Variant report

Variant	nsv997640
Chromosome Location	chr4:93790604-93982695
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	chr4:93891228-93891471	A549	lung:	n/a	n/a
4	ATF3	chr4:93891072-93891445	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	chr4:93866144-93866453	HepG2	liver:	n/a	chr4:93866274-93866283 chr4:93866272-93866283
14	CEBPB	chr4:93835580-93835776	HepG2	liver:	n/a	chr4:93835654-93835665
15	CEBPB	chr4:93796324-93796523	HepG2	liver:	n/a	chr4:93796369-93796380
16	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
17	CEBPB	chr4:93901011-93901535	MCF-7	breast:	n/a	chr4:93901280-93901291
18	CEBPB	chr4:93964423-93964664	IMR90	lung:	n/a	chr4:93964542-93964553
19	CEBPB	chr4:93891027-93891542	MCF-7	breast:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
20	CEBPB	chr4:93890904-93891675	A549	lung:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
21	CEBPB	chr4:93965238-93965547	K562	blood:	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
22	CEBPB	chr4:93915947-93916152	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:93909578-93909840	H1-hESC	embryonic stem cell:	n/a	chr4:93909702-93909713 chr4:93909783-93909794
24	CEBPB	chr4:93891004-93891504	ECC-1	luminal epithelium:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
25	CEBPB	chr4:93890872-93891520	HepG2	liver:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
26	CEBPB	chr4:93891006-93891527	ECC-1	luminal epithelium:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
27	CEBPB	chr4:93909470-93909870	A549	lung:	n/a	chr4:93909702-93909713 chr4:93909783-93909794
28	CEBPB	chr4:93916641-93916775	A549	lung:	n/a	n/a
29	CEBPB	chr4:93933534-93933802	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:93795845-93796108	HepG2	liver:	n/a	chr4:93795963-93795974
31	CEBPB	chr4:93909521-93909888	Hela-S3	cervix:	n/a	chr4:93909702-93909713 chr4:93909783-93909794
32	CEBPB	chr4:93890512-93891528	Hela-S3	cervix:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
33	CEBPB	chr4:93964448-93964712	HepG2	liver:	n/a	chr4:93964542-93964553
34	CEBPB	chr4:93795868-93796039	IMR90	lung:	n/a	chr4:93795963-93795974
35	CEBPB	chr4:93901111-93901430	IMR90	lung:	n/a	chr4:93901280-93901291
36	CEBPB	chr4:93873627-93873920	HepG2	liver:	n/a	chr4:93873803-93873814 chr4:93873761-93873772 chr4:93873801-93873812
37	CEBPB	chr4:93973306-93973627	IMR90	lung:	n/a	chr4:93973459-93973468 chr4:93973459-93973468 chr4:93973459-93973468
38	CEBPB	chr4:93982510-93982808	HepG2	liver:	n/a	chr4:93982658-93982669
39	CEBPB	chr4:93901178-93901344	K562	blood:	n/a	chr4:93901280-93901291
40	CEBPB	chr4:93891086-93891438	H1-hESC	embryonic stem cell:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
41	CEBPB	chr4:93891027-93891462	HCT-116	colon:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
42	CEBPB	chr4:93901112-93901404	HepG2	liver:	n/a	chr4:93901280-93901291
43	CEBPB	chr4:93973333-93973620	HepG2	liver:	n/a	chr4:93973459-93973468 chr4:93973459-93973468 chr4:93973459-93973468
44	CEBPB	chr4:93886193-93886419	HepG2	liver:	n/a	chr4:93886329-93886340
45	CEBPB	chr4:93891066-93891580	A549	lung:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
46	CEBPB	chr4:93915896-93916844	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:93909536-93909890	IMR90	lung:	n/a	chr4:93909702-93909713 chr4:93909783-93909794
48	CEBPB	chr4:93982600-93982828	A549	lung:	n/a	chr4:93982658-93982669
49	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
50	CEBPB	chr4:93847023-93847348	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:93930622-93930672	BJ	skin:	n/a
2	chr4:93930622-93930672	T-47D	breast:	n/a
3	chr4:93930622-93930672	MCF10A-Er-Src	breast:	n/a
4	chr4:93930622-93930672	NHDF-neo	bronchial:	n/a
5	chr4:93930622-93930672	HCF	heart:	n/a
6	chr4:93930622-93930672	Hela-S3	cervix:	n/a
7	chr4:93930622-93930672	ovcar-3	ovarian:	n/a
8	chr4:93930622-93930672	HNPCEpiC	eye:	n/a
9	chr4:93930622-93930672	HRPEpiC	eye:	n/a
10	chr4:93930622-93930672	BE2_C	brain:	n/a
11	chr4:93930622-93930672	RPTEC	kidney:	n/a
12	chr4:93930622-93930672	ECC-1	luminal epithelium:	n/a
13	chr4:93930622-93930672	AG04450	lung:	fetal
14	chr4:93930622-93930672	PFSK-1	brain:	n/a
15	chr4:93930622-93930672	HCT-116	colon:	n/a
16	chr4:93930622-93930672	HepG2	liver:	n/a
17	chr4:93930622-93930672	HEK293	kidney:	embryo
18	chr4:93930622-93930672	H1-hESC	embryonic stem cell:	embryo
19	chr4:93930622-93930672	SAEC	small airway:	n/a
20	chr4:93930622-93930672	CMK	blood:	n/a
21	chr4:93930622-93930672	K562	blood:	n/a
22	chr4:93930622-93930672	HAEpiC	amniotic membrane:	n/a
23	chr4:93930622-93930672	U87	brain:	n/a
24	chr4:93930622-93930672	NHBE	bronchial:	n/a
25	chr4:93930622-93930672	SK-N-SH_RA	brain:	n/a
26	chr4:93930622-93930672	AG04449	skin:	fetal
27	chr4:93930622-93930672	HRE	kidney:	n/a
28	chr4:93930622-93930672	HCM	heart:	n/a
29	chr4:93930622-93930672	GM12891	blood:	n/a
30	chr4:93930622-93930672	GM19239	blood:	n/a
31	chr4:93930622-93930672	HMEC	breast:	n/a
32	chr4:93930622-93930672	A549	lung:	n/a
33	chr4:93930622-93930672	AG10803	skin:	n/a
34	chr4:93930622-93930672	AG09319	gingival:	n/a
