Variant report

Variant	nsv879612
Chromosome Location	chr4:93761619-93969165
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	chr4:93915938-93916211	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:93890976-93891589	HepG2	liver:	n/a	n/a
3	ATF3	chr4:93891072-93891445	A549	lung:	n/a	n/a
4	ATF3	chr4:93891228-93891471	A549	lung:	n/a	n/a
5	BACH1	chr4:93967370-93967376	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr4:93951903-93952165	GM12878	blood:	n/a	n/a
7	BATF	chr4:93951951-93952159	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:93951916-93952178	GM12878	blood:	n/a	n/a
9	BCL3	chr4:93891030-93891647	A549	lung:	n/a	n/a
10	BHLHE40	chr4:93951978-93952126	GM12878	blood:	n/a	n/a
11	BRCA1	chr4:93890921-93891508	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr4:93891028-93891487	HCT-116	colon:	n/a	n/a
13	CEBPB	chr4:93835580-93835776	HepG2	liver:	n/a	chr4:93835654-93835665
14	CEBPB	chr4:93909521-93909888	Hela-S3	cervix:	n/a	chr4:93909702-93909713 chr4:93909783-93909794
15	CEBPB	chr4:93891114-93891468	HepG2	liver:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
16	CEBPB	chr4:93847042-93847319	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:93965211-93965515	A549	lung:	n/a	chr4:93965391-93965400 chr4:93965389-93965402 chr4:93965389-93965400 chr4:93965391-93965400 chr4:93965391-93965400 chr4:93965444-93965457 chr4:93965391-93965400 chr4:93965391-93965402
18	CEBPB	chr4:93940029-93940374	IMR90	lung:	n/a	chr4:93940211-93940224 chr4:93940212-93940223 chr4:93940144-93940157
19	CEBPB	chr4:93901112-93901404	HepG2	liver:	n/a	chr4:93901280-93901291
20	CEBPB	chr4:93909565-93909866	A549	lung:	n/a	chr4:93909702-93909713 chr4:93909783-93909794
21	CEBPB	chr4:93916625-93916817	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:93952911-93953173	HepG2	liver:	n/a	chr4:93953046-93953057
23	CEBPB	chr4:93795845-93796108	HepG2	liver:	n/a	chr4:93795963-93795974
24	CEBPB	chr4:93806171-93806461	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:93965207-93965565	HepG2	liver:	n/a	chr4:93965391-93965400 chr4:93965389-93965402 chr4:93965389-93965400 chr4:93965391-93965400 chr4:93965391-93965400 chr4:93965444-93965457 chr4:93965391-93965400 chr4:93965391-93965402
26	CEBPB	chr4:93952882-93953196	IMR90	lung:	n/a	chr4:93953046-93953057
27	CEBPB	chr4:93909536-93909890	IMR90	lung:	n/a	chr4:93909702-93909713 chr4:93909783-93909794
28	CEBPB	chr4:93916641-93916775	A549	lung:	n/a	n/a
29	CEBPB	chr4:93964448-93964650	A549	lung:	n/a	chr4:93964542-93964553
30	CEBPB	chr4:93891071-93891477	A549	lung:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
31	CEBPB	chr4:93795868-93796039	IMR90	lung:	n/a	chr4:93795963-93795974
32	CEBPB	chr4:93891126-93891368	HepG2	liver:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
33	CEBPB	chr4:93933534-93933802	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:93891027-93891542	MCF-7	breast:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
35	CEBPB	chr4:93873627-93873920	HepG2	liver:	n/a	chr4:93873803-93873814 chr4:93873761-93873772 chr4:93873801-93873812
36	CEBPB	chr4:93964448-93964712	HepG2	liver:	n/a	chr4:93964542-93964553
37	CEBPB	chr4:93891205-93891410	HepG2	liver:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
38	CEBPB	chr4:93847023-93847348	A549	lung:	n/a	n/a
39	CEBPB	chr4:93890872-93891520	HepG2	liver:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
40	CEBPB	chr4:93886193-93886419	HepG2	liver:	n/a	chr4:93886329-93886340
41	CEBPB	chr4:93890804-93891725	MCF-7	breast:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
42	CEBPB	chr4:93909540-93909893	HepG2	liver:	n/a	chr4:93909702-93909713 chr4:93909783-93909794
43	CEBPB	chr4:93890906-93891682	HCT-116	colon:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
44	CEBPB	chr4:93890512-93891528	Hela-S3	cervix:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
45	CEBPB	chr4:93901011-93901535	MCF-7	breast:	n/a	chr4:93901280-93901291
46	CEBPB	chr4:93891066-93891516	IMR90	lung:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
47	CEBPB	chr4:93940036-93940289	Hela-S3	cervix:	n/a	chr4:93940211-93940224 chr4:93940212-93940223 chr4:93940144-93940157
48	CEBPB	chr4:93915947-93916152	HepG2	liver:	n/a	n/a
49	CEBPB	chr4:93909470-93909870	A549	lung:	n/a	chr4:93909702-93909713 chr4:93909783-93909794
50	CEBPB	chr4:93909571-93909844	K562	blood:	n/a	chr4:93909702-93909713 chr4:93909783-93909794

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:93930622-93930672	ProgFib	skin:	n/a
2	chr4:93930622-93930672	SK-N-SH	brain:	n/a
3	chr4:93930622-93930672	AG09319	gingival:	n/a
4	chr4:93930622-93930672	AG04450	lung:	fetal
5	chr4:93930622-93930672	AG10803	skin:	n/a
6	chr4:93930622-93930672	Caco-2	colon:	n/a
7	chr4:93930622-93930672	K562	blood:	n/a
8	chr4:93930622-93930672	HUVEC	blood vessel:	n/a
9	chr4:93930622-93930672	HIPEpiC	eye:	n/a
10	chr4:93930622-93930672	HPAEpiC	pulmonary alveolar:	n/a
11	chr4:93930622-93930672	MCF-7	breast:	n/a
12	chr4:93930622-93930672	SAEC	small airway:	n/a
13	chr4:93930622-93930672	HCPEpiC	choroid plexus:	n/a
14	chr4:93930622-93930672	HMEC	breast:	n/a
15	chr4:93930622-93930672	NH-A	brain:	n/a
16	chr4:93930622-93930672	AoSMC	blood vessel:	n/a
17	chr4:93930622-93930672	HCT-116	colon:	n/a
18	chr4:93930622-93930672	IMR90	lung:	fetal
19	chr4:93930622-93930672	HCF	heart:	n/a
20	chr4:93930622-93930672	SKMC	muscle:	n/a
21	chr4:93930622-93930672	GM19239	blood:	n/a
22	chr4:93930622-93930672	Jurkat	blood:	n/a
23	chr4:93930622-93930672	H1-hESC	embryonic stem cell:	embryo
24	chr4:93930622-93930672	HRE	kidney:	n/a
25	chr4:93930622-93930672	BJ	skin:	n/a
