Variant report

Variant	esv1842222
Chromosome Location	chr3:78744206-78778901
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	chr3:78771574-78771592	HepG2	liver:	n/a	n/a
2	BACH1	chr3:78775741-78775770	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:78753110-78753152	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr3:78750710-78750950	GM12878	blood:	n/a	chr3:78750822-78750831
5	BATF	chr3:78773111-78773295	GM12878	blood:	n/a	n/a
6	CEBPB	chr3:78771379-78772079	Hela-S3	cervix:	n/a	chr3:78771661-78771672
7	CEBPB	chr3:78767227-78767447	HepG2	liver:	n/a	chr3:78767291-78767302
8	CEBPB	chr3:78757805-78758086	HepG2	liver:	n/a	n/a
9	CEBPB	chr3:78750798-78750998	Hela-S3	cervix:	n/a	chr3:78750893-78750904 chr3:78750894-78750905 chr3:78750828-78750841 chr3:78750895-78750904 chr3:78750893-78750906
10	CEBPB	chr3:78771548-78772128	HepG2	liver:	n/a	chr3:78771661-78771672
11	CEBPB	chr3:78757859-78758075	A549	lung:	n/a	n/a
12	CEBPB	chr3:78750753-78751031	IMR90	lung:	n/a	chr3:78750893-78750904 chr3:78750894-78750905 chr3:78750828-78750841 chr3:78750895-78750904 chr3:78750893-78750906
13	CEBPB	chr3:78750758-78751026	HepG2	liver:	n/a	chr3:78750893-78750904 chr3:78750894-78750905 chr3:78750828-78750841 chr3:78750895-78750904 chr3:78750893-78750906
14	CTCF	chr3:78764560-78764710	GM12865	blood:	n/a	n/a
15	CTCF	chr3:78772355-78772405	GM13976	blood:	n/a	n/a
16	EBF1	chr3:78778033-78778323	GM12878	blood:	n/a	n/a
17	EBF1	chr3:78753132-78753461	GM12878	blood:	n/a	n/a
18	EBF1	chr3:78773169-78773374	GM12878	blood:	n/a	n/a
19	EBF1	chr3:78752380-78752682	GM12878	blood:	n/a	n/a
20	EP300	chr3:78774819-78775352	SK-N-SH_RA	brain:	n/a	chr3:78775186-78775200 chr3:78775318-78775332 chr3:78774899-78774913 chr3:78774996-78775010
21	EP300	chr3:78774937-78775255	SK-N-SH_RA	brain:	n/a	chr3:78775186-78775200 chr3:78774996-78775010
22	EP300	chr3:78775066-78775249	GM12878	blood:	n/a	chr3:78775186-78775200
23	EP300	chr3:78778545-78778831	SK-N-SH_RA	brain:	n/a	chr3:78778754-78778768
24	EP300	chr3:78777985-78778385	SK-N-SH_RA	brain:	n/a	chr3:78778290-78778304
25	EP300	chr3:78771655-78771797	Hela-S3	cervix:	n/a	n/a
26	FOS	chr3:78771530-78771910	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr3:78771436-78771904	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr3:78771530-78771934	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr3:78771530-78771878	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr3:78777676-78777740	MCF10A-Er-Src	breast:	n/a	n/a
31	FOXA1	chr3:78771361-78771615	T-47D	breast:	n/a	chr3:78771465-78771477
32	FOXA1	chr3:78771233-78771710	HepG2	liver:	n/a	chr3:78771465-78771477
33	FOXA1	chr3:78771250-78771575	HepG2	liver:	n/a	chr3:78771465-78771477
34	FOXA2	chr3:78771200-78771802	HepG2	liver:	n/a	chr3:78771465-78771477
35	FOXA2	chr3:78771215-78771753	A549	lung:	n/a	chr3:78771465-78771477
36	FOXA2	chr3:78771369-78771514	HepG2	liver:	n/a	chr3:78771465-78771477
37	GATA3	chr3:78774695-78775265	SK-N-SH	brain:	n/a	n/a
38	IRF1	chr3:78759909-78759911	K562	blood:	n/a	n/a
39	MAFF	chr3:78766213-78766573	K562	blood:	n/a	chr3:78766377-78766395
40	MAFF	chr3:78753102-78753411	HepG2	liver:	n/a	chr3:78753253-78753271 chr3:78753252-78753266
41	MAFF	chr3:78766163-78766585	HepG2	liver:	n/a	chr3:78766377-78766395
42	MAFK	chr3:78753212-78753305	Hela-S3	cervix:	n/a	chr3:78753252-78753266 chr3:78753251-78753267 chr3:78753249-78753269 chr3:78753255-78753265
43	MAFK	chr3:78751998-78752114	HepG2	liver:	n/a	n/a
44	MAFK	chr3:78766206-78766588	H1-hESC	embryonic stem cell:	n/a	chr3:78766379-78766394 chr3:78766379-78766390 chr3:78766379-78766390 chr3:78766378-78766392 chr3:78766380-78766391
45	MAFK	chr3:78766204-78766581	HepG2	liver:	n/a	chr3:78766379-78766394 chr3:78766379-78766390 chr3:78766379-78766390 chr3:78766378-78766392 chr3:78766380-78766391
46	MAFK	chr3:78766208-78766551	Hela-S3	cervix:	n/a	chr3:78766379-78766394 chr3:78766379-78766390 chr3:78766379-78766390 chr3:78766378-78766392 chr3:78766380-78766391
47	MAFK	chr3:78753131-78753357	IMR90	lung:	n/a	chr3:78753252-78753266 chr3:78753251-78753267 chr3:78753249-78753269 chr3:78753255-78753265
48	MAFK	chr3:78766020-78766754	GM12878	blood:	n/a	chr3:78766379-78766394 chr3:78766379-78766390 chr3:78766379-78766390 chr3:78766378-78766392 chr3:78766380-78766391
49	MAFK	chr3:78755032-78755232	HepG2	liver:	n/a	chr3:78755177-78755193 chr3:78755180-78755195 chr3:78755180-78755196
50	MAFK	chr3:78750949-78751119	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:78764742-78764792	AG09309	skin:	n/a
2	chr3:78764742-78764792	AG09309	skin:	n/a
3	chr3:78764742-78764792	HPAEpiC	pulmonary alveolar:	n/a
4	chr3:78765904-78765954	HRCEpiC	kidney:	n/a
5	chr3:78756422-78756472	U87	brain:	n/a
6	chr3:78764742-78764792	K562	blood:	n/a
7	chr3:78765904-78765954	PrEC	prostate:	n/a
8	chr3:78764742-78764792	SK-N-SH	brain:	n/a
9	chr3:78756422-78756472	PrEC	prostate:	n/a
10	chr3:78764742-78764792	AG10803	skin:	n/a
11	chr3:78764742-78764792	GM12891	blood:	n/a
12	chr3:78764742-78764792	ECC-1	luminal epithelium:	n/a
13	chr3:78756422-78756472	NB4	blood:	n/a
14	chr3:78765904-78765954	U87	brain:	n/a
