Variant report

Variant	nsv830016
Chromosome Location	chr4:98360907-98550751
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	ATF3	chr4:98419887-98420492	HCT-116	colon:	n/a	n/a
2	ATF3	chr4:98419975-98420488	HCT-116	colon:	n/a	n/a
3	BACH1	chr4:98420053-98420303	H1-hESC	embryonic stem cell:	n/a	chr4:98420142-98420156
4	BCL3	chr4:98508998-98509375	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:98421683-98421883	GM12878	blood:	n/a	n/a
6	CBX3	chr4:98419866-98420528	HCT-116	colon:	n/a	n/a
7	CBX3	chr4:98419861-98420515	HCT-116	colon:	n/a	n/a
8	CBX3	chr4:98417471-98418225	HCT-116	colon:	n/a	n/a
9	CCNT2	chr4:98381841-98382041	K562	blood:	n/a	n/a
10	CEBPB	chr4:98417396-98418127	HCT-116	colon:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
11	CEBPB	chr4:98550602-98550799	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr4:98419853-98420528	A549	lung:	n/a	n/a
13	CEBPB	chr4:98415901-98416161	A549	lung:	n/a	chr4:98416021-98416032 chr4:98416020-98416033
14	CEBPB	chr4:98419984-98420473	A549	lung:	n/a	n/a
15	CEBPB	chr4:98467950-98468187	HepG2	liver:	n/a	chr4:98468073-98468084
16	CEBPB	chr4:98539434-98539658	HepG2	liver:	n/a	chr4:98539512-98539523
17	CEBPB	chr4:98419795-98420651	HCT-116	colon:	n/a	n/a
18	CEBPB	chr4:98539500-98539574	H1-hESC	embryonic stem cell:	n/a	chr4:98539512-98539523
19	CEBPB	chr4:98420213-98420360	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr4:98426750-98427060	HepG2	liver:	n/a	chr4:98426906-98426915 chr4:98426904-98426915 chr4:98426905-98426916
21	CEBPB	chr4:98550616-98550860	A549	lung:	n/a	n/a
22	CEBPB	chr4:98361249-98361274	H1-hESC	embryonic stem cell:	n/a	chr4:98361251-98361262
23	CEBPB	chr4:98420047-98420415	MCF-7	breast:	n/a	n/a
24	CEBPB	chr4:98419946-98420588	HCT-116	colon:	n/a	n/a
25	CEBPB	chr4:98510992-98511342	MCF-7	breast:	n/a	n/a
26	CEBPB	chr4:98510925-98511719	MCF-7	breast:	n/a	n/a
27	CEBPB	chr4:98417464-98417940	ECC-1	luminal epithelium:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
28	CEBPB	chr4:98415862-98416120	HepG2	liver:	n/a	chr4:98416021-98416032 chr4:98416020-98416033
29	CEBPB	chr4:98503490-98503558	H1-hESC	embryonic stem cell:	n/a	chr4:98503500-98503511 chr4:98503499-98503512
30	CEBPB	chr4:98417536-98417949	A549	lung:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
31	CEBPB	chr4:98361102-98361428	HepG2	liver:	n/a	chr4:98361251-98361262 chr4:98361144-98361157
32	CEBPB	chr4:98503368-98503620	HepG2	liver:	n/a	chr4:98503500-98503511 chr4:98503499-98503512
33	CEBPB	chr4:98361205-98361386	A549	lung:	n/a	chr4:98361251-98361262
34	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
35	CEBPB	chr4:98417519-98417952	A549	lung:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
36	CEBPB	chr4:98417419-98418098	A549	lung:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
37	CEBPB	chr4:98420044-98420447	MCF-7	breast:	n/a	n/a
38	CEBPB	chr4:98378325-98378734	MCF-7	breast:	n/a	n/a
39	CEBPB	chr4:98417537-98418092	Hela-S3	cervix:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
40	CEBPB	chr4:98417526-98417894	H1-hESC	embryonic stem cell:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
41	CEBPB	chr4:98419955-98420451	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr4:98467897-98468197	IMR90	lung:	n/a	chr4:98468073-98468084
43	CEBPB	chr4:98426805-98427085	A549	lung:	n/a	chr4:98426906-98426915 chr4:98426904-98426915 chr4:98426905-98426916
44	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
45	CEBPB	chr4:98420005-98420453	A549	lung:	n/a	n/a
46	CEBPB	chr4:98417488-98417912	ECC-1	luminal epithelium:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
47	CEBPB	chr4:98511464-98511776	MCF-7	breast:	n/a	n/a
48	CHD1	chr4:98522881-98522890	GM12878	blood:	n/a	n/a
49	CTCF	chr4:98470340-98470490	RPTEC	kidney:	n/a	n/a
50	CTCF	chr4:98528780-98528930	BE2_C	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:98479820-98479870	AG10803	skin:	n/a
2	chr4:98479820-98479870	NB4	blood:	n/a
3	chr4:98479820-98479870	ECC-1	luminal epithelium:	n/a
4	chr4:98479820-98479870	HCT-116	colon:	n/a
5	chr4:98479820-98479870	Hela-S3	cervix:	n/a
6	chr4:98479820-98479870	SK-N-SH	brain:	n/a
7	chr4:98479820-98479870	Jurkat	blood:	n/a
8	chr4:98479820-98479870	HCM	heart:	n/a
9	chr4:98479820-98479870	T-47D	breast:	n/a
10	chr4:98479820-98479870	Caco-2	colon:	n/a
11	chr4:98479820-98479870	HIPEpiC	eye:	n/a
12	chr4:98479820-98479870	PrEC	prostate:	n/a
13	chr4:98479820-98479870	K562	blood:	n/a
14	chr4:98479820-98479870	HL-60	blood:	n/a
15	chr4:98479820-98479870	HMEC	breast:	n/a
16	chr4:98479820-98479870	HRE	kidney:	n/a
17	chr4:98479820-98479870	HEK293	kidney:	embryo
18	chr4:98479820-98479870	AG09309	skin:	n/a
19	chr4:98479820-98479870	MCF10A-Er-Src	breast:	n/a
20	chr4:98479820-98479870	AG09319	gingival:	n/a
21	chr4:98479820-98479870	Hepatocyte	liver:	n/a
22	chr4:98479820-98479870	HNPCEpiC	eye:	n/a
23	chr4:98479820-98479870	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:98479820-98479870	A549	lung:	n/a
25	chr4:98479820-98479870	CMK	blood:	n/a
26	chr4:98479820-98479870	LNCaP	prostate:	n/a
27	chr4:98479820-98479870	ProgFib	skin:	n/a
