Variant report

Variant	nsv537194
Chromosome Location	chr4:98529206-98841438
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:802)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:98607042-98607171	K562	blood:	n/a	n/a
2	BACH1	chr4:98577260-98577434	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:98831268-98831463	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr4:98618600-98618916	K562	blood:	n/a	n/a
5	CEBPB	chr4:98577196-98577821	HepG2	liver:	n/a	n/a
6	CEBPB	chr4:98577169-98577759	HCT-116	colon:	n/a	n/a
7	CEBPB	chr4:98693338-98693594	HepG2	liver:	n/a	chr4:98693506-98693515 chr4:98693443-98693456
8	CEBPB	chr4:98539500-98539574	H1-hESC	embryonic stem cell:	n/a	chr4:98539512-98539523
9	CEBPB	chr4:98664347-98664413	K562	blood:	n/a	chr4:98664382-98664393
10	CEBPB	chr4:98748818-98748844	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr4:98586371-98586560	HepG2	liver:	n/a	chr4:98586497-98586508
12	CEBPB	chr4:98577187-98577805	A549	lung:	n/a	n/a
13	CEBPB	chr4:98577269-98577808	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr4:98664241-98664530	HepG2	liver:	n/a	chr4:98664382-98664393
15	CEBPB	chr4:98675730-98675981	HepG2	liver:	n/a	chr4:98675830-98675841
16	CEBPB	chr4:98577159-98577857	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:98778897-98779215	HepG2	liver:	n/a	chr4:98779056-98779067
18	CEBPB	chr4:98539434-98539658	HepG2	liver:	n/a	chr4:98539512-98539523
19	CEBPB	chr4:98581138-98581275	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr4:98577090-98577696	HCT-116	colon:	n/a	n/a
21	CEBPB	chr4:98778907-98779234	IMR90	lung:	n/a	chr4:98779056-98779067
22	CEBPB	chr4:98577066-98577631	MCF-7	breast:	n/a	n/a
23	CEBPB	chr4:98664215-98664532	IMR90	lung:	n/a	chr4:98664382-98664393
24	CEBPB	chr4:98577212-98577826	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:98577188-98577535	A549	lung:	n/a	n/a
26	CEBPB	chr4:98550616-98550860	A549	lung:	n/a	n/a
27	CEBPB	chr4:98832733-98832877	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr4:98577590-98577861	MCF-7	breast:	n/a	n/a
29	CEBPB	chr4:98577086-98577649	A549	lung:	n/a	n/a
30	CEBPB	chr4:98668425-98668529	A549	lung:	n/a	n/a
31	CEBPB	chr4:98577095-98577574	MCF-7	breast:	n/a	n/a
32	CEBPB	chr4:98650603-98650914	HepG2	liver:	n/a	chr4:98650742-98650753 chr4:98650740-98650751 chr4:98650742-98650751
33	CEBPB	chr4:98646521-98646790	HepG2	liver:	n/a	chr4:98646627-98646638
34	CEBPB	chr4:98795872-98796026	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:98551808-98552192	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr4:98650615-98650904	IMR90	lung:	n/a	chr4:98650742-98650753 chr4:98650740-98650751 chr4:98650742-98650751
37	CEBPB	chr4:98684928-98685150	HepG2	liver:	n/a	chr4:98685036-98685049 chr4:98685038-98685049 chr4:98684997-98685010 chr4:98685036-98685047
38	CEBPB	chr4:98778997-98779197	K562	blood:	n/a	chr4:98779056-98779067
39	CEBPB	chr4:98649287-98649587	HepG2	liver:	n/a	chr4:98649425-98649436 chr4:98649425-98649434
40	CEBPB	chr4:98550602-98550799	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:98586380-98586651	IMR90	lung:	n/a	chr4:98586497-98586508
42	CEBPB	chr4:98766860-98767235	H1-hESC	embryonic stem cell:	n/a	chr4:98767092-98767109
43	CEBPB	chr4:98664377-98664429	H1-hESC	embryonic stem cell:	n/a	chr4:98664382-98664393
44	CTCF	chr4:98613283-98613325	GM20000	blood:	n/a	n/a
45	CTCF	chr4:98831287-98831377	SK-N-SH_RA	brain:	n/a	chr4:98831342-98831355
46	CTCF	chr4:98837791-98837871	Fibrobl	skin:	n/a	n/a
47	CTCF	chr4:98642020-98642170	RPTEC	kidney:	n/a	n/a
48	CTCF	chr4:98831200-98831350	BE2_C	brain:	n/a	n/a
49	CTCF	chr4:98831240-98831390	GM12865	blood:	n/a	chr4:98831342-98831355
50	CTCF	chr4:98642360-98642510	SAEC	small airway:	n/a	chr4:98642420-98642436 chr4:98642419-98642437 chr4:98642414-98642435

