Variant report

Variant	nsv830014
Chromosome Location	chr4:98220259-98419635
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	BCL11A	chr4:98238883-98239108	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr4:98288912-98289522	HCT-116	colon:	n/a	n/a
3	CBX3	chr4:98417471-98418225	HCT-116	colon:	n/a	n/a
4	CBX3	chr4:98288837-98289503	HCT-116	colon:	n/a	n/a
5	CBX3	chr4:98315840-98316257	HCT-116	colon:	n/a	n/a
6	CCNT2	chr4:98239443-98239649	K562	blood:	n/a	n/a
7	CCNT2	chr4:98381841-98382041	K562	blood:	n/a	n/a
8	CEBPB	chr4:98230429-98230673	A549	lung:	n/a	chr4:98230611-98230620 chr4:98230609-98230622 chr4:98230609-98230620
9	CEBPB	chr4:98334349-98334609	HepG2	liver:	n/a	chr4:98334483-98334494
10	CEBPB	chr4:98361102-98361428	HepG2	liver:	n/a	chr4:98361251-98361262 chr4:98361144-98361157
11	CEBPB	chr4:98417536-98417949	A549	lung:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
12	CEBPB	chr4:98417396-98418127	HCT-116	colon:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
13	CEBPB	chr4:98288913-98289569	HCT-116	colon:	n/a	n/a
14	CEBPB	chr4:98361249-98361274	H1-hESC	embryonic stem cell:	n/a	chr4:98361251-98361262
15	CEBPB	chr4:98400579-98400890	HepG2	liver:	n/a	chr4:98400705-98400714 chr4:98400705-98400714 chr4:98400705-98400714 chr4:98400583-98400596 chr4:98400703-98400714 chr4:98400705-98400714 chr4:98400703-98400716
16	CEBPB	chr4:98357248-98357445	IMR90	lung:	n/a	chr4:98357275-98357292
17	CEBPB	chr4:98378325-98378734	MCF-7	breast:	n/a	n/a
18	CEBPB	chr4:98415901-98416161	A549	lung:	n/a	chr4:98416021-98416032 chr4:98416020-98416033
19	CEBPB	chr4:98287697-98287967	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr4:98400558-98400870	IMR90	lung:	n/a	chr4:98400705-98400714 chr4:98400705-98400714 chr4:98400705-98400714 chr4:98400583-98400596 chr4:98400703-98400714 chr4:98400705-98400714 chr4:98400703-98400716
21	CEBPB	chr4:98361205-98361386	A549	lung:	n/a	chr4:98361251-98361262
22	CEBPB	chr4:98282274-98282599	HepG2	liver:	n/a	chr4:98282454-98282463 chr4:98282452-98282463
23	CEBPB	chr4:98417464-98417940	ECC-1	luminal epithelium:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
24	CEBPB	chr4:98415862-98416120	HepG2	liver:	n/a	chr4:98416021-98416032 chr4:98416020-98416033
25	CEBPB	chr4:98417526-98417894	H1-hESC	embryonic stem cell:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
26	CEBPB	chr4:98266170-98266331	K562	blood:	n/a	chr4:98266303-98266314
27	CEBPB	chr4:98313030-98313230	HepG2	liver:	n/a	chr4:98313089-98313100 chr4:98313091-98313100 chr4:98313090-98313101
28	CEBPB	chr4:98357227-98357418	A549	lung:	n/a	chr4:98357275-98357292
29	CEBPB	chr4:98266279-98266403	HepG2	liver:	n/a	chr4:98266303-98266314
30	CEBPB	chr4:98417519-98417952	A549	lung:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
31	CEBPB	chr4:98417537-98418092	Hela-S3	cervix:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
32	CEBPB	chr4:98417488-98417912	ECC-1	luminal epithelium:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
33	CEBPB	chr4:98417419-98418098	A549	lung:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
34	CTCF	chr4:98359798-98359876	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:98378700-98378850	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:98221878-98221973	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:98221840-98221990	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr4:98359760-98359910	HMEC	breast:	n/a	n/a
39	CTCF	chr4:98333449-98333505	GM13976	blood:	n/a	n/a
40	CTCF	chr4:98359760-98359910	SAEC	small airway:	n/a	n/a
41	CTCF	chr4:98378602-98378792	LNCaP	prostate:	n/a	n/a
42	CTCF	chr4:98314373-98314439	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr4:98378480-98378630	HRE	kidney:	n/a	n/a
44	CTCF	chr4:98359711-98359982	GM12878	blood:	n/a	n/a
45	CTCF	chr4:98359851-98359901	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr4:98359787-98359836	A549	lung:	n/a	n/a
47	CTCF	chr4:98301115-98301148	GM10248	blood:	n/a	n/a
48	CTCF	chr4:98359808-98359832	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:98246555-98246646	GM20000	blood:	n/a	n/a
50	CTCF	chr4:98221820-98221970	WERI-Rb-1	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:98270564-98270614	SK-N-SH	brain:	n/a
2	chr4:98239185-98239235	AG10803	skin:	n/a
3	chr4:98239185-98239235	AG09309	skin:	n/a
4	chr4:98270564-98270614	HRCEpiC	kidney:	n/a
5	chr4:98239185-98239235	SAEC	small airway:	n/a
6	chr4:98239185-98239235	ECC-1	luminal epithelium:	n/a
7	chr4:98270564-98270614	AG04450	lung:	fetal
8	chr4:98239185-98239235	Hela-S3	cervix:	n/a
9	chr4:98270564-98270614	Caco-2	colon:	n/a
10	chr4:98239185-98239235	HAEpiC	amniotic membrane:	n/a
11	chr4:98270564-98270614	PFSK-1	brain:	n/a
12	chr4:98270564-98270614	ECC-1	luminal epithelium:	n/a
13	chr4:98270564-98270614	LNCaP	prostate:	n/a
14	chr4:98239185-98239235	SK-N-SH	brain:	n/a
15	chr4:98270564-98270614	GM12892	blood:	n/a
16	chr4:98270564-98270614	K562	blood:	n/a
17	chr4:98270564-98270614	SAEC	small airway:	n/a
18	chr4:98239185-98239235	HRE	kidney:	n/a
19	chr4:98239185-98239235	SK-N-MC	brain:	n/a
20	chr4:98239185-98239235	RPTEC	kidney:	n/a
21	chr4:98239185-98239235	HRCEpiC	kidney:	n/a
22	chr4:98239185-98239235	PFSK-1	brain:	n/a
23	chr4:98239185-98239235	HRPEpiC	eye:	n/a
24	chr4:98270564-98270614	AG09319	gingival:	n/a
25	chr4:98270564-98270614	GM12878	blood:	n/a
26	chr4:98270564-98270614	HNPCEpiC	eye:	n/a
