Variant report

Variant	nsv879687
Chromosome Location	chr4:104288620-104371785
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:434)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:434 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:104345942-104346347	HepG2	liver:	n/a	n/a
2	ATF2	chr4:104350391-104350892	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:104350345-104350827	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:104321608-104321927	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr4:104350494-104350803	GM12878	blood:	n/a	n/a
6	BATF	chr4:104321623-104321858	GM12878	blood:	n/a	chr4:104321771-104321782
7	BHLHE40	chr4:104321687-104321948	K562	blood:	n/a	n/a
8	BHLHE40	chr4:104321736-104321854	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:104345952-104346257	HepG2	liver:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
10	CEBPB	chr4:104345926-104346419	H1-hESC	embryonic stem cell:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
11	CEBPB	chr4:104321803-104322048	HepG2	liver:	n/a	chr4:104321934-104321945
12	CEBPB	chr4:104328273-104328473	A549	lung:	n/a	chr4:104328385-104328396
13	CEBPB	chr4:104328268-104328562	HepG2	liver:	n/a	chr4:104328385-104328396
14	CEBPB	chr4:104345984-104346310	HepG2	liver:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
15	CEBPB	chr4:104366577-104366900	IMR90	lung:	n/a	chr4:104366712-104366723
16	CEBPB	chr4:104345795-104346680	MCF-7	breast:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
17	CEBPB	chr4:104361958-104362110	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:104345934-104346357	HepG2	liver:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
19	CEBPB	chr4:104366584-104366888	K562	blood:	n/a	chr4:104366712-104366723
20	CEBPB	chr4:104370810-104371129	HepG2	liver:	n/a	chr4:104370972-104370983
21	CEBPB	chr4:104350494-104351061	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:104370872-104371077	H1-hESC	embryonic stem cell:	n/a	chr4:104370972-104370983
23	CEBPB	chr4:104345847-104346459	A549	lung:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
24	CEBPB	chr4:104345859-104346453	MCF-7	breast:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
25	CEBPB	chr4:104345963-104346289	IMR90	lung:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
26	CEBPB	chr4:104345928-104346517	ECC-1	luminal epithelium:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
27	CEBPB	chr4:104345916-104346398	HepG2	liver:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
28	CEBPB	chr4:104346012-104346273	K562	blood:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
29	CEBPB	chr4:104345872-104346433	ECC-1	luminal epithelium:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
30	CEBPB	chr4:104366597-104366889	A549	lung:	n/a	chr4:104366712-104366723
31	CEBPB	chr4:104345945-104346358	A549	lung:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
32	CEBPB	chr4:104366530-104366878	HepG2	liver:	n/a	chr4:104366712-104366723
33	CEBPB	chr4:104345984-104346410	A549	lung:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
34	CEBPB	chr4:104345885-104346455	Hela-S3	cervix:	n/a	chr4:104346125-104346136 chr4:104346171-104346182
35	CEBPB	chr4:104366688-104366739	H1-hESC	embryonic stem cell:	n/a	chr4:104366712-104366723
36	CEBPD	chr4:104345980-104346328	HepG2	liver:	n/a	n/a
37	CHD2	chr4:104346035-104346344	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr4:104350482-104350877	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr4:104350476-104350824	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr4:104350381-104350884	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr4:104350341-104351208	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr4:104350520-104350670	NHEK	skin:	n/a	n/a
43	CTCF	chr4:104350600-104350750	BE2_C	brain:	n/a	n/a
44	CTCF	chr4:104350520-104350670	GM06990	blood:	n/a	n/a
45	CTCF	chr4:104350580-104350730	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr4:104336340-104336490	HepG2	liver:	n/a	n/a
47	CTCF	chr4:104336260-104336410	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:104350580-104350730	GM12865	blood:	n/a	n/a
49	CTCF	chr4:104350560-104350710	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr4:104350540-104350690	GM12864	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:104346019-104346069	SKMC	muscle:	n/a
