Variant report

Variant	nsv834654
Chromosome Location	chr3:34747802-34916657
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:272)
CpG islands
(count:244)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:34751314-34751326	K562	blood:	n/a	n/a
2	BATF	chr3:34769260-34769568	GM12878	blood:	n/a	chr3:34769375-34769386
3	BATF	chr3:34769285-34769510	GM12878	blood:	n/a	chr3:34769375-34769386
4	BCL11A	chr3:34769277-34769512	GM12878	blood:	n/a	n/a
5	CCNT2	chr3:34854312-34854476	K562	blood:	n/a	n/a
6	CEBPB	chr3:34884755-34885113	IMR90	lung:	n/a	n/a
7	CEBPB	chr3:34821777-34822055	H1-hESC	embryonic stem cell:	n/a	chr3:34821902-34821913
8	CEBPB	chr3:34851979-34852228	HepG2	liver:	n/a	chr3:34852086-34852097
9	CEBPB	chr3:34822862-34823208	HepG2	liver:	n/a	chr3:34823023-34823034
10	CEBPB	chr3:34875228-34875428	HepG2	liver:	n/a	chr3:34875315-34875326
11	CEBPB	chr3:34795469-34795717	HepG2	liver:	n/a	chr3:34795548-34795561 chr3:34795548-34795559
12	CEBPB	chr3:34822869-34823204	H1-hESC	embryonic stem cell:	n/a	chr3:34823023-34823034
13	CEBPB	chr3:34875183-34875403	A549	lung:	n/a	chr3:34875315-34875326
14	CEBPB	chr3:34875174-34875446	IMR90	lung:	n/a	chr3:34875315-34875326
15	CEBPB	chr3:34889620-34889898	HepG2	liver:	n/a	chr3:34889738-34889749
16	CEBPB	chr3:34889590-34889845	A549	lung:	n/a	chr3:34889598-34889611 chr3:34889738-34889749
17	CEBPB	chr3:34821753-34822045	HepG2	liver:	n/a	chr3:34821902-34821913
18	CEBPB	chr3:34875238-34875343	K562	blood:	n/a	chr3:34875315-34875326
19	CEBPB	chr3:34884810-34885083	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:34822866-34823181	IMR90	lung:	n/a	chr3:34823023-34823034
21	CEBPB	chr3:34889583-34889862	H1-hESC	embryonic stem cell:	n/a	chr3:34889598-34889611 chr3:34889738-34889749
22	CEBPB	chr3:34822856-34823200	A549	lung:	n/a	chr3:34823023-34823034
23	CEBPB	chr3:34884785-34885079	HepG2	liver:	n/a	n/a
24	CHD2	chr3:34906725-34906775	K562	blood:	n/a	n/a
25	CHD2	chr3:34906980-34907102	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr3:34853378-34853456	GM10266	blood:	n/a	n/a
27	CTCF	chr3:34811099-34811168	GM13976	blood:	n/a	n/a
28	CTCF	chr3:34847939-34848010	GM13976	blood:	n/a	n/a
29	CTCF	chr3:34896960-34897110	GM12869	blood:	n/a	n/a
30	CTCF	chr3:34803538-34803551	GM10248	blood:	n/a	n/a
31	CTCF	chr3:34784660-34784810	GM12869	blood:	n/a	n/a
32	CTCF	chr3:34905637-34905678	LNCaP	prostate:	n/a	n/a
33	E2F4	chr3:34858112-34858312	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr3:34905506-34905766	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr3:34879652-34879805	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr3:34825317-34825719	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr3:34851079-34851260	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr3:34897540-34897740	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr3:34906950-34907126	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr3:34826207-34826403	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr3:34747792-34747826	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F6	chr3:34824359-34824764	H1-hESC	embryonic stem cell:	n/a	n/a
43	EBF1	chr3:34853376-34853479	GM12878	blood:	n/a	chr3:34853441-34853450 chr3:34853439-34853450 chr3:34853440-34853450 chr3:34853439-34853452 chr3:34853441-34853450
44	EP300	chr3:34904985-34905384	SK-N-SH_RA	brain:	n/a	chr3:34905139-34905153
45	EP300	chr3:34892716-34893013	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr3:34905030-34905329	SK-N-SH_RA	brain:	n/a	chr3:34905139-34905153
47	EP300	chr3:34904834-34905628	SK-N-SH	brain:	n/a	chr3:34905139-34905153 chr3:34904849-34904863
48	EP300	chr3:34795811-34795835	GM12878	blood:	n/a	n/a
49	FOS	chr3:34825436-34825712	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr3:34825392-34825765	MCF10A-Er-Src	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:34767621-34767671	IMR90	lung:	fetal
2	chr3:34850000-34850050	IMR90	lung:	fetal
3	chr3:34905557-34905607	SK-N-SH	brain:	n/a
4	chr3:34884326-34884376	MCF10A-Er-Src	breast:	n/a
5	chr3:34767621-34767671	BJ	skin:	n/a
6	chr3:34905557-34905607	Jurkat	blood:	n/a
7	chr3:34884326-34884376	NT2-D1	testis:	n/a
8	chr3:34850000-34850050	HEK293	kidney:	embryo
9	chr3:34767621-34767671	SKMC	muscle:	n/a
10	chr3:34884326-34884376	AG09309	skin:	n/a
11	chr3:34884326-34884376	K562	blood:	n/a
12	chr3:34884326-34884376	HRE	kidney:	n/a
13	chr3:34884326-34884376	Hela-S3	cervix:	n/a
14	chr3:34850000-34850050	CMK	blood:	n/a
15	chr3:34905557-34905607	PrEC	prostate:	n/a
16	chr3:34884326-34884376	HEEpiC	esophagus:	n/a
17	chr3:34850000-34850050	ECC-1	luminal epithelium:	n/a
18	chr3:34884326-34884376	LNCaP	prostate:	n/a
19	chr3:34850000-34850050	ovcar-3	ovarian:	n/a
20	chr3:34905557-34905607	HPAEpiC	pulmonary alveolar:	n/a
21	chr3:34767621-34767671	AG04450	lung:	fetal
22	chr3:34850000-34850050	NHDF-neo	bronchial:	n/a
23	chr3:34905557-34905607	GM12878	blood:	n/a
24	chr3:34884326-34884376	Jurkat	blood:	n/a
25	chr3:34884326-34884376	HCF	heart:	n/a
