Variant report

Variant	nsv879559
Chromosome Location	chr4:91918870-92152678
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	chr4:92034335-92034619	HepG2	liver:	n/a	n/a
2	BACH1	chr4:92007259-92007496	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:91983060-91983121	K562	blood:	n/a	n/a
4	BCL11A	chr4:92010328-92010676	GM12878	blood:	n/a	n/a
5	BCL11A	chr4:92010407-92010604	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:92128792-92128991	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:91985692-91985806	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr4:91925193-91925259	GM12878	blood:	n/a	n/a
9	CBX3	chr4:92024996-92025295	K562	blood:	n/a	n/a
10	CEBPB	chr4:92148597-92148798	A549	lung:	n/a	chr4:92148629-92148642
11	CEBPB	chr4:92063745-92063988	A549	lung:	n/a	chr4:92063859-92063870
12	CEBPB	chr4:92148719-92148746	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr4:91986328-91986660	HepG2	liver:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
14	CEBPB	chr4:91986304-91986629	H1-hESC	embryonic stem cell:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
15	CEBPB	chr4:92061857-92062184	IMR90	lung:	n/a	chr4:92062016-92062027
16	CEBPB	chr4:91985688-91986668	Hela-S3	cervix:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
17	CEBPB	chr4:92148030-92148354	H1-hESC	embryonic stem cell:	n/a	chr4:92148264-92148277
18	CEBPB	chr4:92148015-92148366	HepG2	liver:	n/a	chr4:92148264-92148277
19	CEBPB	chr4:92148031-92148396	K562	blood:	n/a	chr4:92148264-92148277
20	CEBPB	chr4:92063721-92064028	IMR90	lung:	n/a	chr4:92063859-92063870
21	CEBPB	chr4:92063703-92064031	HepG2	liver:	n/a	chr4:92063859-92063870
22	CEBPB	chr4:92061834-92062206	HepG2	liver:	n/a	chr4:92062016-92062027
23	CEBPB	chr4:92061869-92062156	K562	blood:	n/a	chr4:92062016-92062027
24	CEBPB	chr4:91986317-91986593	A549	lung:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
25	CEBPB	chr4:91986316-91986672	K562	blood:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
26	CEBPB	chr4:92044637-92044818	H1-hESC	embryonic stem cell:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
27	CEBPB	chr4:92063832-92063977	H1-hESC	embryonic stem cell:	n/a	chr4:92063859-92063870
28	CEBPB	chr4:92061856-92062186	A549	lung:	n/a	chr4:92062016-92062027
29	CEBPB	chr4:92044617-92044895	A549	lung:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
30	CEBPB	chr4:92044571-92044854	HepG2	liver:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
31	CEBPB	chr4:92147997-92148383	A549	lung:	n/a	chr4:92148264-92148277
32	CEBPB	chr4:91986309-91986630	IMR90	lung:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
33	CEBPB	chr4:92148021-92148389	Hela-S3	cervix:	n/a	chr4:92148264-92148277
34	CEBPB	chr4:92148019-92148382	IMR90	lung:	n/a	chr4:92148264-92148277
35	CEBPB	chr4:91974973-91975287	HepG2	liver:	n/a	chr4:91975130-91975141
36	CEBPB	chr4:92007232-92007488	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:91986318-91986568	ECC-1	luminal epithelium:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
38	CEBPB	chr4:92034320-92034601	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPZ	chr4:92031768-92031775	HepG2	liver:	n/a	n/a
40	CHD1	chr4:92143874-92143897	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr4:91946453-91946857	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr4:91946512-91946765	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr4:92034383-92034669	HCT-116	colon:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
44	CTCF	chr4:92034320-92034470	HRE	kidney:	n/a	n/a
45	CTCF	chr4:92034380-92034530	GM06990	blood:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
46	CTCF	chr4:92034420-92034570	HFF	foreskin:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
47	CTCF	chr4:92037959-92038514	HCT-116	colon:	n/a	chr4:92038207-92038228
48	CTCF	chr4:91922731-91922808	GM10266	blood:	n/a	n/a
49	CTCF	chr4:92034360-92034510	AoAF	blood vessel:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
50	CTCF	chr4:92038160-92038310	HUVEC	blood vessel:	n/a	chr4:92038207-92038228

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:92089238-92089288	U87	brain:	n/a
2	chr4:92008475-92008525	HRCEpiC	kidney:	n/a
3	chr4:92008475-92008525	HCPEpiC	choroid plexus:	n/a
4	chr4:92008475-92008525	AG04450	lung:	fetal
5	chr4:92048256-92048306	PANC-1	pancreas:	n/a
6	chr4:92008475-92008525	MCF10A-Er-Src	breast:	n/a
7	chr4:92008475-92008525	AoSMC	blood vessel:	n/a
8	chr4:92089238-92089288	AG04449	skin:	fetal
9	chr4:92048256-92048306	HUVEC	blood vessel:	n/a
10	chr4:92048256-92048306	AG09319	gingival:	n/a
11	chr4:92089238-92089288	GM19239	blood:	n/a
12	chr4:92089238-92089288	HepG2	liver:	n/a
13	chr4:92008475-92008525	HEEpiC	esophagus:	n/a
14	chr4:92089238-92089288	Hepatocyte	liver:	n/a
15	chr4:92034737-92034787	GM06990	blood:	n/a
16	chr4:92048256-92048306	Hepatocyte	liver:	n/a
17	chr4:92034737-92034787	GM12878	blood:	n/a
18	chr4:92089238-92089288	GM12891	blood:	n/a
19	chr4:92034737-92034787	AG10803	skin:	n/a
20	chr4:92048256-92048306	IMR90	lung:	fetal
21	chr4:92089238-92089288	HCF	heart:	n/a
22	chr4:92048256-92048306	ECC-1	luminal epithelium:	n/a
23	chr4:92048256-92048306	SAEC	small airway:	n/a
24	chr4:92008475-92008525	AG09319	gingival:	n/a