2	chr4:104346019-104346069	IMR90	lung:	fetal
3	chr4:104346019-104346069	NHBE	bronchial:	n/a
4	chr4:104346019-104346069	GM12892	blood:	n/a
5	chr4:104346019-104346069	RPTEC	kidney:	n/a
6	chr4:104346019-104346069	AG09319	gingival:	n/a
7	chr4:104346019-104346069	SK-N-SH	brain:	n/a
8	chr4:104346019-104346069	NHDF-neo	bronchial:	n/a
9	chr4:104346019-104346069	HCPEpiC	choroid plexus:	n/a
10	chr4:104346019-104346069	GM12878	blood:	n/a
11	chr4:104346019-104346069	HAEpiC	amniotic membrane:	n/a
12	chr4:104346019-104346069	HCM	heart:	n/a
13	chr4:104346019-104346069	NT2-D1	testis:	n/a
14	chr4:104346019-104346069	H1-hESC	embryonic stem cell:	embryo
15	chr4:104346019-104346069	BE2_C	brain:	n/a
16	chr4:104346019-104346069	SK-N-SH_RA	brain:	n/a
17	chr4:104346019-104346069	ovcar-3	ovarian:	n/a
18	chr4:104346019-104346069	NB4	blood:	n/a
19	chr4:104346019-104346069	K562	blood:	n/a
20	chr4:104346019-104346069	HRE	kidney:	n/a
21	chr4:104346019-104346069	AoSMC	blood vessel:	n/a
22	chr4:104346019-104346069	HepG2	liver:	n/a
23	chr4:104346019-104346069	HUVEC	blood vessel:	n/a
24	chr4:104346019-104346069	Hela-S3	cervix:	n/a
25	chr4:104346019-104346069	LNCaP	prostate:	n/a
26	chr4:104346019-104346069	SAEC	small airway:	n/a
27	chr4:104346019-104346069	HMEC	breast:	n/a
28	chr4:104346019-104346069	ECC-1	luminal epithelium:	n/a
29	chr4:104346019-104346069	HIPEpiC	eye:	n/a
30	chr4:104346019-104346069	ProgFib	skin:	n/a
31	chr4:104346019-104346069	Jurkat	blood:	n/a
32	chr4:104346019-104346069	HCF	heart:	n/a
33	chr4:104346019-104346069	GM12891	blood:	n/a
34	chr4:104346019-104346069	AG04449	skin:	fetal
35	chr4:104346019-104346069	PFSK-1	brain:	n/a
36	chr4:104346019-104346069	BJ	skin:	n/a
37	chr4:104346019-104346069	A549	lung:	n/a
38	chr4:104346019-104346069	HRPEpiC	eye:	n/a
39	chr4:104346019-104346069	AG04450	lung:	fetal
40	chr4:104346019-104346069	HNPCEpiC	eye:	n/a
41	chr4:104346019-104346069	HEK293	kidney:	embryo
42	chr4:104346019-104346069	HEEpiC	esophagus:	n/a
43	chr4:104346019-104346069	MCF10A-Er-Src	breast:	n/a
44	chr4:104346019-104346069	HL-60	blood:	n/a
45	chr4:104346019-104346069	GM19239	blood:	n/a
46	chr4:104346019-104346069	PANC-1	pancreas:	n/a
47	chr4:104346019-104346069	Hepatocyte	liver:	n/a
48	chr4:104346019-104346069	GM06990	blood:	n/a
49	chr4:104346019-104346069	HCT-116	colon:	n/a
50	chr4:104346019-104346069	U87	brain:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:104322090..104323891-chr4:104326352..104329222,2	MCF-7	breast:
2	chr4:104322090..104323891-chr4:104326352..104329222,2	MCF-7	breast:
3	chr4:104333746..104335920-chr4:104344875..104346775,2	MCF-7	breast:
4	chr17:42276655..42278541-chr4:104366338..104369269,2	MCF-7	breast:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CISD2-3	chr4:104358092-104358203	ENSG00000248740
2	lnc-CISD2-3	chr4:104358874-104358999	NONHSAT097630
3	lnc-CISD2-3	chr4:104358092-104358203	ENSG00000248740
4	lnc-CISD2-3	chr4:104358875-104358999	ENSG00000248740
5	lnc-CISD2-3	chr4:104370248-104375195	NONHSAT097630
6	lnc-CISD2-3	chr4:104360782-104360885	XLOC_003629
7	lnc-CISD2-3	chr4:104346209-104346342	NONHSAT097632
8	lnc-CISD2-3	chr4:104346212-104346342	ENSG00000248740
9	lnc-CISD2-3	chr4:104358092-104358203	XLOC_003629
10	lnc-CISD2-3	chr4:104359861-104359920	XLOC_003629
11	lnc-CISD2-3	chr4:104360782-104360898	ENSG00000248740
12	lnc-CISD2-3	chr4:104358092-104358203	NONHSAT097632
13	lnc-CISD2-3	chr4:104360782-104360998	XLOC_003629
14	lnc-CISD2-3	chr4:104359860-104359920	NONHSAT097630
15	lnc-CISD2-3	chr4:104346199-104346342	XLOC_003629
16	lnc-CISD2-3	chr4:104346198-104346573	NONHSAT097630
17	lnc-CISD2-3	chr4:104358092-104358203	XLOC_003629
18	lnc-CISD2-3	chr4:104358084-104358203	NONHSAT097630
19	lnc-CISD2-3	chr4:104360781-104360998	NONHSAT097630
20	lnc-CISD2-3	chr4:104358875-104358999	XLOC_003629
21	lnc-CISD2-3	chr4:104346223-104346342	XLOC_003629
22	lnc-CISD2-3	chr4:104359864-104359920	XLOC_003629
23	lnc-CISD2-3	chr4:104358092-104358203	XLOC_003629
24	lnc-CISD2-3	chr4:104346223-104346342	XLOC_003629
25	lnc-CISD2-3	chr4:104346223-104346342	XLOC_003629
26	lnc-CISD2-3	chr4:104358092-104358203	XLOC_003629
27	lnc-CISD2-3	chr4:104298160-104298332	ENSG00000248740