26	chr4:93930622-93930672	CMK	blood:	n/a
27	chr4:93930622-93930672	HRPEpiC	eye:	n/a
28	chr4:93930622-93930672	SK-N-SH_RA	brain:	n/a
29	chr4:93930622-93930672	SK-N-MC	brain:	n/a
30	chr4:93930622-93930672	ovcar-3	ovarian:	n/a
31	chr4:93930622-93930672	HCM	heart:	n/a
32	chr4:93930622-93930672	MCF10A-Er-Src	breast:	n/a
33	chr4:93930622-93930672	BE2_C	brain:	n/a
34	chr4:93930622-93930672	GM12878	blood:	n/a
35	chr4:93930622-93930672	U87	brain:	n/a
36	chr4:93930622-93930672	LNCaP	prostate:	n/a
37	chr4:93930622-93930672	HL-60	blood:	n/a
38	chr4:93930622-93930672	HNPCEpiC	eye:	n/a
39	chr4:93930622-93930672	T-47D	breast:	n/a
40	chr4:93930622-93930672	PFSK-1	brain:	n/a
41	chr4:93930622-93930672	HEK293	kidney:	embryo
42	chr4:93930622-93930672	HEEpiC	esophagus:	n/a
43	chr4:93930622-93930672	RPTEC	kidney:	n/a
44	chr4:93930622-93930672	GM12891	blood:	n/a
45	chr4:93930622-93930672	PrEC	prostate:	n/a
46	chr4:93930622-93930672	AG04449	skin:	fetal
47	chr4:93930622-93930672	Hela-S3	cervix:	n/a
48	chr4:93930622-93930672	A549	lung:	n/a
49	chr4:93930622-93930672	NT2-D1	testis:	n/a
50	chr4:93930622-93930672	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:93922270..93924469-chr4:93926058..93927823,2	MCF-7	breast:
2	chr4:93886231..93887821-chr4:93901908..93903959,2	K562	blood:
3	chr4:93827426..93829042-chr4:93829198..93830745,2	K562	blood:
4	chr4:93922270..93924469-chr4:93926058..93927823,2	MCF-7	breast:
5	chr4:93968750..93971596-chr4:93971794..93974511,2	MCF-7	breast:
6	chr4:93825096..93827296-chr4:93828128..93830318,2	K562	blood:
7	chr4:93846312..93847841-chr4:93851226..93853929,2	K562	blood:
8	chr4:93920911..93923301-chr4:93923626..93925669,2	MCF-7	breast:
9	chr4:93773449..93776266-chr4:93779103..93780772,2	MCF-7	breast:
10	chr4:93908293..93911044-chr4:93911588..93914279,2	MCF-7	breast:
11	chr4:93920911..93923301-chr4:93923626..93925669,2	MCF-7	breast:
12	chr4:93846312..93847841-chr4:93851226..93853929,2	K562	blood:
13	chr4:93827426..93829042-chr4:93829198..93830745,2	K562	blood:
14	chr4:93825096..93827296-chr4:93828128..93830318,2	K562	blood:
15	chr4:93886231..93887821-chr4:93901908..93903959,2	K562	blood:
16	chr4:93757984..93759775-chr4:93817140..93819795,2	MCF-7	breast:
17	chr4:93908293..93911044-chr4:93911588..93914279,2	MCF-7	breast:
18	chr4:93773449..93776266-chr4:93779103..93780772,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATOH1-1	chr4:93805814-93806258	NONHSAT097436

Variant related genes	Relation type
ENSG00000248750	TF binding region
ENSG00000248627	TF binding region
ENSG00000248750	CpG island
ENSG00000248627	CpG island

Extended variants
information (count: 5098 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:5098 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs892664	chr4:93761619-93761620	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115261438	chr4:93761676-93761677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188399902	chr4:93761687-93761688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569143127	chr4:93761801-93761802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116617628	chr4:93761812-93761813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558253701	chr4:93761835-93761836	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs114085977	chr4:93761840-93761841	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs146581511	chr4:93762027-93762028	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs181273035	chr4:93762058-93762059	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs534107212	chr4:93762063-93762064	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs542178988	chr4:93762082-93762083	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs139547544	chr4:93762097-93762098	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs149719509	chr4:93762114-93762115	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs184104149	chr4:93762119-93762120	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs564215468	chr4:93762165-93762166	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs189399882	chr4:93762178-93762179	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs181042674	chr4:93762186-93762187	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs559745971	chr4:93762212-93762213	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs528845906	chr4:93762214-93762215	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs549283403	chr4:93762292-93762293	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs76038300	chr4:93762307-93762308	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs537571895	chr4:93762311-93762312	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs531937481	chr4:93762337-93762338	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs187378088	chr4:93762377-93762378	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs554679116	chr4:93762388-93762389	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs534059863	chr4:93762410-93762411	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs145588757	chr4:93762424-93762425	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs567677885	chr4:93762485-93762486	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs114769936	chr4:93762502-93762503	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs555701647	chr4:93762512-93762513	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs17326038	chr4:93762550-93762551	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs544488655	chr4:93762551-93762552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557716944	