930601-chr4:22932236..22933827,2	K562	blood:
4	chr4:22875811..22877491-chr4:22882089..22884830,2	K562	blood:
5	chr4:22927818..22930601-chr4:22932236..22933827,2	K562	blood:
6	chr4:22992595..22995283-chr4:22996612..22998977,2	K562	blood:
7	chr4:22938501..22940847-chr4:22943530..22945759,2	K562	blood:

Variant related genes	Relation type
ENSG00000248837	TF binding region
ENSG00000248837	CpG island

Extended variants
information (count: 2048 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2048 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115972232	chr4:22879850-22879851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs16873199	chr4:22879857-22879858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546874642	chr4:22879956-22879957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184744332	chr4:22880000-22880001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200251242	chr4:22880100-22880101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186799801	chr4:22880128-22880129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192502695	chr4:22880141-22880142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372789240	chr4:22880188-22880189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536394495	chr4:22880237-22880238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184430412	chr4:22880259-22880260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374738674	chr4:22880306-22880307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145534443	chr4:22880320-22880321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs367575804	chr4:22880350-22880351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7690402	chr4:22880382-22880383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566145671	chr4:22880436-22880437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535220325	chr4:22880488-22880489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189724194	chr4:22880499-22880500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544984114	chr4:22880598-22880599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575063911	chr4:22880609-22880610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142632295	chr4:22880660-22880661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530903028	chr4:22880669-22880670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138063343	chr4:22880676-22880677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543060935	chr4:22880795-22880796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561234884	chr4:22880876-22880877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146942682	chr4:22880927-22880928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546837805	chr4:22881022-22881023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571551045	chr4:22881089-22881090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539967430	chr4:22881091-22881092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546327357	chr4:22881109-22881110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550592617	chr4:22881113-22881114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201831730	chr4:22881118-22881119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568789342	chr4:22881197-22881198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572193095	chr4:22881215-22881216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs376141958	chr4:22881220-22881221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535881487	chr4:22881221-22881222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144867308	chr4:22881224-22881225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566468348	chr4:22881237-22881238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534870085	chr4:22881244-22881245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144809338	chr4:22881273-22881274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181217447	chr4:22881303-22881304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577904258	chr4:22881318-22881319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545339027	chr4:22881334-22881335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76367714	chr4:22881368-22881369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149060991	chr4:22881390-22881391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542670976	chr4:22881391-22881392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561404163	chr4:22881393-22881394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568530390	chr4:22883268-22883269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537754168	chr4:22883275-22883276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376123210	chr4:22883277-22883278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530325999	chr4:22883302-22883303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:202 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22878600-22880800	Enhancers	Brain Germinal Matrix	brain
2	chr4:22878800-22881200	Weak transcription	Fetal Intestine Small	intestine
3	chr4:22879000-22880200	Weak transcription	Fetal Intestine Large	intestine
4	chr4:22880600-22880800	Enhancers	Fetal Intestine Large	intestine
5	chr4:22881200-22881400	Enhancers	Fetal Intestine Small	intestine
6	chr4:22883200-22883800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:22884000-22887400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:22886800-22887600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
9	chr4:22896400-22899200	Enhancers	HepG2	liver
10	chr4:22896800-22898000	Enhancers	Liver	Liver
11	chr4:22898200-22899000	Enhancers	Fetal Lung	lung
12	chr4:22898600-22899200	Enhancers	Fetal Intestine Small	intestine
13	chr4:22899000-22902400	Weak transcription	Fetal Lung	lung
14	chr4:22899400-22901000	Enhancers	Primary hematopoietic stem cells	blood
15	chr4:22899400-22901200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr4:22900000-22901200	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr4:22900000-22901200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:22900400-22900800	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr4:22901200-22905200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr4:22902200-22903000	Enhancers	Colon Smooth Muscle	Colon
21	chr4:22902400-22903000	Enhancers	Fetal Lung	lung
22	chr4:22902600-22903000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr4:22902800-22903200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:22903000-22903600	Weak transcription	Fetal Lung	lung
25	chr4:22903200-22903400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:22903400-22903800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:22903600-22903800	Enhancers	Fetal Lung	lung
28	chr4:22903600-22904200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr4:22905200-22905800	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr4:22905200-22906000	Enhancers	Fetal Heart	heart
31	chr4:22905800-22906000	Enhancers	Duodenum Mucosa	Duodenum
32	chr4:22906000-22906800	Weak transcription	Duodenum Mucosa	Duodenum
33	chr4:22906400-22908400	Enhancers	Fetal Intestine Small	intestine
34	chr4:22906800-22908200	Enhancers	Duodenum Mucosa	Duodenum
35	chr4:22907200-22907600	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr4:22907200-22908200	Enhancers	Fetal Intestine Large	intestine
37	chr4:22907800-22908200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:22911600-22913000	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr4:22912000-22912400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:22912000-22914200	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr4:22913000-22914000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr4:22913200-22913800	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr4:22913200-22914200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:22913400-22914000	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr4:22913400-22914200	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr4:22913600-22914200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr4:22914000-22914200	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr4:22914200-22915200	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr4:22914200-22916200	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr4:22915200-22915600	Enhancers	Primary monocytes fromperipheralblood	blood

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