No data

Variant related genes	Relation type
ENSG00000248740	TF binding region
ENSG00000248740	CpG island
ENSG00000087152	chromatin interactions
ENSG00000248740	chromatin interactions
EIF2C1	miRNA target sites

Extended variants
information (count: 2096 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2096 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11734572	chr4:104288620-104288621	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575696557	chr4:104288632-104288633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543098158	chr4:104288638-104288639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371158577	chr4:104288656-104288657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555062948	chr4:104288670-104288671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573279840	chr4:104288711-104288712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145439659	chr4:104288744-104288745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184622585	chr4:104288753-104288754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532412281	chr4:104288802-104288803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544123845	chr4:104288861-104288862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562690911	chr4:104288894-104288895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527240698	chr4:104288901-104288902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189238199	chr4:104288918-104288919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192393354	chr4:104288921-104288922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560981702	chr4:104288998-104288999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566202269	chr4:104289002-104289003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1022347	chr4:104289038-104289039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551739407	chr4:104289063-104289064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78880707	chr4:104289085-104289086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs111780873	chr4:104289130-104289131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79089134	chr4:104289180-104289181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371270033	chr4:104289188-104289189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs151307485	chr4:104289192-104289193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72952015	chr4:104289197-104289198	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs555126241	chr4:104289231-104289232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72952016	chr4:104289233-104289234	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs184728032	chr4:104289251-104289252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532022528	chr4:104289315-104289316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188792621	chr4:104289353-104289354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1400365	chr4:104289396-104289397	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs577102209	chr4:104289525-104289526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181684687	chr4:104289572-104289573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571082454	chr4:104289574-104289575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529920453	chr4:104289575-104289576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541590381	chr4:104289602-104289603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138339646	chr4:104289609-104289610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141270221	chr4:104289635-104289636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185370461	chr4:104289649-104289650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189971329	chr4:104289650-104289651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78363806	chr4:104289675-104289676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551262151	chr4:104289696-104289697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373964323	chr4:104289713-104289714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536854229	chr4:104289724-104289725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555187751	chr4:104289732-104289733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181326668	chr4:104289748-104289749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150194815	chr4:104289771-104289772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185964651	chr4:104289823-104289824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577168988	chr4:104289851-104289852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs74672721	chr4:104289861-104289862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139717238	chr4:104289869-104289870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
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
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	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
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:178 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:104282200-104293600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:104283800-104293200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:104283800-104296400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr4:104286400-104293400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr4:104286400-104293800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr4:104287000-104295000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr4:104291800-104292000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr4:104291800-104292000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr4:104291800-104292000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:104292000-104292200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr4:104292000-104293600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr4:104292000-104294000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr4:104292000-104295400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr4:104292200-104295200	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr4:104292800-104294200	Enhancers	HUVEC	blood vessel
16	chr4:104293200-104293400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr4:104293400-104294200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr4:104293400-104294400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr4:104293600-104294000	Enhancers	H9 Cell Line	embryonic stem cell
20	chr4:104293600-104296800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr4:104293800-104294400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr4:104294000-104294200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:104294000-104296600	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr4:104294000-104296800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr4:104294200-104294400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:104294200-104295000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr4:104294200-104295800	Weak transcription	HUVEC	blood vessel
28	chr4:104294400-104295200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr4:104294400-104295400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:104294400-104298600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr4:104295000-104295600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr4:104295000-104296800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:104295200-104296800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr4:104295200-104296800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr4:104295200-104296800	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr4:104295400-104295600	Enhancers	H1 Cell Line	embryonic stem cell
37	chr4:104295400-104296000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:104295600-104295800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr4:104295600-104296000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr4:104295800-104296400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr4:104295800-104297000	Enhancers	HUVEC	blood vessel
42	chr4:104296000-104296600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr4:104296000-104296600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:104296200-104297000	Enhancers	Muscle Satellite Cultured Cells	--
45	chr4:104296200-104297000	Enhancers	NH-A	brain
46	chr4:104296400-104296600	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr4:104296400-104296800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:104296400-104296800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
49	chr4:104296600-104296800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr4:104296600-104296800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell

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