Variant report

Variant	esv3415700
Chromosome Location	chr3:34806371-34914306
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	CCNT2	chr3:34854312-34854476	K562	blood:	n/a	n/a
2	CEBPB	chr3:34889620-34889898	HepG2	liver:	n/a	chr3:34889738-34889749
3	CEBPB	chr3:34889583-34889862	H1-hESC	embryonic stem cell:	n/a	chr3:34889598-34889611 chr3:34889738-34889749
4	CEBPB	chr3:34884785-34885079	HepG2	liver:	n/a	n/a
5	CEBPB	chr3:34822869-34823204	H1-hESC	embryonic stem cell:	n/a	chr3:34823023-34823034
6	CEBPB	chr3:34875174-34875446	IMR90	lung:	n/a	chr3:34875315-34875326
7	CEBPB	chr3:34851979-34852228	HepG2	liver:	n/a	chr3:34852086-34852097
8	CEBPB	chr3:34822866-34823181	IMR90	lung:	n/a	chr3:34823023-34823034
9	CEBPB	chr3:34822862-34823208	HepG2	liver:	n/a	chr3:34823023-34823034
10	CEBPB	chr3:34821753-34822045	HepG2	liver:	n/a	chr3:34821902-34821913
11	CEBPB	chr3:34875228-34875428	HepG2	liver:	n/a	chr3:34875315-34875326
12	CEBPB	chr3:34875183-34875403	A549	lung:	n/a	chr3:34875315-34875326
13	CEBPB	chr3:34822856-34823200	A549	lung:	n/a	chr3:34823023-34823034
14	CEBPB	chr3:34821777-34822055	H1-hESC	embryonic stem cell:	n/a	chr3:34821902-34821913
15	CEBPB	chr3:34889590-34889845	A549	lung:	n/a	chr3:34889598-34889611 chr3:34889738-34889749
16	CEBPB	chr3:34884755-34885113	IMR90	lung:	n/a	n/a
17	CEBPB	chr3:34875238-34875343	K562	blood:	n/a	chr3:34875315-34875326
18	CEBPB	chr3:34884810-34885083	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr3:34906980-34907102	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr3:34906725-34906775	K562	blood:	n/a	n/a
21	CTCF	chr3:34811099-34811168	GM13976	blood:	n/a	n/a
22	CTCF	chr3:34905637-34905678	LNCaP	prostate:	n/a	n/a
23	CTCF	chr3:34896960-34897110	GM12869	blood:	n/a	n/a
24	CTCF	chr3:34853378-34853456	GM10266	blood:	n/a	n/a
25	CTCF	chr3:34847939-34848010	GM13976	blood:	n/a	n/a
26	E2F4	chr3:34851079-34851260	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr3:34825317-34825719	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr3:34826207-34826403	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr3:34858112-34858312	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr3:34897540-34897740	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr3:34906950-34907126	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr3:34905506-34905766	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr3:34879652-34879805	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F6	chr3:34824359-34824764	H1-hESC	embryonic stem cell:	n/a	n/a
35	EBF1	chr3:34853376-34853479	GM12878	blood:	n/a	chr3:34853441-34853450 chr3:34853439-34853450 chr3:34853440-34853450 chr3:34853439-34853452 chr3:34853441-34853450
36	EP300	chr3:34904985-34905384	SK-N-SH_RA	brain:	n/a	chr3:34905139-34905153
37	EP300	chr3:34905030-34905329	SK-N-SH_RA	brain:	n/a	chr3:34905139-34905153
38	EP300	chr3:34892716-34893013	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr3:34904834-34905628	SK-N-SH	brain:	n/a	chr3:34905139-34905153 chr3:34904849-34904863
40	FOS	chr3:34825413-34825713	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr3:34889604-34889909	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr3:34905527-34905885	MCF10A-Er-Src	breast:	n/a	chr3:34905711-34905720 chr3:34905713-34905720 chr3:34905711-34905721 chr3:34905711-34905721 chr3:34905706-34905715
43	FOS	chr3:34905543-34905970	MCF10A-Er-Src	breast:	n/a	chr3:34905711-34905720 chr3:34905713-34905720 chr3:34905711-34905721 chr3:34905711-34905721 chr3:34905706-34905715
44	FOS	chr3:34825395-34825768	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr3:34885052-34885379	MCF10A-Er-Src	breast:	n/a	chr3:34885209-34885216 chr3:34885208-34885218 chr3:34885207-34885219 chr3:34885208-34885218 chr3:34885208-34885217 chr3:34885209-34885218
46	FOS	chr3:34825436-34825712	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr3:34889715-34889894	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr3:34885146-34885349	MCF10A-Er-Src	breast:	n/a	chr3:34885209-34885216 chr3:34885208-34885218 chr3:34885207-34885219 chr3:34885208-34885218 chr3:34885208-34885217 chr3:34885209-34885218
49	FOS	chr3:34825392-34825765	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr3:34889688-34889824	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:34884326-34884376	HRCEpiC	kidney:	n/a
2	chr3:34884326-34884376	HRCEpiC	kidney:	n/a
3	chr3:34905557-34905607	SK-N-SH	brain:	n/a
4	chr3:34884326-34884376	NHDF-neo	bronchial:	n/a
5	chr3:34884326-34884376	NH-A	brain:	n/a
6	chr3:34905557-34905607	A549	lung:	n/a
7	chr3:34905557-34905607	Hela-S3	cervix:	n/a
8	chr3:34850000-34850050	Caco-2	colon:	n/a
9	chr3:34850000-34850050	MCF-7	breast:	n/a
10	chr3:34884326-34884376	HCM	heart:	n/a
11	chr3:34884326-34884376	SKMC	muscle:	n/a
12	chr3:34884326-34884376	GM19239	blood:	n/a
13	chr3:34884326-34884376	ECC-1	luminal epithelium:	n/a
14	chr3:34850000-34850050	Hepatocyte	liver:	n/a
15	chr3:34850000-34850050	HUVEC	blood vessel:	n/a
16	chr3:34905557-34905607	AG04449	skin:	fetal
17	chr3:34850000-34850050	NH-A	brain:	n/a
18	chr3:34850000-34850050	HL-60	blood:	n/a
19	chr3:34884326-34884376	AoSMC	blood vessel:	n/a
20	chr3:34850000-34850050	AG09309	skin:	n/a