25	chr4:92089238-92089288	IMR90	lung:	fetal
26	chr4:92034737-92034787	NH-A	brain:	n/a
27	chr4:92008475-92008525	GM06990	blood:	n/a
28	chr4:92048256-92048306	AG04449	skin:	fetal
29	chr4:92048256-92048306	BJ	skin:	n/a
30	chr4:92048256-92048306	HCPEpiC	choroid plexus:	n/a
31	chr4:92008475-92008525	ECC-1	luminal epithelium:	n/a
32	chr4:92048256-92048306	GM06990	blood:	n/a
33	chr4:92034737-92034787	MCF-7	breast:	n/a
34	chr4:92089238-92089288	HRE	kidney:	n/a
35	chr4:92089238-92089288	HL-60	blood:	n/a
36	chr4:92034737-92034787	NHBE	bronchial:	n/a
37	chr4:92034737-92034787	ovcar-3	ovarian:	n/a
38	chr4:92034737-92034787	HCF	heart:	n/a
39	chr4:92008475-92008525	K562	blood:	n/a
40	chr4:92008475-92008525	Hela-S3	cervix:	n/a
41	chr4:92048256-92048306	HL-60	blood:	n/a
42	chr4:92089238-92089288	AoSMC	blood vessel:	n/a
43	chr4:92089238-92089288	NT2-D1	testis:	n/a
44	chr4:92034737-92034787	RPTEC	kidney:	n/a
45	chr4:92034737-92034787	Caco-2	colon:	n/a
46	chr4:92089238-92089288	Jurkat	blood:	n/a
47	chr4:92034737-92034787	HPAEpiC	pulmonary alveolar:	n/a
48	chr4:92034737-92034787	BJ	skin:	n/a
49	chr4:92048256-92048306	NH-A	brain:	n/a
50	chr4:92034737-92034787	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:91903199..91905652-chr4:91956772..91959683,2	MCF-7	breast:
2	chr4:92034306..92035417-chr4:92423226..92424074,5	MCF-7	breast:
3	chr4:91971782..91973495-chr4:91983792..91985364,2	MCF-7	breast:
4	chr10:82295674..82298297-chr4:92009865..92012633,2	MCF-7	breast:
5	chr4:91871450..91872421-chr4:91953829..91954477,2	MCF-7	breast:
6	chr4:91938775..91940847-chr4:91941270..91944151,2	K562	blood:
7	chr4:91971782..91973495-chr4:91983792..91985364,2	MCF-7	breast:
8	chr4:91938775..91940847-chr4:91941270..91944151,2	K562	blood:
9	chr4:92118886..92121028-chr6:31337898..31340855,2	MCF-7	breast:
10	chr4:91982821..91984547-chr4:91990420..91991992,2	MCF-7	breast:
11	chr4:91982821..91984547-chr4:91990420..91991992,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-763F8.1.1-1	chr4:92029174-92029251	ENSG00000248984.1
2	lnc-RP11-763F8.1.1-1	chr4:92033750-92033941	ENSG00000248984.1

Variant related genes	Relation type
ENSG00000248984	TF binding region
ENSG00000248984	CpG island
ENSG00000226659	chromatin interactions
ENSG00000178217	chromatin interactions
ENSG00000201658	chromatin interactions

Extended variants
information (count: 4798 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4798 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189343785	chr4:91924438-91924439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs146236836	chr4:91924448-91924449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181330835	chr4:91924480-91924481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116032473	chr4:91924545-91924546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560332210	chr4:91924548-91924549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545336160	chr4:91924568-91924569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528126569	chr4:91924569-91924570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548310677	chr4:91924574-91924575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs118129612	chr4:91924614-91924615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561514915	chr4:91924622-91924623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564111703	chr4:91924624-91924625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550578153	chr4:91924633-91924634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572476792	chr4:91924636-91924637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140102607	chr4:91924652-91924653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs367785604	chr4:91924692-91924693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186335986	chr4:91924752-91924753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535951971	chr4:91924770-91924771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555870402	chr4:91924796-91924797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs28524051	chr4:91924812-91924813	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs76914501	chr4:91924834-91924835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75298778	chr4:91924864-91924865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111408346	chr4:91924887-91924888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540536306	chr4:91924890-91924891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111601102	chr4:91924898-91924899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373525870	chr4:91924922-91924923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573935259	chr4:91924925-91924926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143687158	chr4:91924947-91924948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146790353	chr4:91924988-91924989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376944593	chr4:91925023-91925024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529100137	chr4:91925052-91925053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139229691	chr4:91925064-91925065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369284784	chr4:91925069-91925070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564078677	