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:98690072-98690122	HCT-116	colon:	n/a
2	chr4:98690072-98690122	HCM	heart:	n/a
3	chr4:98690072-98690122	BE2_C	brain:	n/a
4	chr4:98690072-98690122	AG10803	skin:	n/a
5	chr4:98690072-98690122	RPTEC	kidney:	n/a
6	chr4:98690072-98690122	NHDF-neo	bronchial:	n/a
7	chr4:98690072-98690122	HNPCEpiC	eye:	n/a
8	chr4:98690072-98690122	ovcar-3	ovarian:	n/a
9	chr4:98690072-98690122	GM12892	blood:	n/a
10	chr4:98690072-98690122	AG09309	skin:	n/a
11	chr4:98690072-98690122	HL-60	blood:	n/a
12	chr4:98690072-98690122	CMK	blood:	n/a
13	chr4:98690072-98690122	AG04449	skin:	fetal
14	chr4:98690072-98690122	LNCaP	prostate:	n/a
15	chr4:98690072-98690122	NB4	blood:	n/a
16	chr4:98690072-98690122	HEK293	kidney:	embryo
17	chr4:98690072-98690122	HRE	kidney:	n/a
18	chr4:98690072-98690122	GM06990	blood:	n/a
19	chr4:98690072-98690122	HUVEC	blood vessel:	n/a
20	chr4:98690072-98690122	U87	brain:	n/a
21	chr4:98690072-98690122	HRPEpiC	eye:	n/a
22	chr4:98690072-98690122	AG09319	gingival:	n/a
23	chr4:98690072-98690122	GM12891	blood:	n/a
24	chr4:98690072-98690122	PANC-1	pancreas:	n/a
25	chr4:98690072-98690122	MCF10A-Er-Src	breast:	n/a
26	chr4:98690072-98690122	Hela-S3	cervix:	n/a
27	chr4:98690072-98690122	HepG2	liver:	n/a
28	chr4:98690072-98690122	A549	lung:	n/a
29	chr4:98690072-98690122	HEEpiC	esophagus:	n/a
30	chr4:98690072-98690122	SKMC	muscle:	n/a
31	chr4:98690072-98690122	T-47D	breast:	n/a
32	chr4:98690072-98690122	ECC-1	luminal epithelium:	n/a
33	chr4:98690072-98690122	HIPEpiC	eye:	n/a
34	chr4:98690072-98690122	NH-A	brain:	n/a
35	chr4:98690072-98690122	HRCEpiC	kidney:	n/a
36	chr4:98690072-98690122	Jurkat	blood:	n/a
37	chr4:98690072-98690122	PFSK-1	brain:	n/a
38	chr4:98690072-98690122	GM19239	blood:	n/a
39	chr4:98690072-98690122	BJ	skin:	n/a
40	chr4:98690072-98690122	SK-N-MC	brain:	n/a
41	chr4:98690072-98690122	MCF-7	breast:	n/a
42	chr4:98690072-98690122	Hepatocyte	liver:	n/a
43	chr4:98690072-98690122	PrEC	prostate:	n/a
44	chr4:98690072-98690122	AoSMC	blood vessel:	n/a
45	chr4:98690072-98690122	HAEpiC	amniotic membrane:	n/a
46	chr4:98690072-98690122	Caco-2	colon:	n/a
47	chr4:98690072-98690122	HCF	heart:	n/a
48	chr4:98690072-98690122	HMEC	breast:	n/a
49	chr4:98690072-98690122	SAEC	small airway:	n/a
50	chr4:98690072-98690122	IMR90	lung:	fetal

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:98576156..98578566-chr4:98579040..98581603,2	MCF-7	breast:
2	chr4:98547951..98550382-chr4:98550750..98552792,2	MCF-7	breast:
3	chr4:98522959..98525428-chr4:98528956..98531903,2	K562	blood:
4	chr4:98600978..98604672-chr4:98609268..98612042,3	MCF-7	breast:
5	chr4:98790810..98793729-chr4:98795373..98798047,2	K562	blood:
6	chr4:98576156..98578566-chr4:98579040..98581603,2	MCF-7	breast:
7	chr4:98687863..98690416-chr4:98692655..98695152,2	MCF-7	breast:
8	chr4:98562115..98565020-chr4:98567699..98570313,2	MCF-7	breast:
9	chr4:98600978..98604672-chr4:98609268..98612042,3	MCF-7	breast:
10	chr4:98562115..98565020-chr4:98567699..98570313,2	MCF-7	breast:
11	chr4:97091475..97092009-chr4:98641981..98642501,2	MCF-7	breast:
12	chr4:98687863..98690416-chr4:98692655..98695152,2	MCF-7	breast:
13	chr4:98588787..98591250-chr4:98592135..98594195,2	MCF-7	breast:
14	chr4:98588787..98591250-chr4:98592135..98594195,2	MCF-7	breast:
15	chr4:98547951..98550382-chr4:98550750..98552792,2	MCF-7	breast:
16	chr4:98765331..98767165-chr4:99012892..99015543,2	K562	blood:
17	chr4:98641928..98642827-chr4:98905748..98906362,2	MCF-7	breast:
18	chr4:98790810..98793729-chr4:98795373..98798047,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN5-3	chr4:98814203-98814354	NONHSAT097477
2	lnc-TSPAN5-3	chr4:98633850-98633965	NONHSAT097477