21	chr3:34850000-34850050	PANC-1	pancreas:	n/a
22	chr3:34884326-34884376	HAEpiC	amniotic membrane:	n/a
23	chr3:34905557-34905607	MCF-7	breast:	n/a
24	chr3:34905557-34905607	GM12891	blood:	n/a
25	chr3:34905557-34905607	Caco-2	colon:	n/a
26	chr3:34905557-34905607	HMEC	breast:	n/a
27	chr3:34850000-34850050	SK-N-SH_RA	brain:	n/a
28	chr3:34850000-34850050	U87	brain:	n/a
29	chr3:34905557-34905607	HRE	kidney:	n/a
30	chr3:34905557-34905607	AG09319	gingival:	n/a
31	chr3:34905557-34905607	HL-60	blood:	n/a
32	chr3:34884326-34884376	AG04449	skin:	fetal
33	chr3:34850000-34850050	ProgFib	skin:	n/a
34	chr3:34884326-34884376	AG04450	lung:	fetal
35	chr3:34884326-34884376	PANC-1	pancreas:	n/a
36	chr3:34850000-34850050	SK-N-MC	brain:	n/a
37	chr3:34850000-34850050	HIPEpiC	eye:	n/a
38	chr3:34850000-34850050	HEK293	kidney:	embryo
39	chr3:34850000-34850050	HRPEpiC	eye:	n/a
40	chr3:34850000-34850050	BE2_C	brain:	n/a
41	chr3:34905557-34905607	PANC-1	pancreas:	n/a
42	chr3:34884326-34884376	GM06990	blood:	n/a
43	chr3:34850000-34850050	AG10803	skin:	n/a
44	chr3:34850000-34850050	HRE	kidney:	n/a
45	chr3:34884326-34884376	Hepatocyte	liver:	n/a
46	chr3:34905557-34905607	HRPEpiC	eye:	n/a
47	chr3:34884326-34884376	PrEC	prostate:	n/a
48	chr3:34905557-34905607	Hepatocyte	liver:	n/a
49	chr3:34850000-34850050	HNPCEpiC	eye:	n/a
50	chr3:34884326-34884376	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:34819581..34822013-chr3:34831839..34833484,2	K562	blood:
2	chr3:34819581..34822013-chr3:34831839..34833484,2	K562	blood:
3	chr3:34888436..34891202-chr3:34891318..34893937,3	K562	blood:
4	chr3:34815559..34817841-chr3:34819019..34821368,2	K562	blood:
5	chr3:34800787..34803715-chr3:34816923..34819918,2	MCF-7	breast:
6	chr3:34888436..34891202-chr3:34891318..34893937,3	K562	blood:
7	chr3:34911721..34913497-chr3:34916113..34918111,2	K562	blood:
8	chr3:34815559..34817841-chr3:34819019..34821368,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARPP21-2	chr3:34914133-34915346	NONHSAT088963

Variant related genes	Relation type
FECHP1	TF binding region
FECHP1	CpG island

Extended variants
information (count: 2960 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2960 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs517756	chr3:34811052-34811053	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs2633355	chr3:34811068-34811069	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs577039960	chr3:34811082-34811083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146404946	chr3:34811092-34811093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2541217	chr3:34811119-34811120	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs574084138	chr3:34811134-34811135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533398666	chr3:34811137-34811138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188633558	chr3:34811165-34811166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181297093	chr3:34811192-34811193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184421907	chr3:34811254-34811255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572003203	chr3:34811340-34811341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534964872	chr3:34811345-34811346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541382535	chr3:34811403-34811404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564095967	chr3:34811426-34811427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139356705	chr3:34811454-34811455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543728380	chr3:34811461-34811462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150043040	chr3:34811471-34811472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530116372	chr3:34811495-34811496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548244122	chr3:34811505-34811506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189342869	chr3:34811523-34811524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527750151	chr3:34811574-34811575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554906172	chr3:34811587-34811588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574745996	chr3:34811594-34811595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537061655	chr3:34811616-34811617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145239442	chr3:34811622-34811623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182394429	chr3:34811651-34811652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538090900	chr3:34811665-34811666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187209156	chr3:34811684-34811685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556435885	chr3:34811697-34811698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372794405	chr3:34811700-34811701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35196363	chr3:34811728-34811729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556891336	chr3:34811730-34811731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114407111	chr3:34811756-34811757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149169130	chr3:34811833-34811834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553453406	