chr4:91925077-91925078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114335457	chr4:91925085-91925086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10440322	chr4:91925115-91925116	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs566662926	chr4:91925117-91925118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371573234	chr4:91925136-91925137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs117416216	chr4:91925142-91925143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549188035	chr4:91925161-91925162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375775528	chr4:91925223-91925224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569308835	chr4:91925233-91925234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78856741	chr4:91925235-91925236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150068047	chr4:91925261-91925262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369498292	chr4:91925262-91925263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528581365	chr4:91925270-91925271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72884761	chr4:91925283-91925284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554077567	chr4:91925305-91925306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573871600	chr4:91925323-91925324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373996675	chr4:91925339-91925340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551359951	chr4:91925366-91925367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Esophageal adenocarcinoma	18519675	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:315 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91924400-91924800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:91924600-91924800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:91924800-91933400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:91925800-91930000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:91928400-91928800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr4:91930000-91930400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:91930400-91932600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:91932600-91933000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:91933600-91933800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr4:91939400-91941000	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:91939600-91941000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr4:91939600-91941000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr4:91940400-91941000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr4:91941800-91948000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr4:91946600-91947400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr4:91946600-91947400	Enhancers	Fetal Lung	lung
17	chr4:91947000-91947400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr4:91954000-91954600	Enhancers	Pancreas	Pancrea
19	chr4:91954600-91958400	Weak transcription	Pancreas	Pancrea
20	chr4:91956400-91957200	Enhancers	Colon Smooth Muscle	Colon
21	chr4:91957200-91958400	Weak transcription	Colon Smooth Muscle	Colon
22	chr4:91958400-91958600	Enhancers	Colon Smooth Muscle	Colon
23	chr4:91958400-91958600	Enhancers	Pancreas	Pancrea
24	chr4:91961600-91961800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr4:91961600-91962000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr4:91961600-91962000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr4:91961600-91962400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr4:91961800-91962000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr4:91972600-91985400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr4:91977800-91978000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:91978000-91978600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:91978400-91979600	Enhancers	HMEC	breast
33	chr4:91978600-91978800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:91978600-91979600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr4:91978600-91980200	Enhancers	NHEK	skin
36	chr4:91978800-91984600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:91979000-91979600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr4:91979200-91979400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:91980200-91985400	Weak transcription	NHEK	skin
40	chr4:91980800-91981200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr4:91980800-91981400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr4:91981000-91981400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:91981200-91985200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:91981400-91985400	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr4:91981400-91985400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr4:91983400-91983600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr4:91984200-91986400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr4:91984600-91985400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:91984600-91985600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:91984600-91985600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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