Variant report

Variant	nsv909475
Chromosome Location	chr18:24687324-24776226
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	ARID3A	chr18:24722857-24723286	HepG2	liver:	n/a	n/a
2	ATF1	chr18:24692205-24692289	K562	blood:	n/a	n/a
3	ATF1	chr18:24707007-24707009	K562	blood:	n/a	n/a
4	ATF1	chr18:24761884-24761917	K562	blood:	n/a	n/a
5	ATF1	chr18:24761429-24761582	K562	blood:	n/a	n/a
6	ATF1	chr18:24763423-24763503	K562	blood:	n/a	n/a
7	ATF3	chr18:24716186-24716326	HepG2	liver:	n/a	n/a
8	BACH1	chr18:24709050-24709054	K562	blood:	n/a	n/a
9	BACH1	chr18:24702204-24702331	K562	blood:	n/a	n/a
10	BACH1	chr18:24764352-24764632	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr18:24765163-24765182	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr18:24716111-24716471	HepG2	liver:	n/a	n/a
13	BHLHE40	chr18:24715587-24715933	GM12878	blood:	n/a	n/a
14	CBX3	chr18:24729202-24729532	K562	blood:	n/a	n/a
15	CEBPB	chr18:24774998-24775161	K562	blood:	n/a	chr18:24775040-24775051
16	CEBPB	chr18:24716115-24716315	K562	blood:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
17	CEBPB	chr18:24775015-24775170	A549	lung:	n/a	chr18:24775040-24775051
18	CEBPB	chr18:24716143-24716486	HepG2	liver:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
19	CEBPB	chr18:24716155-24716411	MCF-7	breast:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
20	CEBPB	chr18:24716019-24716509	ECC-1	luminal epithelium:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
21	CEBPB	chr18:24716052-24716403	A549	lung:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
22	CEBPB	chr18:24716125-24716411	IMR90	lung:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
23	CEBPB	chr18:24716064-24716457	HepG2	liver:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
24	CEBPB	chr18:24716065-24716475	H1-hESC	embryonic stem cell:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
25	CEBPB	chr18:24705001-24705243	HepG2	liver:	n/a	chr18:24705124-24705135
26	CEBPB	chr18:24716078-24716533	HepG2	liver:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
27	CEBPB	chr18:24716006-24716558	ECC-1	luminal epithelium:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
28	CEBPB	chr18:24715992-24716485	A549	lung:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
29	CEBPB	chr18:24767247-24767461	HepG2	liver:	n/a	chr18:24767358-24767369 chr18:24767399-24767412
30	CEBPB	chr18:24716122-24716427	A549	lung:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
31	CEBPB	chr18:24774994-24775125	H1-hESC	embryonic stem cell:	n/a	chr18:24775040-24775051
32	CEBPB	chr18:24716131-24716369	HepG2	liver:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
33	CEBPB	chr18:24774989-24775189	HepG2	liver:	n/a	chr18:24775040-24775051
34	CEBPB	chr18:24716075-24716429	Hela-S3	cervix:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
35	CEBPD	chr18:24716085-24716354	HepG2	liver:	n/a	n/a
36	CTBP2	chr18:24764215-24765120	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr18:24743285-24743409	GM13977	blood:	n/a	n/a
38	CTCF	chr18:24743311-24743459	NHEK	skin:	n/a	n/a
39	CTCF	chr18:24743220-24743370	GM12874	blood:	n/a	n/a
40	CTCF	chr18:24692419-24692462	LNCaP	prostate:	n/a	n/a
41	CTCF	chr18:24765487-24765551	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr18:24743340-24743490	GM12878	blood:	n/a	n/a
43	CTCF	chr18:24743265-24743493	LNCaP	prostate:	n/a	n/a
44	CTCF	chr18:24743240-24743390	NHEK	skin:	n/a	n/a
45	CTCF	chr18:24743220-24743370	BE2_C	brain:	n/a	n/a
46	CTCF	chr18:24743240-24743390	GM12871	blood:	n/a	n/a
47	CTCF	chr18:24771430-24771449	K562	blood:	n/a	n/a
48	CTCF	chr18:24703120-24703270	GM12869	blood:	n/a	n/a
49	CTCF	chr18:24743220-24743370	NHEK	skin:	n/a	n/a
50	CTCF	chr18:24764600-24764750	Caco-2	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:24765485-24765535	HRE	kidney:	n/a
2	chr18:24764966-24765016	NB4	blood:	n/a
3	chr18:24765643-24765693	MCF-7	breast:	n/a
4	chr18:24762316-24762366	HCT-116	colon:	n/a
5	chr18:24764599-24764649	GM06990	blood:	n/a
6	chr18:24765119-24765169	Caco-2	colon:	n/a
7	chr18:24762316-24762366	PANC-1	pancreas:	n/a
8	chr18:24765119-24765169	HCM	heart:	n/a
9	chr18:24765490-24765540	NHDF-neo	bronchial:	n/a
10	chr18:24765490-24765540	LNCaP	prostate:	n/a
11	chr18:24765490-24765540	HRPEpiC	eye:	n/a
12	chr18:24764966-24765016	SK-N-SH	brain:	n/a
13	chr18:24765781-24765831	NHBE	bronchial:	n/a
14	chr18:24765490-24765540	SK-N-SH_RA	brain:	n/a
15	chr18:24764599-24764649	AG09319	gingival:	n/a
16	chr18:24765485-24765535	SK-N-SH	brain:	n/a
17	chr18:24765154-24765204	PrEC	prostate:	n/a
18	chr18:24765473-24765523	Jurkat	blood:	n/a
19	chr18:24764599-24764649	PFSK-1	brain:	n/a
20	chr18:24765643-24765693	Hela-S3	cervix:	n/a
21	chr18:24764966-24765016	HMEC	breast:	n/a
22	chr18:24765119-24765169	ProgFib	skin:	n/a
23	chr18:24762316-24762366	GM06990	blood:	n/a
24	chr18:24764599-24764649	AG09309	skin:	n/a
25	chr18:24765485-24765535	MCF-7	breast:	n/a
26	chr18:24765485-24765535	GM12891	blood:	n/a
27	chr18:24765490-24765540	ProgFib	skin:	n/a
28	chr18:24765154-24765204	HRPEpiC	eye:	n/a
29	chr18:24765154-24765204	Hepatocyte	liver:	n/a
30	chr18:24765643-24765693	RPTEC	kidney:	n/a