chr3:34811842-34811843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572027513	chr3:34811855-34811856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576895769	chr3:34811866-34811867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11456197	chr3:34811949-34811950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115055645	chr3:34811955-34811956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377560390	chr3:34812031-34812032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557918461	chr3:34812039-34812040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62249354	chr3:34812066-34812067	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs543690723	chr3:34812117-34812118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4678482	chr3:34812170-34812171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs561249383	chr3:34812195-34812196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529163290	chr3:34812273-34812274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112755937	chr3:34812366-34812367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560260648	chr3:34812368-34812369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527712909	chr3:34812383-34812384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191688380	chr3:34812393-34812394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Wilms tumour	17204608	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-small cell lung cancer	21829676	CNVD
Kartagener syndrome	16639409	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34811000-34811600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:34811600-34813600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:34813600-34814000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:34814400-34815000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr3:34814600-34814800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr3:34814800-34821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr3:34817200-34817400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr3:34818000-34824200	Weak transcription	Aorta	Aorta
9	chr3:34821400-34822000	Enhancers	Fetal Heart	heart
10	chr3:34821800-34822600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr3:34821800-34823200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr3:34822600-34822800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr3:34822800-34823000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr3:34822800-34823000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr3:34822800-34823200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr3:34822800-34823200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr3:34822800-34823400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr3:34822800-34823800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr3:34823000-34824200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr3:34823200-34824200	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr3:34823200-34824400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr3:34823400-34824000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr3:34823800-34824600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:34823800-34826200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr3:34823800-34826800	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr3:34824000-34824200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr3:34824000-34824600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:34824200-34824400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr3:34824200-34824400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr3:34824200-34826200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr3:34824400-34824600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr3:34824400-34824600	Enhancers	Aorta	Aorta
33	chr3:34824400-34824800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr3:34824400-34826000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:34824400-34826200	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr3:34824400-34826600	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr3:34824600-34825200	Enhancers	Dnd41	blood
38	chr3:34824600-34826200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr3:34824800-34825200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr3:34826200-34835200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr3:34832600-34832800	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr3:34832600-34833000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:34832800-34834000	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr3:34833000-34834200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr3:34834000-34834800	Enhancers	Fetal Brain Male	brain
46	chr3:34834000-34835200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr3:34834000-34836400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr3:34834200-34836400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr3:34835200-34835400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr3:34835400-34841800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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