Variant report

Variant	esv1812374
Chromosome Location	chr3:140544609-140589032
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	chr3:140582604-140582919	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:140547536-140547736	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:140582617-140582913	K562	blood:	n/a	n/a
4	ATF2	chr3:140564672-140565199	GM12878	blood:	n/a	n/a
5	ATF2	chr3:140562011-140562511	GM12878	blood:	n/a	n/a
6	BACH1	chr3:140582646-140582715	K562	blood:	n/a	n/a
7	BACH1	chr3:140569657-140569675	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr3:140562108-140562470	GM12878	blood:	n/a	n/a
9	BCL11A	chr3:140562021-140562506	GM12878	blood:	n/a	chr3:140562252-140562261
10	BCL11A	chr3:140562101-140562449	GM12878	blood:	n/a	chr3:140562252-140562261
11	BHLHE40	chr3:140582520-140582700	K562	blood:	n/a	n/a
12	BHLHE40	chr3:140562193-140562481	GM12878	blood:	n/a	n/a
13	CEBPB	chr3:140578494-140578848	MCF-7	breast:	n/a	n/a
14	CEBPB	chr3:140578468-140578888	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr3:140584271-140584303	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:140557280-140557476	K562	blood:	n/a	n/a
17	CEBPB	chr3:140545802-140545921	K562	blood:	n/a	chr3:140545861-140545874 chr3:140545861-140545874 chr3:140545901-140545912 chr3:140545863-140545874 chr3:140545863-140545874
18	CEBPB	chr3:140578609-140578838	HepG2	liver:	n/a	n/a
19	CEBPB	chr3:140578527-140578835	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:140578527-140578802	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr3:140553895-140554122	HepG2	liver:	n/a	chr3:140554021-140554032
22	CEBPB	chr3:140553951-140554229	MCF-7	breast:	n/a	chr3:140554021-140554032
23	CHD2	chr3:140561955-140562475	GM12878	blood:	n/a	n/a
24	CTCF	chr3:140562195-140562368	GM12878	blood:	n/a	n/a
25	CTCF	chr3:140582635-140582803	HepG2	liver:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
26	CTCF	chr3:140582629-140582803	NHEK	skin:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
27	CTCF	chr3:140582700-140582850	HA-sp	spinal cord:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
28	CTCF	chr3:140582624-140582859	A549	lung:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
29	CTCF	chr3:140567643-140567792	GM19238	blood:	n/a	n/a
30	CTCF	chr3:140583034-140583072	Medullo	brain:	n/a	n/a
31	CTCF	chr3:140567665-140567771	GM19239	blood:	n/a	n/a
32	CTCF	chr3:140567700-140567850	GM06990	blood:	n/a	n/a
33	CTCF	chr3:140582489-140582856	A549	lung:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
34	CTCF	chr3:140567631-140567812	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:140583017-140583079	GM12878	blood:	n/a	n/a
36	CTCF	chr3:140582640-140582790	BJ	skin:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
37	CTCF	chr3:140582920-140583170	NHEK	skin:	n/a	n/a
38	CTCF	chr3:140582300-140582450	AG04449	skin:	n/a	n/a
39	CTCF	chr3:140582648-140582798	MCF-7	breast:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
40	CTCF	chr3:140582683-140582827	GM13976	blood:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
41	CTCF	chr3:140582420-140582570	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr3:140582442-140582922	K562	blood:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
43	CTCF	chr3:140582700-140582850	AG09319	gingival:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
44	CTCF	chr3:140582640-140582790	HCFaa	heart:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
45	CTCF	chr3:140582640-140582790	A549	lung:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
46	CTCF	chr3:140582620-140582770	GM12864	blood:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
47	CTCF	chr3:140582660-140582810	NHDF-neo	bronchial:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
48	CTCF	chr3:140567680-140567830	GM12865	blood:	n/a	n/a
49	CTCF	chr3:140582680-140582830	HVMF	connective:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
50	CTCF	chr3:140582604-140582805	GM19240	blood:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140578726-140578776	HIPEpiC	eye:	n/a
2	chr3:140578726-140578776	GM06990	blood:	n/a
3	chr3:140587268-140587318	NHBE	bronchial:	n/a
4	chr3:140578726-140578776	HEEpiC	esophagus:	n/a
5	chr3:140578726-140578776	Caco-2	colon:	n/a
6	chr3:140587268-140587318	AG09309	skin:	n/a
7	chr3:140587268-140587318	CMK	blood:	n/a
8	chr3:140587268-140587318	HIPEpiC	eye:	n/a
9	chr3:140578726-140578776	BE2_C	brain:	n/a
10	chr3:140578726-140578776	H1-hESC	embryonic stem cell:	embryo
11	chr3:140587268-140587318	HL-60	blood:	n/a
12	chr3:140578726-140578776	RPTEC	kidney:	n/a
13	chr3:140578726-140578776	HCT-116	colon:	n/a
14	chr3:140578726-140578776	GM19239	blood:	n/a
15	chr3:140578726-140578776	SKMC	muscle:	n/a
16	chr3:140578726-140578776	HUVEC	blood vessel:	n/a
17	chr3:140578726-140578776	MCF-7	breast:	n/a
18	chr3:140587268-140587318	HEK293	kidney:	embryo
19	chr3:140587268-140587318	HCPEpiC	choroid plexus:	n/a
20	chr3:140587268-140587318	HepG2	liver:	n/a
21	chr3:140587268-140587318	HNPCEpiC	eye:	n/a
22	chr3:140587268-140587318	HUVEC	blood vessel:	n/a
23	chr3:140578726-140578776	BJ	skin:	n/a
24	chr3:140587268-140587318	AG04450	lung:	fetal
