Variant report

Variant	esv1833916
Chromosome Location	chr4:95673181-95679741
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:256)
CpG islands
(count:489)
Chromatin interactive
region (count:9)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:95679125-95679401	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr4:95673881-95674174	K562	blood:	n/a	chr4:95674019-95674030
3	CEBPB	chr4:95673875-95674177	H1-hESC	embryonic stem cell:	n/a	chr4:95674019-95674030
4	CEBPB	chr4:95673911-95674176	Hela-S3	cervix:	n/a	chr4:95674019-95674030
5	CEBPB	chr4:95673845-95674199	HepG2	liver:	n/a	chr4:95674019-95674030
6	CEBPB	chr4:95673863-95674189	A549	lung:	n/a	chr4:95674019-95674030
7	CEBPB	chr4:95673850-95674154	IMR90	lung:	n/a	chr4:95674019-95674030
8	CHD1	chr4:95677993-95680028	IMR90	lung:	n/a	chr4:95679126-95679136 chr4:95679131-95679141
9	CHD2	chr4:95678813-95679126	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr4:95678728-95679047	A549	lung:	n/a	n/a
11	CTBP2	chr4:95678812-95680327	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr4:95677740-95677890	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr4:95678900-95679050	AG09309	skin:	n/a	n/a
14	CTCF	chr4:95677760-95677910	HRE	kidney:	n/a	n/a
15	CTCF	chr4:95678880-95679030	MCF-7	breast:	n/a	n/a
16	CTCF	chr4:95678931-95678986	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr4:95678900-95679050	HMEC	breast:	n/a	n/a
18	CTCF	chr4:95677800-95677950	HAc	cerebellar:	n/a	n/a
19	CTCF	chr4:95678900-95679050	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr4:95677680-95677830	HRE	kidney:	n/a	n/a
21	CTCF	chr4:95677680-95677830	HMEC	breast:	n/a	n/a
22	CTCF	chr4:95677560-95677710	SAEC	small airway:	n/a	n/a
23	CTCF	chr4:95677720-95677870	BE2_C	brain:	n/a	n/a
24	CTCF	chr4:95677640-95677790	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr4:95678860-95679010	AG10803	skin:	n/a	n/a
26	CTCF	chr4:95677700-95677850	BE2_C	brain:	n/a	n/a
27	CTCF	chr4:95677760-95677910	MCF-7	breast:	n/a	n/a
28	CTCF	chr4:95677620-95677770	AG10803	skin:	n/a	n/a
29	CTCF	chr4:95678940-95679090	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr4:95678900-95679050	HAc	cerebellar:	n/a	n/a
31	CTCF	chr4:95678840-95678990	NHEK	skin:	n/a	n/a
32	CTCF	chr4:95678814-95679007	Fibrobl	skin:	n/a	n/a
33	CTCF	chr4:95677720-95677870	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr4:95677720-95677870	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr4:95678885-95678981	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:95678860-95679010	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr4:95678909-95678923	LNCaP	prostate:	n/a	n/a
38	CTCF	chr4:95677800-95677950	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr4:95678860-95679010	AG04449	skin:	n/a	n/a
40	CTCF	chr4:95678791-95679131	IMR90	lung:	n/a	n/a
41	CTCF	chr4:95678900-95679050	SAEC	small airway:	n/a	n/a
42	CTCF	chr4:95678860-95679010	A549	lung:	n/a	n/a
43	CTCF	chr4:95678867-95679012	A549	lung:	n/a	n/a
44	CTCF	chr4:95678940-95679090	HFF	foreskin:	n/a	n/a
45	CTCF	chr4:95678880-95679030	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr4:95678820-95678970	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr4:95678680-95678830	HVMF	connective:	n/a	n/a
48	CTCF	chr4:95678860-95679010	HCFaa	heart:	n/a	n/a
49	CTCF	chr4:95678900-95678912	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:95678860-95679010	WERI-Rb-1	eye:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:95678703-95678753	GM19239	blood:	n/a
2	chr4:95678703-95678753	GM19239	blood:	n/a
3	chr4:95676253-95676303	GM19239	blood:	n/a
4	chr4:95678817-95678867	LNCaP	prostate:	n/a
5	chr4:95679381-95679431	Caco-2	colon:	n/a
6	chr4:95678817-95678867	Hela-S3	cervix:	n/a
7	chr4:95678939-95678989	AG04449	skin:	fetal
8	chr4:95679705-95679755	BJ	skin:	n/a
9	chr4:95678817-95678867	HCF	heart:	n/a
10	chr4:95676253-95676303	HRCEpiC	kidney:	n/a
11	chr4:95678817-95678867	RPTEC	kidney:	n/a
12	chr4:95678703-95678753	AG09319	gingival:	n/a
13	chr4:95676253-95676303	K562	blood:	n/a
14	chr4:95678939-95678989	PANC-1	pancreas:	n/a
15	chr4:95676253-95676303	MCF10A-Er-Src	breast:	n/a
16	chr4:95679381-95679431	GM12891	blood:	n/a
17	chr4:95679705-95679755	PrEC	prostate:	n/a
18	chr4:95678939-95678989	Hepatocyte	liver:	n/a
19	chr4:95679705-95679755	Jurkat	blood:	n/a
20	chr4:95679705-95679755	HMEC	breast:	n/a
21	chr4:95678703-95678753	ECC-1	luminal epithelium:	n/a
22	chr4:95678703-95678753	A549	lung:	n/a
23	chr4:95678703-95678753	HUVEC	blood vessel:	n/a
24	chr4:95678703-95678753	HCT-116	colon:	n/a
25	chr4:95678817-95678867	HCM	heart:	n/a
26	chr4:95679705-95679755	HL-60	blood:	n/a
27	chr4:95679381-95679431	PANC-1	pancreas:	n/a
28	chr4:95678703-95678753	HRE	kidney:	n/a
29	chr4:95679381-95679431	RPTEC	kidney:	n/a
30	chr4:95678817-95678867	GM12892	blood:	n/a
31	chr4:95678703-95678753	ovcar-3	ovarian:	n/a
32	chr4:95678817-95678867	GM19239	blood:	n/a
33	chr4:95678918-95678968	ProgFib	skin:	n/a
34	chr4:95678939-95678989	GM12891	blood:	n/a
35	chr4:95679705-95679755	U87	brain:	n/a
36	chr4:95678939-95678989	GM12878	blood:	n/a
37	chr4:95678703-95678753	Hela-S3	cervix:	n/a