No data

Variant related genes	Relation type
STPG2	TF binding region
CRYZP2	TF binding region
ENSG00000254044	TF binding region
STPG2	CpG island
CRYZP2	CpG island
ENSG00000254044	CpG island

Extended variants
information (count: 3859 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3859 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143461332	chr4:98548614-98548615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs570055418	chr4:98548634-98548635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537759905	chr4:98548661-98548662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150927877	chr4:98548694-98548695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574198598	chr4:98548707-98548708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541529945	chr4:98548760-98548761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552489849	chr4:98548768-98548769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs377358203	chr4:98548880-98548881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553870076	chr4:98548937-98548938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572051045	chr4:98548951-98548952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545860214	chr4:98548962-98548963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570804208	chr4:98549011-98549012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113721324	chr4:98549012-98549013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564361960	chr4:98549027-98549028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531593241	chr4:98549037-98549038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183958624	chr4:98549074-98549075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140667815	chr4:98549080-98549081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529101603	chr4:98549114-98549115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559299132	chr4:98549131-98549132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187788725	chr4:98549145-98549146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs111608626	chr4:98549146-98549147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565863080	chr4:98549175-98549176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150119555	chr4:98549190-98549191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551322181	chr4:98549191-98549192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113386471	chr4:98549218-98549219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569718042	chr4:98549230-98549231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115193665	chr4:98549240-98549241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138696028	chr4:98549271-98549272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567746846	chr4:98549289-98549290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192927153	chr4:98549295-98549296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115727694	chr4:98549301-98549302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144000286	chr4:98549344-98549345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1508475	chr4:98549362-98549363	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs79294424	chr4:98549415-98549416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576007004	chr4:98549427-98549428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545434296	chr4:98549430-98549431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543317142	chr4:98549463-98549464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201468119	chr4:98549479-98549480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562050167	chr4:98549486-98549487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529055152	chr4:98549533-98549534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185025646	chr4:98549544-98549545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559132257	chr4:98549566-98549567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146748444	chr4:98549615-98549616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190312953	chr4:98549646-98549647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535898612	chr4:98549701-98549702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371433503	chr4:98549817-98549818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111861286	chr4:98549829-98549830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569681162	chr4:98549855-98549856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113633925	chr4:98549856-98549857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549392516	chr4:98549880-98549881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Gastric cancer	16891809	CNVD

Chromatin state (count:229 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98548600-98549400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:98548800-98549200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:98548800-98549400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr4:98548800-98549400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:98549200-98549400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr4:98549400-98552800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr4:98551600-98552800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr4:98552800-98553000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr4:98552800-98553000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr4:98553000-98553800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr4:98553000-98554000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr4:98553800-98554800	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr4:98553800-98555400	Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr4:98554000-98554200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr4:98554200-98554800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr4:98554200-98555000	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr4:98564000-98564600	Enhancers	NHEK	skin
18	chr4:98564000-98564800	Enhancers	HUVEC	blood vessel
19	chr4:98564000-98565000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:98565600-98565800	Enhancers	Fetal Lung	lung
21	chr4:98565800-98566400	Weak transcription	Fetal Lung	lung
22	chr4:98566000-98567000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr4:98566000-98567200	Enhancers	Colon Smooth Muscle	Colon
24	chr4:98566400-98567200	Enhancers	Fetal Lung	lung
25	chr4:98566600-98567000	Enhancers	Fetal Heart	heart
26	chr4:98566600-98567200	Enhancers	Fetal Muscle Leg	muscle
27	chr4:98567200-98568200	Weak transcription	Colon Smooth Muscle	Colon
28	chr4:98567200-98568800	Weak transcription	Fetal Muscle Leg	muscle
29	chr4:98568200-98568800	Enhancers	Colon Smooth Muscle	Colon
30	chr4:98568400-98569000	Enhancers	Fetal Brain Female	brain
31	chr4:98568400-98569000	Enhancers	Fetal Stomach	stomach
32	chr4:98568400-98569000	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr4:98568600-98569200	Enhancers	Psoas Muscle	Psoas
34	chr4:98568800-98569400	Enhancers	Fetal Muscle Leg	muscle
35	chr4:98572800-98573200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:98573200-98574200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:98574200-98574400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:98574400-98574800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:98574800-98575200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:98574800-98575200	Enhancers	Placenta Amnion	Placenta Amnion
41	chr4:98575000-98575200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:98575200-98585200	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr4:98575400-98577600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:98576200-98577800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr4:98576400-98577800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:98576400-98577800	Enhancers	NHEK	skin
47	chr4:98576600-98577800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:98576600-98577800	Enhancers	HMEC	breast
49	chr4:98576800-98577600	Enhancers	A549	lung
50	chr4:98576800-98577800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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