35	chr4:93930622-93930672	HUVEC	blood vessel:	n/a
36	chr4:93930622-93930672	NH-A	brain:	n/a
37	chr4:93930622-93930672	AoSMC	blood vessel:	n/a
38	chr4:93930622-93930672	AG09309	skin:	n/a
39	chr4:93930622-93930672	GM12892	blood:	n/a
40	chr4:93930622-93930672	NB4	blood:	n/a
41	chr4:93930622-93930672	NT2-D1	testis:	n/a
42	chr4:93930622-93930672	HCPEpiC	choroid plexus:	n/a
43	chr4:93930622-93930672	HL-60	blood:	n/a
44	chr4:93930622-93930672	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:93930622-93930672	ProgFib	skin:	n/a
46	chr4:93930622-93930672	GM12878	blood:	n/a
47	chr4:93930622-93930672	SK-N-SH	brain:	n/a
48	chr4:93930622-93930672	IMR90	lung:	fetal
49	chr4:93930622-93930672	SKMC	muscle:	n/a
50	chr4:93930622-93930672	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:93886231..93887821-chr4:93901908..93903959,2	K562	blood:
2	chr4:93968750..93971596-chr4:93971794..93974511,2	MCF-7	breast:
3	chr4:93968750..93971596-chr4:93971794..93974511,2	MCF-7	breast:
4	chr4:93886231..93887821-chr4:93901908..93903959,2	K562	blood:
5	chr4:93827426..93829042-chr4:93829198..93830745,2	K562	blood:
6	chr4:93908293..93911044-chr4:93911588..93914279,2	MCF-7	breast:
7	chr4:93970682..93973329-chr4:93973340..93974971,2	MCF-7	breast:
8	chr4:93827426..93829042-chr4:93829198..93830745,2	K562	blood:
9	chr4:93920911..93923301-chr4:93923626..93925669,2	MCF-7	breast:
10	chr4:93908293..93911044-chr4:93911588..93914279,2	MCF-7	breast:
11	chr4:93825096..93827296-chr4:93828128..93830318,2	K562	blood:
12	chr4:93825096..93827296-chr4:93828128..93830318,2	K562	blood:
13	chr4:93920911..93923301-chr4:93923626..93925669,2	MCF-7	breast:
14	chr4:93846312..93847841-chr4:93851226..93853929,2	K562	blood:
15	chr4:93922270..93924469-chr4:93926058..93927823,2	MCF-7	breast:
16	chr4:93922270..93924469-chr4:93926058..93927823,2	MCF-7	breast:
17	chr4:93970682..93973329-chr4:93973340..93974971,2	MCF-7	breast:
18	chr4:93757984..93759775-chr4:93817140..93819795,2	MCF-7	breast:
19	chr4:93846312..93847841-chr4:93851226..93853929,2	K562	blood:

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

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

Extended variants
information (count: 4515 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4515 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115690485	chr4:93790616-93790617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564893563	chr4:93790697-93790698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143582556	chr4:93790718-93790719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191246573	chr4:93790824-93790825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs151011284	chr4:93790898-93790899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs35587569	chr4:93790907-93790908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536944164	chr4:93791020-93791021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550118573	chr4:93791063-93791064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183839181	chr4:93791077-93791078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140906873	chr4:93791109-93791110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113039146	chr4:93791110-93791111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150085109	chr4:93791124-93791125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187768083	chr4:93791148-93791149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554541695	chr4:93791151-93791152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192588348	chr4:93791153-93791154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377238800	chr4:93791160-93791161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138408149	chr4:93791175-93791176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576155586	chr4:93791179-93791180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544139935	chr4:93791187-93791188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544775625	chr4:93791191-93791192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185665870	chr4:93791271-93791272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541485325	chr4:93791291-93791292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2033586	chr4:93791307-93791308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114895348	chr4:93791308-93791309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563556616	chr4:93791363-93791364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530865116	chr4:93791371-93791372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546015770	chr4:93791387-93791388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564225274	chr4:93791416-93791417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370794678	chr4:93791418-93791419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs386418118	chr4:93791419-93791420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547459576	chr4:93791466-93791467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190184265	chr4:93791482-93791483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181883733	