38	chr4:95676253-95676303	ovcar-3	ovarian:	n/a
39	chr4:95679705-95679755	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:95678703-95678753	AoSMC	blood vessel:	n/a
41	chr4:95678817-95678867	AG04449	skin:	fetal
42	chr4:95679705-95679755	Caco-2	colon:	n/a
43	chr4:95678898-95678948	NT2-D1	testis:	n/a
44	chr4:95676253-95676303	HMEC	breast:	n/a
45	chr4:95678898-95678948	HMEC	breast:	n/a
46	chr4:95678918-95678968	SK-N-MC	brain:	n/a
47	chr4:95676253-95676303	GM06990	blood:	n/a
48	chr4:95678898-95678948	H1-hESC	embryonic stem cell:	embryo
49	chr4:95678898-95678948	AG09319	gingival:	n/a
50	chr4:95678918-95678968	SAEC	small airway:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:95679187..95680719-chr4:95971290..95974263,2	MCF-7	breast:
2	chr4:95664983..95667427-chr4:95675236..95677309,2	MCF-7	breast:
3	chr4:95678678..95680883-chr4:96023985..96026151,2	MCF-7	breast:
4	chr4:95679588..95681847-chr4:96013272..96015095,2	MCF-7	breast:
5	chr4:95674754..95677008-chr4:95678687..95680473,3	MCF-7	breast:
6	chr4:95676013..95677513-chr6:26054520..26056676,2	K562	blood:
7	chr4:95674399..95676484-chr4:95676638..95680232,3	MCF-7	breast:
8	chr4:95675993..95678993-chr6:26054520..26056880,3	K562	blood:
9	chr4:95671224..95673662-chr4:95677934..95679824,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC5C-1	chr4:95678545-95679036	NONHSAT097457
2	lnc-UNC5C-1	chr4:95675981-95676056	XLOC_004019
3	lnc-UNC5C-1	chr4:95678545-95678684	XLOC_004019
4	lnc-UNC5C-1	chr4:95678545-95679011	XLOC_004019
5	lnc-UNC5C-1	chr4:95675981-95676056	NONHSAT097457
6	lnc-UNC5C-1	chr4:95675981-95676056	XLOC_004019

No data

Variant related genes	Relation type
ENSG00000249599	TF binding region
BMPR1B	TF binding region
ENSG00000249599	CpG island
BMPR1B	CpG island
ENSG00000138696	chromatin interactions
ENSG00000187837	chromatin interactions
ENSG00000249599	chromatin interactions
KIF2A	miRNA target sites

Extended variants
information (count: 209 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:209 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7681088	chr4:95673181-95673182	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562408674	chr4:95673298-95673299	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs577373898	chr4:95673316-95673317	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs539860969	chr4:95673331-95673332	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553354729	chr4:95673384-95673385	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs150556387	chr4:95673481-95673482	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs139587496	chr4:95673499-95673500	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs562356577	chr4:95673502-95673503	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs149722965	chr4:95673529-95673530	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs187199680	chr4:95673541-95673542	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs557565001	chr4:95673549-95673550	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs551021469	chr4:95673556-95673557	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs532836579	chr4:95673574-95673575	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs546193042	chr4:95673587-95673588	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs559706159	chr4:95673652-95673653	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs112368717	chr4:95673682-95673683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548984146	chr4:95673683-95673684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569068350	chr4:95673686-95673687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537656952	chr4:95673690-95673691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551572596	chr4:95673694-95673695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570959033	chr4:95673702-95673703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539899517	chr4:95673808-95673809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553446498	chr4:95673840-95673841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573153645	chr4:95673892-95673893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111417912	chr4:95673907-95673908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376728923	chr4:95673922-95673923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536177340	chr4:95673951-95673952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539562961	chr4:95673952-95673953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143984704	chr4:95674045-95674046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374177397	chr4:95674076-95674077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192781320	chr4:95674094-95674095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373203058	chr4:95674181-95674182	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs79187692	chr4:95674205-95674206	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs184869598	chr4:95674232-95674233	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs78299282	chr4:95674276-95674277	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs560120508	