27	chr4:98239185-98239235	T-47D	breast:	n/a
28	chr4:98239185-98239235	BE2_C	brain:	n/a
29	chr4:98239185-98239235	HCM	heart:	n/a
30	chr4:98239185-98239235	IMR90	lung:	fetal
31	chr4:98270564-98270614	HAEpiC	amniotic membrane:	n/a
32	chr4:98270564-98270614	T-47D	breast:	n/a
33	chr4:98239185-98239235	AoSMC	blood vessel:	n/a
34	chr4:98239185-98239235	AG09319	gingival:	n/a
35	chr4:98270564-98270614	ProgFib	skin:	n/a
36	chr4:98270564-98270614	BJ	skin:	n/a
37	chr4:98239185-98239235	ProgFib	skin:	n/a
38	chr4:98270564-98270614	RPTEC	kidney:	n/a
39	chr4:98239185-98239235	ovcar-3	ovarian:	n/a
40	chr4:98239185-98239235	HepG2	liver:	n/a
41	chr4:98270564-98270614	PrEC	prostate:	n/a
42	chr4:98270564-98270614	Hepatocyte	liver:	n/a
43	chr4:98270564-98270614	A549	lung:	n/a
44	chr4:98270564-98270614	GM06990	blood:	n/a
45	chr4:98270564-98270614	HCM	heart:	n/a
46	chr4:98239185-98239235	HL-60	blood:	n/a
47	chr4:98239185-98239235	GM19239	blood:	n/a
48	chr4:98239185-98239235	HEEpiC	esophagus:	n/a
49	chr4:98239185-98239235	HPAEpiC	pulmonary alveolar:	n/a
50	chr4:98239185-98239235	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:98392071..98393852-chr4:98399439..98402050,2	K562	blood:
2	chr4:98392071..98393852-chr4:98399439..98402050,2	K562	blood:
3	chr4:98272027..98274172-chr4:98281216..98283718,2	K562	blood:
4	chr4:98123649..98126373-chr4:98396261..98399179,2	MCF-7	breast:
5	chr4:98417634..98419230-chr4:98419373..98421465,2	MCF-7	breast:
6	chr4:98356561..98358101-chr4:98363641..98366238,2	MCF-7	breast:
7	chr4:98250111..98251709-chr4:98255056..98256606,2	MCF-7	breast:
8	chr4:98417634..98419230-chr4:98419373..98421465,2	MCF-7	breast:
9	chr4:98250111..98251709-chr4:98255056..98256606,2	MCF-7	breast:
10	chr4:98401691..98403419-chr4:98441466..98443377,2	K562	blood:
11	chr4:98326975..98329466-chr4:98330567..98333090,2	MCF-7	breast:
12	chr4:98272027..98274172-chr4:98281216..98283718,2	K562	blood:
13	chr4:98326975..98329466-chr4:98330567..98333090,2	MCF-7	breast:
14	chr4:98356561..98358101-chr4:98363641..98366238,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAP1GDS1-4	chr4:98410925-98410963	ENSG00000251620.1
2	lnc-RAP1GDS1-4	chr4:98411147-98411315	ENSG00000251620.1
3	lnc-RAP1GDS1-4	chr4:98360505-98360572	ENSG00000251620.1
4	lnc-RAP1GDS1-4	chr4:98362561-98362710	ENSG00000251620.1
5	lnc-RAP1GDS1-4	chr4:98288077-98288139	ENSG00000251620.1
6	lnc-RAP1GDS1-4	chr4:98384696-98384743	ENSG00000251620.1

Variant related genes	Relation type
ENSG00000271995	TF binding region
STPG2-AS1	TF binding region
ENSG00000271995	CpG island
STPG2-AS1	CpG island

Extended variants
information (count: 3374 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3374 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140696380	chr4:98236840-98236841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73831880	chr4:98236841-98236842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550432572	chr4:98236912-98236913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568809971	chr4:98236913-98236914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535887642	chr4:98236936-98236937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190459645	chr4:98236941-98236942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566777218	chr4:98236966-98236967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144708825	chr4:98236971-98236972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs527412723	chr4:98236991-98236992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558773436	chr4:98237048-98237049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576995622	chr4:98237055-98237056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34994439	chr4:98237086-98237087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1462778	chr4:98237090-98237091	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs556403451	chr4:98237103-98237104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs80142815	chr4:98237130-98237131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183475035	chr4:98237194-98237195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140773498	chr4:98237218-98237219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201042816	chr4:98237305-98237306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111339359	chr4:98237328-98237329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188863689	chr4:98237336-98237337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs72677817	chr4:98237349-98237350	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs564319502	chr4:98237358-98237359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531836063	chr4:98237382-98237383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544263583	chr4:98237489-98237490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201688863	chr4:98237498-98237499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562455110	chr4:98237502-98237503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200525660	chr4:98237503-98237504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201549430	chr4:98237507-98237508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201031550	chr4:98237508-98237509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34616926	chr4:98237509-98237510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201963450	chr4:98237512-98237513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372319443	