chr4:93762552-93762553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577748808	chr4:93762582-93762583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541861596	chr4:93762614-93762615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539976152	chr4:93762615-93762616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190402880	chr4:93762630-93762631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181633684	chr4:93762683-93762684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs148899794	chr4:93762705-93762706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563244703	chr4:93762756-93762757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563206474	chr4:93762771-93762772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370078432	chr4:93762781-93762782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186157340	chr4:93762850-93762851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs147018470	chr4:93762851-93762852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565372091	chr4:93762884-93762885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190744396	chr4:93762886-93762887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147555652	chr4:93762902-93762903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182618258	chr4:93762916-93762917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536654555	chr4:93762925-93762926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553781286	chr4:93762942-93762943	Weak transcription Enhancers	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
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
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	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
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Autism	20841430	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:206 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:93758200-93802200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr4:93758400-93764200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:93759800-93767400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:93762400-93764000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:93764000-93766000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:93766000-93767000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:93767000-93767400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:93767200-93768000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr4:93767200-93768000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:93767400-93768400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:93767400-93768600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:93767400-93768600	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr4:93767600-93768400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr4:93767800-93768400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:93767800-93768600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:93767800-93768600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr4:93768000-93768600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr4:93768400-93769200	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr4:93768400-93773400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr4:93768600-93769200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:93768600-93773000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr4:93768600-93773400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr4:93769200-93769400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr4:93769200-93770000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:93769400-93785000	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr4:93770000-93772800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:93772800-93773400	Enhancers	Fetal Intestine Small	intestine
28	chr4:93772800-93774400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:93773000-93773800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr4:93773200-93773800	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr4:93773400-93773600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr4:93773400-93773800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:93773600-93774200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr4:93773800-93783000	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr4:93777200-93786800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr4:93783000-93787400	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr4:93783800-93784600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr4:93784000-93788000	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr4:93784600-93785600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr4:93785000-93786000	Strong transcription	HUES48 Cell Line	embryonic stem cell
41	chr4:93785200-93785800	Enhancers	Brain Germinal Matrix	brain
42	chr4:93785200-93786000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:93785600-93785800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr4:93785800-93788400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr4:93786000-93800600	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr4:93787400-93788600	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr4:93788400-93788600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr4:93788600-93788800	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr4:93793600-93793800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr4:93793800-93794000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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