chr4:95674289-95674290	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs528866857	chr4:95674295-95674296	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs542574366	chr4:95674323-95674324	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs1509618	chr4:95674341-95674342	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs534874576	chr4:95674344-95674345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552840867	chr4:95674358-95674359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574441519	chr4:95674365-95674366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189284053	chr4:95674430-95674431	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs556574867	chr4:95674431-95674432	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs146438361	chr4:95674470-95674471	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs147493222	chr4:95674471-95674472	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs180828543	chr4:95674487-95674488	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs545602420	chr4:95674492-95674493	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs547097274	chr4:95674497-95674498	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs566894857	chr4:95674498-95674499	Weak transcription	Chromatin interactive region	2 gene(s)	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
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
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
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
Breast cancer	22522925	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95672200-95675000	Weak transcription	A549	lung
2	chr4:95674000-95674200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr4:95675000-95677600	Enhancers	A549	lung
4	chr4:95675600-95676000	Enhancers	Aorta	Aorta
5	chr4:95676000-95677800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:95676000-95678200	Weak transcription	Aorta	Aorta
7	chr4:95676800-95677000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:95677400-95677600	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr4:95677400-95678000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:95677400-95678000	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr4:95677600-95677800	Flanking Active TSS	A549	lung
12	chr4:95677600-95678000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:95677800-95678000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr4:95677800-95678000	Enhancers	HUVEC	blood vessel
15	chr4:95677800-95678200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr4:95677800-95681800	Active TSS	A549	lung
17	chr4:95678000-95678200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:95678000-95678200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:95678000-95678200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:95678000-95678200	Active TSS	Rectal Smooth Muscle	rectum
21	chr4:95678000-95678400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:95678000-95678400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
23	chr4:95678000-95678800	Flanking Active TSS	HUVEC	blood vessel
24	chr4:95678000-95679000	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
25	chr4:95678000-95680000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr4:95678000-95680200	Active TSS	NH-A	brain
27	chr4:95678000-95682000	Active TSS	Stomach Smooth Muscle	stomach
28	chr4:95678200-95678400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr4:95678200-95678400	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:95678200-95678400	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr4:95678200-95678400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
32	chr4:95678200-95678400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
33	chr4:95678200-95678400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr4:95678200-95678400	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr4:95678200-95678400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr4:95678200-95678400	Flanking Active TSS	NHEK	skin
37	chr4:95678200-95678600	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
38	chr4:95678200-95678600	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
39	chr4:95678200-95678600	Bivalent/Poised TSS	Fetal Kidney	kidney
40	chr4:95678200-95678600	Bivalent Enhancer	NHDF-Ad	bronchial
41	chr4:95678200-95678800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr4:95678200-95678800	Bivalent Enhancer	Fetal Brain Male	brain
43	chr4:95678200-95679000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
44	chr4:95678200-95679000	Flanking Bivalent TSS/Enh	Dnd41	blood
45	chr4:95678200-95679600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
46	chr4:95678200-95680000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:95678200-95680400	Active TSS	Aorta	Aorta
48	chr4:95678200-95680400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
49	chr4:95678200-95680400	Active TSS	HMEC	breast
50	chr4:95678400-95678600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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