chr4:98237514-98237515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397994628	chr4:98237524-98237525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113837080	chr4:98237526-98237527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192030981	chr4:98237527-98237528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141607843	chr4:98237543-98237544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374291030	chr4:98237549-98237550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145118122	chr4:98237555-98237556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552524929	chr4:98237621-98237622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368493015	chr4:98237644-98237645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78176378	chr4:98237646-98237647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184188921	chr4:98237742-98237743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74522660	chr4:98237759-98237760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559245734	chr4:98237762-98237763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554378636	chr4:98237813-98237814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73831881	chr4:98237867-98237868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568463523	chr4:98237887-98237888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572148488	chr4:98237888-98237889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553735111	chr4:98237903-98237904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572136449	chr4:98237953-98237954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	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
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
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD
Melanoma	20688739	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98236800-98237200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:98237200-98238200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:98237800-98239800	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr4:98238200-98238400	Enhancers	Fetal Brain Male	brain
5	chr4:98238200-98238600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr4:98238200-98239800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:98238200-98239800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr4:98238200-98239800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr4:98238200-98240000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:98238200-98240000	Enhancers	Brain Germinal Matrix	brain
11	chr4:98238400-98238600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr4:98238400-98239000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:98238400-98239600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:98238400-98239800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr4:98238600-98238800	Enhancers	Liver	Liver
16	chr4:98238600-98239000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr4:98238600-98239000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr4:98238600-98239200	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr4:98238600-98239600	Weak transcription	Fetal Brain Male	brain
20	chr4:98238600-98240000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr4:98238800-98239200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:98238800-98239800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr4:98239000-98239600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr4:98239000-98239600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr4:98239200-98239600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr4:98239400-98240200	Enhancers	Fetal Brain Female	brain
27	chr4:98239600-98240000	Enhancers	Fetal Brain Male	brain
28	chr4:98239800-98241200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:98240000-98242400	Weak transcription	Fetal Brain Male	brain
30	chr4:98241200-98241600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:98241600-98241800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:98241800-98242000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:98242000-98244200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:98246200-98247000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr4:98248200-98248400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:98248800-98250600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:98249800-98250200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr4:98258000-98258600	ZNF genes & repeats	Pancreas	Pancrea
39	chr4:98267800-98268200	Enhancers	Brain Germinal Matrix	brain
40	chr4:98268200-98269800	Weak transcription	Brain Germinal Matrix	brain
41	chr4:98269400-98270200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:98269400-98271800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:98269600-98270000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr4:98269600-98271000	Enhancers	H1 Cell Line	embryonic stem cell
45	chr4:98269600-98271200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr4:98269600-98271400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:98269600-98271600	Enhancers	H9 Cell Line	embryonic stem cell
48	chr4:98269600-98271600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr4:98269800-98271400	Enhancers	Brain Germinal Matrix	brain
50	chr4:98269800-98271800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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