Variant report

Variant	nsv879548
Chromosome Location	chr4:91558486-91661217
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	ATF2	chr4:91649067-91649556	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:91649065-91649497	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr4:91636383-91636714	GM12878	blood:	n/a	n/a
4	BCL11A	chr4:91649157-91649369	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr4:91649074-91649386	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr4:91615407-91615496	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:91628872-91628976	GM12878	blood:	n/a	n/a
8	BRCA1	chr4:91649157-91649618	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr4:91653392-91653445	GM12878	blood:	n/a	n/a
10	CEBPB	chr4:91649102-91649462	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr4:91581817-91582162	Hela-S3	cervix:	n/a	chr4:91581991-91582004 chr4:91581993-91582002 chr4:91581993-91582002 chr4:91581991-91582002 chr4:91581993-91582002
12	CEBPB	chr4:91649075-91649547	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr4:91581883-91582230	MCF-7	breast:	n/a	chr4:91581991-91582004 chr4:91581993-91582002 chr4:91581993-91582002 chr4:91581991-91582002 chr4:91581993-91582002
14	CEBPB	chr4:91572930-91573132	HepG2	liver:	n/a	chr4:91573045-91573056
15	CEBPB	chr4:91581833-91582228	A549	lung:	n/a	chr4:91581991-91582004 chr4:91581993-91582002 chr4:91581993-91582002 chr4:91581991-91582002 chr4:91581993-91582002
16	CEBPB	chr4:91649085-91649470	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr4:91581826-91582080	A549	lung:	n/a	chr4:91581991-91582004 chr4:91581993-91582002 chr4:91581993-91582002 chr4:91581991-91582002 chr4:91581993-91582002
18	CEBPB	chr4:91581812-91582169	A549	lung:	n/a	chr4:91581991-91582004 chr4:91581993-91582002 chr4:91581993-91582002 chr4:91581991-91582002 chr4:91581993-91582002
19	CEBPB	chr4:91581884-91582127	ECC-1	luminal epithelium:	n/a	chr4:91581991-91582004 chr4:91581993-91582002 chr4:91581993-91582002 chr4:91581991-91582002 chr4:91581993-91582002
20	CEBPB	chr4:91649194-91649479	MCF-7	breast:	n/a	n/a
21	CEBPB	chr4:91581839-91582171	K562	blood:	n/a	chr4:91581991-91582004 chr4:91581993-91582002 chr4:91581993-91582002 chr4:91581991-91582002 chr4:91581993-91582002
22	CEBPB	chr4:91581881-91582081	MCF-7	breast:	n/a	chr4:91581991-91582004 chr4:91581993-91582002 chr4:91581993-91582002 chr4:91581991-91582002 chr4:91581993-91582002
23	CEBPB	chr4:91581813-91582180	HepG2	liver:	n/a	chr4:91581991-91582004 chr4:91581993-91582002 chr4:91581993-91582002 chr4:91581991-91582002 chr4:91581993-91582002
24	CEBPB	chr4:91572954-91573101	A549	lung:	n/a	chr4:91573045-91573056
25	CEBPB	chr4:91581814-91582158	H1-hESC	embryonic stem cell:	n/a	chr4:91581991-91582004 chr4:91581993-91582002 chr4:91581993-91582002 chr4:91581991-91582002 chr4:91581993-91582002
26	CEBPB	chr4:91581805-91582181	IMR90	lung:	n/a	chr4:91581991-91582004 chr4:91581993-91582002 chr4:91581993-91582002 chr4:91581991-91582002 chr4:91581993-91582002
27	CHD2	chr4:91649108-91649445	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr4:91649139-91649467	Hela-S3	cervix:	n/a	n/a
29	CTBP2	chr4:91649156-91649488	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr4:91563163-91563241	HepG2	liver:	n/a	n/a
31	CTCF	chr4:91626142-91626220	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr4:91563121-91563289	Gliobla	brain:	n/a	n/a
33	CTCF	chr4:91563140-91563290	HMEC	breast:	n/a	n/a
34	CTCF	chr4:91563732-91563781	GM13977	blood:	n/a	n/a
35	CTCF	chr4:91563154-91563254	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr4:91563080-91563230	SAEC	small airway:	n/a	n/a
37	CTCF	chr4:91563100-91563250	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr4:91563160-91563310	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr4:91583327-91583418	GM13977	blood:	n/a	n/a
40	CTCF	chr4:91590640-91590790	AG10803	skin:	n/a	n/a
41	CTCF	chr4:91563100-91563250	HMEC	breast:	n/a	n/a
42	CTCF	chr4:91563140-91563290	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr4:91563140-91563290	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr4:91563040-91563190	SAEC	small airway:	n/a	n/a
45	CTCF	chr4:91563180-91563330	HAc	cerebellar:	n/a	n/a
46	E2F4	chr4:91645531-91645786	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr4:91568594-91568730	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr4:91646207-91646558	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr4:91585122-91585322	MCF10A-Er-Src	breast:	n/a	n/a
50	EBF1	chr4:91591266-91591821	GM12878	blood:	n/a	chr4:91591567-91591578

