Variant report

Variant	nsv909292
Chromosome Location	chr18:533191-618124
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:899)
CpG islands
(count:1464)
Chromatin interactive
region (count:67)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:899 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:572540-572852	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:616346-616735	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:597008-597221	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:616381-616786	K562	blood:	n/a	n/a
5	ARID3A	chr18:618000-618431	K562	blood:	n/a	n/a
6	ARID3A	chr18:577622-577755	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:604881-605042	K562	blood:	n/a	n/a
8	ATF1	chr18:596993-597072	K562	blood:	n/a	n/a
9	ATF1	chr18:617989-618290	K562	blood:	n/a	n/a
10	ATF1	chr18:616584-616586	K562	blood:	n/a	n/a
11	ATF2	chr18:596947-597269	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr18:617970-618407	K562	blood:	n/a	n/a
13	BACH1	chr18:574849-575169	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr18:597008-597243	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL3	chr18:617913-618566	K562	blood:	n/a	n/a
16	BCL3	chr18:557398-557643	GM12878	blood:	n/a	n/a
17	BHLHE40	chr18:597007-597159	GM12878	blood:	n/a	n/a
18	BHLHE40	chr18:604841-605140	K562	blood:	n/a	n/a
19	BHLHE40	chr18:616485-616636	GM12878	blood:	n/a	n/a
20	BHLHE40	chr18:616519-616588	K562	blood:	n/a	n/a
21	BHLHE40	chr18:596915-597242	K562	blood:	n/a	n/a
22	BHLHE40	chr18:596967-597251	HepG2	liver:	n/a	n/a
23	BHLHE40	chr18:617993-618371	K562	blood:	n/a	n/a
24	BHLHE40	chr18:570718-570900	HepG2	liver:	n/a	n/a
25	BRCA1	chr18:597067-597178	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr18:616425-616625	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr18:596938-597263	K562	blood:	n/a	n/a
28	CBX3	chr18:580040-580662	K562	blood:	n/a	n/a
29	CBX3	chr18:617910-618403	K562	blood:	n/a	n/a
30	CBX3	chr18:617845-618456	K562	blood:	n/a	n/a
31	CCNT2	chr18:617908-618445	K562	blood:	n/a	n/a
32	CCNT2	chr18:580269-580459	K562	blood:	n/a	n/a
33	CCNT2	chr18:596910-597210	K562	blood:	n/a	n/a
34	CEBPB	chr18:617855-618492	K562	blood:	n/a	n/a
35	CEBPB	chr18:564762-564984	HepG2	liver:	n/a	chr18:564871-564882
36	CEBPB	chr18:615095-615305	HepG2	liver:	n/a	chr18:615198-615209 chr18:615196-615207
37	CEBPB	chr18:597013-597205	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr18:581236-581482	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr18:574971-575160	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr18:615115-615289	A549	lung:	n/a	chr18:615198-615209 chr18:615196-615207
41	CEBPB	chr18:615047-615310	K562	blood:	n/a	chr18:615198-615209 chr18:615196-615207
42	CEBPB	chr18:568517-569214	MCF-7	breast:	n/a	n/a
43	CEBPB	chr18:564759-564923	HepG2	liver:	n/a	chr18:564871-564882
44	CEBPB	chr18:568678-569237	MCF-7	breast:	n/a	n/a
45	CEBPB	chr18:577670-577824	HepG2	liver:	n/a	n/a
46	CEBPB	chr18:614980-615361	K562	blood:	n/a	chr18:615198-615209 chr18:615196-615207
47	CEBPB	chr18:577631-577852	HepG2	liver:	n/a	n/a
48	CEBPB	chr18:558596-558604	K562	blood:	n/a	n/a
49	CEBPD	chr18:617840-618573	K562	blood:	n/a	n/a
50	CEBPD	chr18:617904-618483	K562	blood:	n/a	n/a