25	chr3:140587268-140587318	Caco-2	colon:	n/a
26	chr3:140578726-140578776	GM12878	blood:	n/a
27	chr3:140578726-140578776	HNPCEpiC	eye:	n/a
28	chr3:140578726-140578776	PANC-1	pancreas:	n/a
29	chr3:140587268-140587318	K562	blood:	n/a
30	chr3:140578726-140578776	ECC-1	luminal epithelium:	n/a
31	chr3:140587268-140587318	RPTEC	kidney:	n/a
32	chr3:140587268-140587318	HRE	kidney:	n/a
33	chr3:140587268-140587318	PrEC	prostate:	n/a
34	chr3:140578726-140578776	NHBE	bronchial:	n/a
35	chr3:140578726-140578776	HRE	kidney:	n/a
36	chr3:140578726-140578776	GM12892	blood:	n/a
37	chr3:140587268-140587318	ProgFib	skin:	n/a
38	chr3:140587268-140587318	HCF	heart:	n/a
39	chr3:140587268-140587318	GM06990	blood:	n/a
40	chr3:140578726-140578776	K562	blood:	n/a
41	chr3:140587268-140587318	NH-A	brain:	n/a
42	chr3:140587268-140587318	ovcar-3	ovarian:	n/a
43	chr3:140578726-140578776	PFSK-1	brain:	n/a
44	chr3:140578726-140578776	NT2-D1	testis:	n/a
45	chr3:140587268-140587318	A549	lung:	n/a
46	chr3:140587268-140587318	HRPEpiC	eye:	n/a
47	chr3:140587268-140587318	BE2_C	brain:	n/a
48	chr3:140578726-140578776	CMK	blood:	n/a
49	chr3:140578726-140578776	HAEpiC	amniotic membrane:	n/a
50	chr3:140587268-140587318	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:140582774..140583595-chr3:140910775..140911453,2	K562	blood:
2	chr3:140567340..140568277-chrX:19340677..19341645,2	MCF-7	breast:
3	chr3:140455659..140456657-chr3:140582285..140583107,3	MCF-7	breast:
4	chr3:140271820..140272427-chr3:140582348..140582959,2	K562	blood:
5	chr3:140560323..140562507-chr3:140565228..140567400,2	MCF-7	breast:
6	chr3:140560323..140562507-chr3:140565228..140567400,2	MCF-7	breast:
7	chr3:140554185..140556969-chr3:140557455..140559405,2	MCF-7	breast:
8	chr3:140586905..140589436-chr3:140659176..140661455,2	K562	blood:
9	chr3:140554185..140556969-chr3:140557455..140559405,2	MCF-7	breast:
10	chr3:139847498..139848064-chr3:140582279..140583196,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFDP2-4	chr3:140583917-140586625	ENSG00000261826.1

Variant related genes	Relation type
ENSG00000261826	TF binding region
ENSG00000261826	CpG island
ENSG00000114120	chromatin interactions

Extended variants
information (count: 1443 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1443 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531595422	chr3:140544615-140544616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189067217	chr3:140544689-140544690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557945300	chr3:140544691-140544692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148748575	chr3:140544718-140544719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369114972	chr3:140544774-140544775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79895879	chr3:140544797-140544798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552819084	chr3:140544863-140544864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs151255941	chr3:140544864-140544865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140438804	chr3:140544892-140544893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145319130	chr3:140545034-140545035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181018111	chr3:140545090-140545091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563984996	chr3:140545091-140545092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531438848	chr3:140545125-140545126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549655339	chr3:140545154-140545155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs13062614	chr3:140545222-140545223	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs111353633	chr3:140545320-140545321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191604969	chr3:140545355-140545356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181280463	chr3:140545364-140545365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201556398	chr3:140545366-140545367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567221924	chr3:140545397-140545398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11922809	chr3:140545413-140545414	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs76588101	chr3:140545420-140545421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185923889	chr3:140545422-140545423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575983287	chr3:140545426-140545427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537549688	chr3:140545490-140545491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555621681	chr3:140545531-140545532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7619596	chr3:140545594-140545595	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs190696477	chr3:140545611-140545612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142223448	chr3:140545723-140545724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553666643	chr3:140545727-140545728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373422961	chr3:140545828-140545829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs578252338	chr3:140545876-140545877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183282524	