chr4:93791483-93791484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547035895	chr4:93791485-93791486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142740136	chr4:93791518-93791519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562437525	chr4:93791535-93791536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146962345	chr4:93791550-93791551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2033587	chr4:93791571-93791572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs375446716	chr4:93791587-93791588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539256538	chr4:93791643-93791644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113921687	chr4:93791646-93791647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139206475	chr4:93791695-93791696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184690303	chr4:93791704-93791705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568483717	chr4:93791714-93791715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34489425	chr4:93791763-93791764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371556944	chr4:93791770-93791771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143092191	chr4:93791771-93791772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550595944	chr4:93791775-93791776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189603305	chr4:93791831-93791832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73837367	chr4:93791833-93791834	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:93758200-93802200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr4:93786000-93800600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr4:93793600-93793800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:93793800-93794000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:93793800-93794200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:93793800-93794200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:93798200-93798800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:93798800-93809600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr4:93800400-93800800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr4:93800600-93800800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:93802000-93802400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:93802200-93802400	Enhancers	H1 Cell Line	embryonic stem cell
13	chr4:93806000-93807400	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr4:93806400-93806800	Enhancers	Fetal Brain Male	brain
15	chr4:93806400-93807200	Enhancers	Liver	Liver
16	chr4:93806600-93807400	Enhancers	Adipose Nuclei	Adipose
17	chr4:93809600-93809800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr4:93818000-93818600	Enhancers	Liver	Liver
19	chr4:93821800-93822200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:93822200-93823200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:93823200-93823800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:93827400-93827800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr4:93827800-93829000	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr4:93843200-93843600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:93843600-93845800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr4:93845600-93846400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr4:93845600-93846600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr4:93845600-93846600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr4:93845600-93846600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr4:93845600-93846800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr4:93845800-93846200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr4:93845800-93846200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr4:93845800-93846200	Enhancers	H1 Cell Line	embryonic stem cell
34	chr4:93845800-93846400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr4:93845800-93846400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:93852000-93852400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr4:93864200-93866800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr4:93864400-93874200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr4:93865400-93865800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
40	chr4:93865800-93895400	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr4:93871200-93883400	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr4:93871400-93883200	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr4:93882200-93882400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr4:93882400-93883000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr4:93883000-93883600	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr4:93883200-93883600	Enhancers	Fetal Brain Male	brain
47	chr4:93883200-93883800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr4:93883200-93883800	Enhancers	Fetal Heart	heart
49	chr4:93883400-93883800	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr4:93883600-93884400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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