28	chr4:98479820-98479870	NHDF-neo	bronchial:	n/a
29	chr4:98479820-98479870	H1-hESC	embryonic stem cell:	embryo
30	chr4:98479820-98479870	HCPEpiC	choroid plexus:	n/a
31	chr4:98479820-98479870	SK-N-MC	brain:	n/a
32	chr4:98479820-98479870	AG04450	lung:	fetal
33	chr4:98479820-98479870	SK-N-SH_RA	brain:	n/a
34	chr4:98479820-98479870	GM19239	blood:	n/a
35	chr4:98479820-98479870	GM12891	blood:	n/a
36	chr4:98479820-98479870	AG04449	skin:	fetal
37	chr4:98479820-98479870	BJ	skin:	n/a
38	chr4:98479820-98479870	U87	brain:	n/a
39	chr4:98479820-98479870	HUVEC	blood vessel:	n/a
40	chr4:98479820-98479870	AoSMC	blood vessel:	n/a
41	chr4:98479820-98479870	RPTEC	kidney:	n/a
42	chr4:98479820-98479870	HRPEpiC	eye:	n/a
43	chr4:98479820-98479870	HRCEpiC	kidney:	n/a
44	chr4:98479820-98479870	HCF	heart:	n/a
45	chr4:98479820-98479870	HAEpiC	amniotic membrane:	n/a
46	chr4:98479820-98479870	MCF-7	breast:	n/a
47	chr4:98479820-98479870	SKMC	muscle:	n/a
48	chr4:98479820-98479870	GM12892	blood:	n/a
49	chr4:98479820-98479870	NH-A	brain:	n/a
50	chr4:98479820-98479870	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:98505232..98506917-chr4:98508304..98511467,3	MCF-7	breast:
2	chr4:98356561..98358101-chr4:98363641..98366238,2	MCF-7	breast:
3	chr4:98522959..98525428-chr4:98528956..98531903,2	K562	blood:
4	chr4:98392071..98393852-chr4:98399439..98402050,2	K562	blood:
5	chr4:98392071..98393852-chr4:98399439..98402050,2	K562	blood:
6	chr4:98401691..98403419-chr4:98441466..98443377,2	K562	blood:
7	chr4:98547951..98550382-chr4:98550750..98552792,2	MCF-7	breast:
8	chr4:98417634..98419230-chr4:98419373..98421465,2	MCF-7	breast:
9	chr4:98522959..98525428-chr4:98528956..98531903,2	K562	blood:
10	chr4:98401691..98403419-chr4:98441466..98443377,2	K562	blood:
11	chr4:98417634..98419230-chr4:98419373..98421465,2	MCF-7	breast:
12	chr4:98505232..98506917-chr4:98508304..98511467,3	MCF-7	breast:
13	chr4:98547951..98550382-chr4:98550750..98552792,2	MCF-7	breast:
14	chr4:98123649..98126373-chr4:98396261..98399179,2	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	chr4:98384696-98384743	ENSG00000251620.1
4	lnc-RAP1GDS1-4	chr4:98362561-98362710	ENSG00000251620.1

Variant related genes	Relation type
ENSG00000271995	TF binding region
ENSG00000271995	CpG island

Extended variants
information (count: 3006 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3006 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547269773	chr4:98360953-98360954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533871903	chr4:98360964-98360965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191631289	chr4:98360980-98360981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183872674	chr4:98361072-98361073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146197295	chr4:98361112-98361113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1033131	chr4:98361136-98361137	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs139086508	chr4:98361158-98361159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536767650	chr4:98361184-98361185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555196728	chr4:98361185-98361186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567247710	chr4:98361206-98361207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534359409	chr4:98361213-98361214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187850883	chr4:98361216-98361217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76699549	chr4:98361233-98361234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545194137	chr4:98361259-98361260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557208279	chr4:98361279-98361280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575544628	chr4:98361286-98361287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543122852	chr4:98361327-98361328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537475143	chr4:98361331-98361332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192634824	chr4:98361333-98361334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528478569	chr4:98361338-98361339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540279794	chr4:98361351-98361352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565528697	chr4:98361371-98361372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372753982	chr4:98361429-98361430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150316668	chr4:98361435-98361436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1033130	chr4:98361476-98361477	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs376391218	chr4:98361486-98361487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556791185	chr4:98361498-98361499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530273574	chr4:98361521-98361522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77079878	chr4:98361522-98361523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567256653	chr4:98361538-98361539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78508483	chr4:98361546-98361547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144063386	chr4:98361568-98361569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553941151	