15	chr3:78764742-78764792	Hela-S3	cervix:	n/a
16	chr3:78764742-78764792	ProgFib	skin:	n/a
17	chr3:78764742-78764792	HUVEC	blood vessel:	n/a
18	chr3:78765904-78765954	SK-N-SH_RA	brain:	n/a
19	chr3:78764742-78764792	HCM	heart:	n/a
20	chr3:78756422-78756472	GM12892	blood:	n/a
21	chr3:78756422-78756472	SKMC	muscle:	n/a
22	chr3:78756422-78756472	GM12891	blood:	n/a
23	chr3:78765904-78765954	T-47D	breast:	n/a
24	chr3:78764742-78764792	A549	lung:	n/a
25	chr3:78765904-78765954	MCF-7	breast:	n/a
26	chr3:78765904-78765954	HAEpiC	amniotic membrane:	n/a
27	chr3:78765904-78765954	AG04450	lung:	fetal
28	chr3:78756422-78756472	H1-hESC	embryonic stem cell:	embryo
29	chr3:78756422-78756472	AG10803	skin:	n/a
30	chr3:78764742-78764792	CMK	blood:	n/a
31	chr3:78764742-78764792	GM19239	blood:	n/a
32	chr3:78756422-78756472	Caco-2	colon:	n/a
33	chr3:78764742-78764792	BJ	skin:	n/a
34	chr3:78764742-78764792	BE2_C	brain:	n/a
35	chr3:78756422-78756472	AG04449	skin:	fetal
36	chr3:78765904-78765954	SK-N-SH	brain:	n/a
37	chr3:78765904-78765954	AG09319	gingival:	n/a
38	chr3:78765904-78765954	GM12892	blood:	n/a
39	chr3:78764742-78764792	NT2-D1	testis:	n/a
40	chr3:78756422-78756472	AG09309	skin:	n/a
41	chr3:78764742-78764792	GM06990	blood:	n/a
42	chr3:78756422-78756472	LNCaP	prostate:	n/a
43	chr3:78764742-78764792	SK-N-MC	brain:	n/a
44	chr3:78764742-78764792	Jurkat	blood:	n/a
45	chr3:78765904-78765954	AG04449	skin:	fetal
46	chr3:78765904-78765954	K562	blood:	n/a
47	chr3:78756422-78756472	T-47D	breast:	n/a
48	chr3:78765904-78765954	HCT-116	colon:	n/a
49	chr3:78764742-78764792	AG09319	gingival:	n/a
50	chr3:78764742-78764792	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:78766178..78768497-chr3:78778226..78779744,2	MCF-7	breast:
2	chr3:78741637..78744045-chr3:78754969..78756508,2	MCF-7	breast:
3	chr3:78772880..78774546-chr3:78776083..78778103,2	MCF-7	breast:
4	chr3:78766178..78768497-chr3:78778226..78779744,2	MCF-7	breast:
5	chr3:78745666..78746331-chr9:110465725..110466235,2	MCF-7	breast:
6	chr3:78753197..78755809-chr3:78927184..78929667,2	MCF-7	breast:
7	chr3:78772880..78774546-chr3:78776083..78778103,2	MCF-7	breast:

Variant related genes	Relation type
ROBO1	TF binding region
ROBO1	CpG island

Extended variants
information (count: 1406 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1406 , 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	rs9856624	chr3:78744206-78744207	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544234283	chr3:78744217-78744218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527855777	chr3:78744229-78744230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147224771	chr3:78744248-78744249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs34956966	chr3:78744266-78744267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185873870	chr3:78744299-78744300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530430043	chr3:78744325-78744326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529845183	chr3:78744326-78744327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570029611	chr3:78744345-78744346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2684377	chr3:78744383-78744384	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs552688626	chr3:78744384-78744385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140644325	chr3:78744467-78744468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533942681	chr3:78744500-78744501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529472562	chr3:78744504-78744505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189897423	chr3:78744513-78744514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573807470	chr3:78744568-78744569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536547008	chr3:78744607-78744608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10428105	chr3:78744620-78744621	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs532203928	chr3:78744623-78744624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575619302	chr3:78744624-78744625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552303445	chr3:78744638-78744639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564057235	chr3:78744645-78744646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564608407	chr3:78744683-78744684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571821461	chr3:78744707-78744708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541183813	chr3:78744772-78744773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs55684929	chr3:78744793-78744794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs67801124	chr3:78744794-78744795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145344886	chr3:78744881-78744882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs61321264	chr3:78744887-78744888	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs147679281	chr3:78744913-78744914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112326695	chr3:78744935-78744936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532526569	chr3:78744942-78744943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368786796	