26	chr3:34905557-34905607	K562	blood:	n/a
27	chr3:34767621-34767671	GM12892	blood:	n/a
28	chr3:34850000-34850050	T-47D	breast:	n/a
29	chr3:34850000-34850050	Hepatocyte	liver:	n/a
30	chr3:34850000-34850050	PrEC	prostate:	n/a
31	chr3:34850000-34850050	AG09309	skin:	n/a
32	chr3:34884326-34884376	HRCEpiC	kidney:	n/a
33	chr3:34905557-34905607	HEEpiC	esophagus:	n/a
34	chr3:34884326-34884376	NB4	blood:	n/a
35	chr3:34767621-34767671	NT2-D1	testis:	n/a
36	chr3:34884326-34884376	ProgFib	skin:	n/a
37	chr3:34884326-34884376	Hepatocyte	liver:	n/a
38	chr3:34850000-34850050	HPAEpiC	pulmonary alveolar:	n/a
39	chr3:34884326-34884376	Caco-2	colon:	n/a
40	chr3:34905557-34905607	U87	brain:	n/a
41	chr3:34850000-34850050	HCM	heart:	n/a
42	chr3:34905557-34905607	GM12891	blood:	n/a
43	chr3:34884326-34884376	BE2_C	brain:	n/a
44	chr3:34850000-34850050	GM12892	blood:	n/a
45	chr3:34767621-34767671	LNCaP	prostate:	n/a
46	chr3:34850000-34850050	NT2-D1	testis:	n/a
47	chr3:34905557-34905607	MCF10A-Er-Src	breast:	n/a
48	chr3:34905557-34905607	HL-60	blood:	n/a
49	chr3:34767621-34767671	H1-hESC	embryonic stem cell:	embryo
50	chr3:34884326-34884376	HCT-116	colon:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:34759474..34761500-chr3:34763311..34766197,2	K562	blood:
2	chr3:34911721..34913497-chr3:34916113..34918111,2	K562	blood:
3	chr3:34888436..34891202-chr3:34891318..34893937,3	K562	blood:
4	chr3:34815559..34817841-chr3:34819019..34821368,2	K562	blood:
5	chr3:34819581..34822013-chr3:34831839..34833484,2	K562	blood:
6	chr3:34819581..34822013-chr3:34831839..34833484,2	K562	blood:
7	chr3:34800787..34803715-chr3:34816923..34819918,2	MCF-7	breast:
8	chr3:34759474..34761500-chr3:34763311..34766197,2	K562	blood:
9	chr3:34888436..34891202-chr3:34891318..34893937,3	K562	blood:
10	chr3:34911721..34913497-chr3:34916113..34918111,2	K562	blood:
11	chr3:34815559..34817841-chr3:34819019..34821368,2	K562	blood:
12	chr3:34800787..34803715-chr3:34816923..34819918,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 3935 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3935 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187253837	chr3:34757025-34757026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561005595	chr3:34757094-34757095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192035860	chr3:34757163-34757164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534600963	chr3:34757164-34757165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371401236	chr3:34757199-34757200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528566429	chr3:34757249-34757250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546761722	chr3:34757284-34757285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138588948	chr3:34757308-34757309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532673072	chr3:34757309-34757310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184166027	chr3:34757324-34757325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs74950455	chr3:34757327-34757328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs386660094	chr3:34757366-34757367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571216738	chr3:34757375-34757376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186037025	chr3:34757385-34757386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190804360	chr3:34757393-34757394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566546816	chr3:34757400-34757401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182500191	chr3:34757407-34757408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558767396	chr3:34757415-34757416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577136517	chr3:34757424-34757425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537744592	chr3:34757458-34757459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556461994	chr3:34757459-34757460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116652191	chr3:34757478-34757479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs17032086	chr3:34757534-34757535	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs560968031	chr3:34757544-34757545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1362538	chr3:34757569-34757570	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs187201478	chr3:34757621-34757622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79561984	chr3:34757669-34757670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549767402	chr3:34757692-34757693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550905959	chr3:34757701-34757702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192586010	chr3:34757715-34757716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114096448	chr3:34757722-34757723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369210410	chr3:34757725-34757726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548175454	chr3:34757754-34757755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73824744	chr3:34757755-34757756	