31	chr18:24765485-24765535	Hepatocyte	liver:	n/a
32	chr18:24764599-24764649	K562	blood:	n/a
33	chr18:24762316-24762366	AoSMC	blood vessel:	n/a
34	chr18:24765490-24765540	HEK293	kidney:	embryo
35	chr18:24765154-24765204	MCF-7	breast:	n/a
36	chr18:24765154-24765204	HCF	heart:	n/a
37	chr18:24765119-24765169	AG04449	skin:	fetal
38	chr18:24765154-24765204	SKMC	muscle:	n/a
39	chr18:24765490-24765540	SK-N-SH	brain:	n/a
40	chr18:24765781-24765831	SK-N-SH_RA	brain:	n/a
41	chr18:24765490-24765540	ECC-1	luminal epithelium:	n/a
42	chr18:24765473-24765523	HIPEpiC	eye:	n/a
43	chr18:24765643-24765693	HMEC	breast:	n/a
44	chr18:24764599-24764649	MCF-7	breast:	n/a
45	chr18:24765485-24765535	HUVEC	blood vessel:	n/a
46	chr18:24765781-24765831	HRCEpiC	kidney:	n/a
47	chr18:24765643-24765693	NHDF-neo	bronchial:	n/a
48	chr18:24765485-24765535	HMEC	breast:	n/a
49	chr18:24765473-24765523	PANC-1	pancreas:	n/a
50	chr18:24765781-24765831	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:24587162..24589841-chr18:24735427..24737669,2	K562	blood:
2	chr18:24734168..24736128-chr18:24762446..24765149,2	K562	blood:
3	chr18:24734168..24736128-chr18:24762446..24765149,2	K562	blood:
4	chr18:24744878..24747343-chr18:24750374..24752456,2	K562	blood:
5	chr18:24712355..24714811-chr18:24718073..24719662,2	MCF-7	breast:
6	chr18:24754408..24756988-chr18:24763307..24765193,2	K562	blood:
7	chr18:24770863..24773354-chr18:24775315..24777406,2	K562	blood:
8	chr18:24754408..24756988-chr18:24763307..24765193,2	K562	blood:
9	chr18:24744878..24747343-chr18:24750374..24752456,2	K562	blood:
10	chr18:24770863..24773354-chr18:24775315..24777406,2	K562	blood:
11	chr18:24712355..24714811-chr18:24718073..24719662,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAF4B-4	chr18:24768707-24770662	ENSG00000260372.2
2	lnc-TAF4B-4	chr18:24727662-24727742	ENSG00000260372.2

Variant related genes	Relation type
CHST9	TF binding region
CHST9	CpG island

Extended variants
information (count: 3110 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3110 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9961915	chr18:24687324-24687325	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
2	rs7240658	chr18:24687347-24687348	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs9953270	chr18:24687371-24687372	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
4	rs540034903	chr18:24687386-24687387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565064787	chr18:24687387-24687388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147552023	chr18:24687416-24687417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555911605	chr18:24687520-24687521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550808905	chr18:24687549-24687550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569159055	chr18:24687555-24687556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116283057	chr18:24687592-24687593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548313776	chr18:24687606-24687607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566610169	chr18:24687607-24687608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187928965	chr18:24687678-24687679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565527695	chr18:24687709-24687710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558907008	chr18:24687711-24687712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs72884327	chr18:24687733-24687734	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs113961273	chr18:24687745-24687746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538161535	chr18:24687748-24687749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556813536	chr18:24687757-24687758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575351380	chr18:24687777-24687778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536240483	chr18:24687797-24687798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72884328	chr18:24687843-24687844	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs572005575	chr18:24687847-24687848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377414144	chr18:24687860-24687861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540291413	chr18:24687881-24687882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569430192	chr18:24687884-24687885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76268292	chr18:24687910-24687911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544223756	chr18:24687911-24687912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562431345	chr18:24687913-24687914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530069087	chr18:24687916-24687917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548156766	chr18:24687930-24687931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555122559	chr18:24687943-24687944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144916656	chr18:24688052-24688053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567171206	chr18:24688063-24688064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs145831499	chr18:24688085-24688086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116767254	chr18:24688106-24688107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191207816	