chr4:98361593-98361594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150541318	chr4:98361613-98361614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557320732	chr4:98361676-98361677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs117693924	chr4:98361713-98361714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182122117	chr4:98361716-98361717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546913152	chr4:98361728-98361729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573262242	chr4:98361788-98361789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572343554	chr4:98361831-98361832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540595074	chr4:98361836-98361837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566483947	chr4:98361858-98361859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11942602	chr4:98361975-98361976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561251151	chr4:98362011-98362012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544498082	chr4:98362014-98362015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552632259	chr4:98362063-98362064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562881729	chr4:98362096-98362097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530190902	chr4:98362122-98362123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548498663	chr4:98362124-98362125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576357215	chr4:98362158-98362159	Weak transcription	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	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98359800-98368600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:98359800-98368600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:98368200-98369200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
4	chr4:98368600-98369000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:98368600-98369200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:98368600-98369200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:98369000-98369400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:98369200-98373400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:98369200-98374400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr4:98369400-98372200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:98372400-98374600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:98373000-98373400	ZNF genes & repeats	HSMM	muscle
13	chr4:98373400-98373600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr4:98373400-98374600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr4:98373400-98377800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr4:98374400-98374600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:98374400-98374600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr4:98374400-98374600	ZNF genes & repeats	Pancreas	Pancrea
19	chr4:98374600-98376400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:98374600-98378400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr4:98376400-98376600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:98377400-98378400	Enhancers	Liver	Liver
23	chr4:98377800-98378000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr4:98378200-98378400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr4:98378200-98379000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr4:98378200-98379000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr4:98378200-98379400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr4:98378400-98378600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr4:98378400-98378600	Flanking Active TSS	Liver	Liver
30	chr4:98378400-98379000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr4:98378400-98379000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr4:98378600-98378800	Enhancers	Liver	Liver
33	chr4:98378800-98379600	Flanking Active TSS	Liver	Liver
34	chr4:98378800-98379600	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr4:98379000-98379200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr4:98379000-98381200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr4:98379000-98382200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr4:98379400-98382200	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr4:98379600-98380000	Enhancers	Liver	Liver
40	chr4:98381200-98382600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr4:98382200-98382600	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr4:98382200-98382600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr4:98382200-98383000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr4:98382400-98382800	Enhancers	H9 Cell Line	embryonic stem cell
45	chr4:98383200-98386600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr4:98396600-98396800	Active TSS	Liver	Liver
47	chr4:98396800-98397000	Flanking Active TSS	Liver	Liver
48	chr4:98397000-98399000	Enhancers	Liver	Liver
49	chr4:98399000-98399200	Flanking Active TSS	Liver	Liver
50	chr4:98399200-98399400	Enhancers	Liver	Liver

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