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:91570600-91570650	H1-hESC	embryonic stem cell:	embryo
2	chr4:91606776-91606826	AoSMC	blood vessel:	n/a
3	chr4:91570154-91570204	HCF	heart:	n/a
4	chr4:91606776-91606826	CMK	blood:	n/a
5	chr4:91570600-91570650	AG09319	gingival:	n/a
6	chr4:91606776-91606826	A549	lung:	n/a
7	chr4:91570154-91570204	AG04450	lung:	fetal
8	chr4:91606776-91606826	AG09309	skin:	n/a
9	chr4:91606776-91606826	HAEpiC	amniotic membrane:	n/a
10	chr4:91606776-91606826	H1-hESC	embryonic stem cell:	embryo
11	chr4:91606776-91606826	HIPEpiC	eye:	n/a
12	chr4:91606776-91606826	NT2-D1	testis:	n/a
13	chr4:91570154-91570204	HUVEC	blood vessel:	n/a
14	chr4:91570600-91570650	AG10803	skin:	n/a
15	chr4:91606776-91606826	NHBE	bronchial:	n/a
16	chr4:91570600-91570650	SK-N-SH	brain:	n/a
17	chr4:91570154-91570204	NH-A	brain:	n/a
18	chr4:91570154-91570204	NHDF-neo	bronchial:	n/a
19	chr4:91570600-91570650	SK-N-SH_RA	brain:	n/a
20	chr4:91606776-91606826	SK-N-SH_RA	brain:	n/a
21	chr4:91606776-91606826	SKMC	muscle:	n/a
22	chr4:91570600-91570650	Jurkat	blood:	n/a
23	chr4:91570600-91570650	HUVEC	blood vessel:	n/a
24	chr4:91606776-91606826	HRPEpiC	eye:	n/a
25	chr4:91570154-91570204	PFSK-1	brain:	n/a
26	chr4:91570600-91570650	HCF	heart:	n/a
27	chr4:91570600-91570650	AG09309	skin:	n/a
28	chr4:91570600-91570650	HNPCEpiC	eye:	n/a
29	chr4:91570154-91570204	HL-60	blood:	n/a
30	chr4:91570154-91570204	K562	blood:	n/a
31	chr4:91570154-91570204	PrEC	prostate:	n/a
32	chr4:91606776-91606826	RPTEC	kidney:	n/a
33	chr4:91570600-91570650	ProgFib	skin:	n/a
34	chr4:91606776-91606826	MCF10A-Er-Src	breast:	n/a
35	chr4:91570154-91570204	AoSMC	blood vessel:	n/a
36	chr4:91570600-91570650	IMR90	lung:	fetal
37	chr4:91570600-91570650	HCT-116	colon:	n/a
38	chr4:91570600-91570650	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:91570600-91570650	CMK	blood:	n/a
40	chr4:91570154-91570204	GM19239	blood:	n/a
41	chr4:91570600-91570650	MCF-7	breast:	n/a
42	chr4:91606776-91606826	PFSK-1	brain:	n/a
43	chr4:91570600-91570650	HepG2	liver:	n/a
44	chr4:91570154-91570204	HRPEpiC	eye:	n/a
45	chr4:91606776-91606826	BJ	skin:	n/a
46	chr4:91606776-91606826	Hela-S3	cervix:	n/a
47	chr4:91570154-91570204	HAEpiC	amniotic membrane:	n/a
48	chr4:91570600-91570650	SK-N-MC	brain:	n/a
49	chr4:91570154-91570204	SK-N-SH	brain:	n/a
50	chr4:91570600-91570650	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:91545051..91546944-chr4:91557103..91559359,2	MCF-7	breast:
2	chr4:91643291..91645856-chr4:91647962..91650916,2	MCF-7	breast:
3	chr4:91581426..91583883-chr4:91587486..91589501,2	MCF-7	breast:
4	chr4:91581426..91583883-chr4:91587486..91589501,2	MCF-7	breast:
5	chr4:91643291..91645856-chr4:91647962..91650916,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MMRN1-6	chr4:91645065-91645142	NONHSAT097411
2	lnc-MMRN1-6	chr4:91570659-91570775	NONHSAT097411
3	lnc-MMRN1-6	chr4:91648355-91648448	NONHSAT097411