chr18:24688174-24688175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148975334	chr18:24688251-24688252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374031445	chr18:24688272-24688273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560250971	chr18:24688299-24688300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs61486190	chr18:24688303-24688304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550243027	chr18:24688314-24688315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568751930	chr18:24688326-24688327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs184602490	chr18:24688338-24688339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377742256	chr18:24688398-24688399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189467004	chr18:24688418-24688419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181457590	chr18:24688445-24688446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572838199	chr18:24688463-24688464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533651092	chr18:24688464-24688465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558614710	chr18:24688466-24688467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Glioblastoma multiforme	21922591	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	19651600	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:605 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24679000-24691400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr18:24679600-24688000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr18:24685000-24689000	Weak transcription	Fetal Brain Male	brain
4	chr18:24688000-24689400	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr18:24689000-24689200	Enhancers	H9 Cell Line	embryonic stem cell
6	chr18:24689000-24690000	Enhancers	Fetal Brain Male	brain
7	chr18:24689000-24691200	Enhancers	Fetal Stomach	stomach
8	chr18:24689200-24693200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr18:24689200-24703600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr18:24689400-24691400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr18:24689600-24690000	Enhancers	Fetal Brain Female	brain
12	chr18:24690000-24691800	Weak transcription	Fetal Brain Male	brain
13	chr18:24690400-24690600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr18:24690600-24691600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr18:24691400-24691600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr18:24691400-24692000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr18:24691400-24692000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
18	chr18:24691600-24691800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr18:24691800-24693200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr18:24692000-24693200	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr18:24692000-24693400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr18:24693200-24694800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr18:24693200-24695200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
24	chr18:24693400-24693600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr18:24693400-24694200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
26	chr18:24693600-24707200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr18:24694200-24699400	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr18:24695200-24699200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr18:24697600-24697800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr18:24697800-24699000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr18:24698600-24698800	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr18:24698600-24698800	ZNF genes & repeats	Pancreas	Pancrea
33	chr18:24698800-24700200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr18:24698800-24715600	Weak transcription	Pancreas	Pancrea
35	chr18:24699000-24699200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr18:24699200-24699600	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr18:24699200-24699800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr18:24699200-24700000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr18:24699400-24700200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr18:24699600-24700000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr18:24699600-24701800	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr18:24699800-24700800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr18:24700000-24701200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr18:24700000-24701600	Enhancers	Muscle Satellite Cultured Cells	--
45	chr18:24700000-24703400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr18:24700000-24703800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr18:24700200-24701200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr18:24700200-24703000	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr18:24701200-24701400	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr18:24701400-24701600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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