chr3:78744979-78744980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182117763	chr3:78744981-78744982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149800432	chr3:78745033-78745034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535127174	chr3:78745046-78745047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550581616	chr3:78745053-78745054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548443884	chr3:78745107-78745108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567448496	chr3:78745112-78745113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576754712	chr3:78745123-78745124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567299816	chr3:78745169-78745170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs59298466	chr3:78745276-78745277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34340807	chr3:78745294-78745295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs371841162	chr3:78745313-78745314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556402971	chr3:78745338-78745339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372663320	chr3:78745339-78745340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116119306	chr3:78745374-78745375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538211984	chr3:78745381-78745382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116628676	chr3:78745488-78745489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536381757	chr3:78745577-78745578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	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
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Colorectal cancer	16912164	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:78654200-78746600	Weak transcription	NHDF-Ad	bronchial
2	chr3:78667200-78751200	Weak transcription	Esophagus	oesophagus
3	chr3:78717800-78745200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr3:78717800-78748400	Weak transcription	Ovary	ovary
5	chr3:78719600-78753000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr3:78720000-78753200	Weak transcription	Brain Hippocampus Middle	brain
7	chr3:78730400-78752600	Weak transcription	Fetal Stomach	stomach
8	chr3:78733800-78744600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr3:78733800-78746600	Weak transcription	Fetal Lung	lung
10	chr3:78733800-78752400	Weak transcription	Fetal Kidney	kidney
11	chr3:78733800-78778000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:78735200-78765600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr3:78740400-78773800	Weak transcription	Brain Germinal Matrix	brain
14	chr3:78740600-78756200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr3:78742600-78756400	Weak transcription	HepG2	liver
16	chr3:78745200-78746800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr3:78746200-78746800	Enhancers	HUVEC	blood vessel
18	chr3:78746600-78747000	Enhancers	NHDF-Ad	bronchial
19	chr3:78746600-78747200	Enhancers	Fetal Lung	lung
20	chr3:78746800-78747000	Enhancers	Fetal Heart	heart
21	chr3:78746800-78749200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr3:78747000-78777400	Weak transcription	Fetal Heart	heart
23	chr3:78747200-78747800	Weak transcription	Fetal Lung	lung
24	chr3:78747800-78748000	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr3:78747800-78748000	Enhancers	Fetal Lung	lung
26	chr3:78747800-78748200	Enhancers	Brain Anterior Caudate	brain
27	chr3:78748000-78752000	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr3:78748000-78755800	Weak transcription	Fetal Lung	lung
29	chr3:78748200-78753400	Weak transcription	Brain Anterior Caudate	brain
30	chr3:78748400-78749000	Enhancers	Ovary	ovary
31	chr3:78749000-78765800	Weak transcription	Ovary	ovary
32	chr3:78749200-78749600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr3:78749600-78765600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr3:78751800-78752600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:78751800-78753400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr3:78751800-78753600	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr3:78752000-78752200	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr3:78752200-78752400	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr3:78752200-78753000	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr3:78752200-78753000	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr3:78752200-78753200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr3:78752200-78773600	Weak transcription	Stomach Smooth Muscle	stomach
43	chr3:78752400-78752600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr3:78752400-78752600	Enhancers	Fetal Kidney	kidney
45	chr3:78752400-78754000	Enhancers	Brain Substantia Nigra	brain
46	chr3:78752600-78753000	Weak transcription	Fetal Kidney	kidney
47	chr3:78752600-78755200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:78752600-78757200	Enhancers	Fetal Stomach	stomach
49	chr3:78752600-78771000	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr3:78753000-78753400	Enhancers	Brain Inferior Temporal Lobe	brain

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