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs62249292	chr3:34757760-34757761	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs187967565	chr3:34757789-34757790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1420507	chr3:34757790-34757791	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs538003459	chr3:34757815-34757816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552286821	chr3:34757820-34757821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571910200	chr3:34757837-34757838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556088367	chr3:34757841-34757842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs193065852	chr3:34757853-34757854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369247787	chr3:34757867-34757868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535400554	chr3:34757903-34757904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372239984	chr3:34757932-34757933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572949236	chr3:34757958-34757959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112180125	chr3:34757960-34757961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149260252	chr3:34758162-34758163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146211019	chr3:34758220-34758221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114272714	chr3:34758223-34758224	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:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34757000-34767400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:34758000-34758200	Enhancers	Pancreas	Pancrea
3	chr3:34758200-34767800	Weak transcription	Pancreas	Pancrea
4	chr3:34765000-34765200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr3:34765600-34766000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:34765600-34767600	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr3:34766000-34766400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr3:34766000-34767200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:34766600-34767400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr3:34766600-34768000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr3:34767000-34767400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr3:34767000-34767800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr3:34767000-34768000	Enhancers	Fetal Heart	heart
14	chr3:34767200-34768000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:34767400-34768000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr3:34767400-34768000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:34767600-34767800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr3:34767800-34768000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr3:34767800-34768000	Enhancers	Pancreas	Pancrea
20	chr3:34768000-34772800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr3:34768000-34773000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr3:34772800-34773800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:34773000-34773400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr3:34773000-34773400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr3:34773000-34773800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr3:34773000-34773800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr3:34773000-34774000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr3:34773200-34773600	Enhancers	Fetal Muscle Trunk	muscle
29	chr3:34773400-34773800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr3:34773800-34774200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr3:34774200-34774400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr3:34774400-34776400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr3:34776000-34776200	Enhancers	Fetal Heart	heart
34	chr3:34776200-34777200	Weak transcription	Fetal Heart	heart
35	chr3:34777200-34777800	Enhancers	Fetal Heart	heart
36	chr3:34778200-34779200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:34779200-34779400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:34783800-34784600	Enhancers	Fetal Muscle Leg	muscle
39	chr3:34800400-34801000	Enhancers	Fetal Muscle Leg	muscle
40	chr3:34811000-34811600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr3:34811600-34813600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr3:34813600-34814000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr3:34814400-34815000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr3:34814600-34814800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr3:34814800-34821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr3:34817200-34817400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:34818000-34824200	Weak transcription	Aorta	Aorta
48	chr3:34821400-34822000	Enhancers	Fetal Heart	heart
49	chr3:34821800-34822600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr3:34821800-34823200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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