chr3:140545928-140545929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78698221	chr3:140546039-140546040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569164130	chr3:140546051-140546052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145973047	chr3:140546203-140546204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138567883	chr3:140546277-140546278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77418385	chr3:140546298-140546299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148855905	chr3:140546340-140546341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540390784	chr3:140546384-140546385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547007047	chr3:140546439-140546440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537013474	chr3:140546475-140546476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs77198079	chr3:140546479-140546480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551433445	chr3:140546598-140546599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368953109	chr3:140546601-140546602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569824617	chr3:140546641-140546642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536883792	chr3:140546691-140546692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149778380	chr3:140546804-140546805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200334013	chr3:140546810-140546811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs143485571	chr3:140546890-140546891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Schizophrenia	17989066	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140542000-140551400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:140542800-140546400	Weak transcription	HSMMtube	muscle
3	chr3:140544200-140547000	Weak transcription	HepG2	liver
4	chr3:140546400-140547200	Enhancers	HSMMtube	muscle
5	chr3:140547000-140548400	Enhancers	HepG2	liver
6	chr3:140547200-140547400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
7	chr3:140549000-140550000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr3:140549200-140549400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr3:140549600-140551200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr3:140550000-140550400	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr3:140550400-140554400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr3:140550600-140551600	Enhancers	Primary T cells from cord blood	blood
13	chr3:140551200-140552400	Enhancers	Primary B cells from peripheral blood	blood
14	chr3:140551200-140552400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr3:140551200-140553600	Enhancers	Fetal Thymus	thymus
16	chr3:140551400-140552200	Enhancers	GM12878-XiMat	blood
17	chr3:140551400-140552400	Enhancers	Primary B cells from cord blood	blood
18	chr3:140551400-140552400	Enhancers	Primary hematopoietic stem cells	blood
19	chr3:140551400-140552400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr3:140551600-140552000	Flanking Active TSS	Primary T cells from cord blood	blood
21	chr3:140551600-140552000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr3:140551600-140552600	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr3:140552000-140552200	Enhancers	Primary T cells from cord blood	blood
24	chr3:140552000-140552400	Enhancers	Thymus	Thymus
25	chr3:140552800-140553200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr3:140552800-140553200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr3:140552800-140553400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr3:140552800-140553600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr3:140552800-140553600	Enhancers	Muscle Satellite Cultured Cells	--
30	chr3:140553000-140553400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr3:140553000-140553400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr3:140553000-140553600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr3:140553000-140553600	Enhancers	HSMM	muscle
34	chr3:140553000-140554200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr3:140553200-140553600	Enhancers	NHDF-Ad	bronchial
36	chr3:140553200-140553800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr3:140554400-140561000	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr3:140560000-140560200	Enhancers	Ovary	ovary
39	chr3:140560000-140560600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:140560200-140561200	Weak transcription	Ovary	ovary
41	chr3:140560600-140569200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:140561000-140565600	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr3:140561200-140564200	Enhancers	Ovary	ovary
44	chr3:140561400-140561800	Enhancers	GM12878-XiMat	blood
45	chr3:140561400-140565600	Enhancers	Primary B cells from peripheral blood	blood
46	chr3:140561800-140562000	Enhancers	Primary B cells from cord blood	blood
47	chr3:140561800-140562800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr3:140561800-140562800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr3:140561800-140562800	Enhancers	Right Atrium	heart
50	chr3:140561800-140563200	Flanking Active TSS	GM12878-XiMat	blood

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