Variant related genes	Relation type
ENSG00000251401	TF binding region
CCSER1	TF binding region
ENSG00000251401	CpG island
CCSER1	CpG island

Extended variants
information (count: 1663 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1663 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1709572	chr4:91558486-91558487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs183981857	chr4:91558501-91558502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538813040	chr4:91558511-91558512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542707965	chr4:91558523-91558524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556725836	chr4:91558541-91558542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576549547	chr4:91558574-91558575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115155952	chr4:91558597-91558598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565217445	chr4:91558607-91558608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532800159	chr4:91558625-91558626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539858158	chr4:91558667-91558668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144860547	chr4:91558778-91558779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs72871997	chr4:91558793-91558794	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs78135418	chr4:91558794-91558795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147501357	chr4:91558842-91558843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531533913	chr4:91558919-91558920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551732673	chr4:91558925-91558926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78337884	chr4:91558946-91558947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531643688	chr4:91558982-91558983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201705496	chr4:91559036-91559037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35020447	chr4:91559038-91559039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147307589	chr4:91559039-91559040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200210251	chr4:91559040-91559041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188953625	chr4:91559074-91559075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547770834	chr4:91559082-91559083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567511480	chr4:91559096-91559097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536793707	chr4:91559097-91559098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs60410989	chr4:91559100-91559101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576603705	chr4:91559121-91559122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554946045	chr4:91559140-91559141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77470501	chr4:91559166-91559167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558693358	chr4:91559205-91559206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139093271	chr4:91559217-91559218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570316372	chr4:91559224-91559225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573549716	chr4:91559257-91559258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550093634	chr4:91559281-91559282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576501033	chr4:91559323-91559324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149893619	chr4:91559328-91559329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185768459	chr4:91559335-91559336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543883312	chr4:91559395-91559396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565365815	chr4:91559424-91559425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565022971	chr4:91559427-91559428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556015122	chr4:91559495-91559496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577044113	chr4:91559590-91559591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144941129	chr4:91559594-91559595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567698231	chr4:91559637-91559638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370745324	chr4:91559684-91559685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536229498	chr4:91559753-91559754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190496488	chr4:91559770-91559771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550283328	chr4:91559848-91559849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569832342	chr4:91559856-91559857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Obesity	20622171	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91550800-91564400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:91550800-91566800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr4:91566800-91567400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:91567000-91567600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr4:91596600-91596800	Active TSS	K562	blood
6	chr4:91596600-91597000	Enhancers	Primary T cells from cord blood	blood
7	chr4:91596600-91597000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
8	chr4:91596800-91597000	Flanking Active TSS	K562	blood
9	chr4:91607000-91607600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:91607000-91608200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:91607600-91610800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:91607800-91608000	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr4:91608000-91610400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr4:91608200-91610800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:91608800-91609000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:91610200-91612000	Enhancers	HMEC	breast
17	chr4:91610400-91612200	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr4:91610600-91610800	Enhancers	NHEK	skin
19	chr4:91610600-91612000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:91610600-91612200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:91610800-91611200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:91610800-91611200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:91610800-91611200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr4:91610800-91611400	Flanking Active TSS	NHEK	skin
25	chr4:91610800-91612000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr4:91611000-91611400	Enhancers	H9 Cell Line	embryonic stem cell
27	chr4:91611400-91612200	Enhancers	NHEK	skin
28	chr4:91612200-91615600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr4:91615600-91616000	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr4:91618000-91618400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr4:91618000-91619800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:91618400-91619600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr4:91619600-91620200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr4:91628800-91629200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr4:91630600-91630800	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr4:91635400-91637000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:91640200-91640400	Enhancers	Pancreas	Pancrea
38	chr4:91643800-91644200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr4:91643800-91646200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr4:91644000-91644400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr4:91644000-91644600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr4:91644200-91644600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr4:91644200-91649200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr4:91644400-91645600	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr4:91644600-91644800	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr4:91644600-91648600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr4:91644800-91648600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr4:91645600-91645800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr4:91645800-91646200	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr4:91646200-91646400	Enhancers	HUES48 Cell Line	embryonic stem cell

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