(count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:580258-580308	SK-N-SH_RA	brain:	n/a
2	chr18:581171-581221	AoSMC	blood vessel:	n/a
3	chr18:579713-579763	GM12892	blood:	n/a
4	chr18:580258-580308	GM12891	blood:	n/a
5	chr18:596757-596807	PFSK-1	brain:	n/a
6	chr18:580188-580238	HCM	heart:	n/a
7	chr18:581171-581221	BE2_C	brain:	n/a
8	chr18:615936-615986	NHBE	bronchial:	n/a
9	chr18:597075-597125	SK-N-SH_RA	brain:	n/a
10	chr18:616707-616757	HRCEpiC	kidney:	n/a
11	chr18:615471-615521	T-47D	breast:	n/a
12	chr18:579713-579763	MCF10A-Er-Src	breast:	n/a
13	chr18:580258-580308	PANC-1	pancreas:	n/a
14	chr18:596759-596809	BE2_C	brain:	n/a
15	chr18:580209-580259	ECC-1	luminal epithelium:	n/a
16	chr18:579713-579763	NHBE	bronchial:	n/a
17	chr18:581171-581221	HCPEpiC	choroid plexus:	n/a
18	chr18:597075-597125	A549	lung:	n/a
19	chr18:580228-580278	H1-hESC	embryonic stem cell:	embryo
20	chr18:596713-596763	NHBE	bronchial:	n/a
21	chr18:596757-596807	HCPEpiC	choroid plexus:	n/a
22	chr18:615936-615986	SK-N-SH	brain:	n/a
23	chr18:616707-616757	IMR90	lung:	fetal
24	chr18:615936-615986	H1-hESC	embryonic stem cell:	embryo
25	chr18:580228-580278	Hela-S3	cervix:	n/a
26	chr18:615936-615986	NHDF-neo	bronchial:	n/a
27	chr18:580209-580259	HEK293	kidney:	embryo
28	chr18:597111-597161	GM12878	blood:	n/a
29	chr18:596759-596809	A549	lung:	n/a
30	chr18:597111-597161	Hepatocyte	liver:	n/a
31	chr18:580334-580384	HRPEpiC	eye:	n/a
32	chr18:596759-596809	Caco-2	colon:	n/a
33	chr18:596943-596993	A549	lung:	n/a
34	chr18:581171-581221	RPTEC	kidney:	n/a
35	chr18:615496-615546	ovcar-3	ovarian:	n/a
36	chr18:615471-615521	HL-60	blood:	n/a
37	chr18:580334-580384	GM06990	blood:	n/a
38	chr18:597111-597161	SAEC	small airway:	n/a
39	chr18:596757-596807	HCM	heart:	n/a
40	chr18:580209-580259	HRPEpiC	eye:	n/a
41	chr18:580258-580308	NH-A	brain:	n/a
42	chr18:616707-616757	AG04449	skin:	fetal
43	chr18:615471-615521	LNCaP	prostate:	n/a
44	chr18:616707-616757	NHDF-neo	bronchial:	n/a
45	chr18:615936-615986	HRE	kidney:	n/a
46	chr18:579713-579763	BJ	skin:	n/a
47	chr18:580435-580485	HRCEpiC	kidney:	n/a
48	chr18:579237-579287	HRCEpiC	kidney:	n/a
49	chr18:581171-581221	HCT-116	colon:	n/a
50	chr18:615496-615546	BJ	skin:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:588087..590665-chr18:658985..661981,2	K562	blood:
2	chr18:527640..529801-chr18:531876..533753,2	K562	blood:
3	chr18:569366..571710-chr18:576690..578191,2	K562	blood:
4	chr18:581007..582847-chr18:587987..590964,2	MCF-7	breast:
5	chr18:583208..586140-chr18:590268..592916,3	MCF-7	breast:
6	chr18:614379..615931-chr18:3664967..3667055,2	K562	blood:
7	chr18:513812..515978-chr18:595645..597205,2	MCF-7	breast:
8	chr18:610818..612992-chr18:660129..662182,2	K562	blood:
9	chr18:596612..597183-chr18:616160..617004,2	MCF-7	breast:
10	chr18:597037..597571-chr18:612004..612507,2	K562	blood:
11	chr18:596793..597621-chr18:616099..617012,5	K562	blood:
12	chr18:596672..598254-chr18:601606..603609,2	MCF-7	breast:
13	chr18:533036..535314-chr18:564688..567165,2	K562	blood:
14	chr18:599119..600795-chr18:610361..612404,2	K562	blood:
15	chr18:616365..618301-chr18:3603481..3605201,2	K562	blood:
16	chr12:6960313..6962763-chr18:595597..598209,2	MCF-7	breast:
17	chr18:581007..582847-chr18:587987..590964,2	MCF-7	breast:
18	chr18:616552..618789-chr18:3651360..3654068,2	K562	blood:
19	chr18:603691..606447-chr18:810738..812347,2	K562	blood:
20	chr18:602377..604828-chr18:613978..616392,2	K562	blood:
21	chr18:569366..571710-chr18:576690..578191,2	K562	blood:
22	chr18:499109..499807-chr18:568417..568974,2	MCF-7	breast:
23	chr18:615731..618024-chr18:3602454..3604575,2	K562	blood:
24	chr18:602193..605020-chr18:611416..613550,2	K562	blood:
25	chr18:596612..597183-chr18:616160..617004,2	MCF-7	breast:
26	chr18:544917..547338-chr18:550770..553132,2	MCF-7	breast:
27	chr18:544938..547382-chr18:549266..550898,2	MCF-7	breast:
28	chr18:596672..598254-chr18:601606..603609,2	MCF-7	breast:
29	chr18:577506..581309-chr18:585130..588053,4	K562	blood:
30	chr18:598315..601493-chr18:602058..605759,5	K562	blood:
31	chr18:291631..293957-chr18:611359..613782,2	MCF-7	breast:
32	chr18:292167..293133-chr18:616102..616665,2	MCF-7	breast:
33	chr18:577506..581309-chr18:585130..588053,4	K562	blood:
34	chr18:583208..586140-chr18:590268..592916,3	MCF-7	breast:
35	chr18:531981..533671-chr18:545540..547147,2	K562	blood:
36	chr18:606223..607913-chr18:611491..614065,2	K562	blood:
37	chr18:597037..597571-chr18:612004..612507,2	K562	blood:
38	chr18:600276..602735-chr18:648496..651246,2	K562	blood:
39	chr18:266158..268962-chr18:568769..571173,2	MCF-7	breast:
40	chr18:551807..553605-chr18:554832..557519,2	K562	blood:
41	chr18:551807..553605-chr18:554832..557519,2	K562	blood:
42	chr18:570210..572740-chr18:576690..579289,2	K562	blood:
43	chr18:599119..600795-chr18:610361..612404,2	K562	blood:
44	chr18:596793..597621-chr18:616099..617012,5	K562	blood:
45	chr18:531981..533671-chr18:545540..547147,2	K562	blood:
46	chr18:606223..607913-chr18:611491..614065,2	K562	blood:
47	chr18:570210..572740-chr18:576690..579289,2	K562	blood:
48	chr18:266563..269513-chr18:596555..599263,2	K562	blood:
49	chr18:610723..612346-chr18:616387..618431,2	K562	blood:
50	chr18:532145..533671-chr18:545647..547394,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CETN1-2	chr18:560665-560921	l_1508_chr18:548299-561069_testes
2	lnc-CLUL1-2	chr18:606978-607099	NONHSAT056848
3	lnc-C18orf56-2	chr18:586517-586850	NONHSAT056846
4	lnc-CETN1-2	chr18:548300-548363	l_1508_chr18:548299-561069_testes
5	lnc-CLUL1-2	chr18:614508-614797	NONHSAT056848
6	lnc-CLUL1-2	chr18:612765-612911	NONHSAT056847
7	lnc-CETN1-1	chr18:570665-571069	XLOC_012602
8	lnc-CETN1-1	chr18:558300-558363	XLOC_012602
9	lnc-CLUL1-2	chr18:617988-618087	NONHSAT056847
10	lnc-CLUL1-2	chr18:606978-607099	NONHSAT056847
11	lnc-CLUL1-2	chr18:596998-597129	NONHSAT056847
12	lnc-CETN1-2	chr18:560929-561069	l_1508_chr18:548299-561069_testes
13	lnc-CLUL1-2	chr18:597002-597129	NONHSAT056848

No data

Variant related genes	Relation type
RN7SKP146	TF binding region
CETN1	TF binding region
ENSG00000239158	TF binding region
CLUL1	TF binding region
RN7SKP146	CpG island
CETN1	CpG island
ENSG00000239158	CpG island
CLUL1	CpG island
ENSG00000239158	chromatin interactions
ENSG00000176912	chromatin interactions
ENSG00000079101	chromatin interactions
ENSG00000266401	chromatin interactions
ENSG00000222174	chromatin interactions
ENSG00000262001	chromatin interactions
ENSG00000176890	chromatin interactions
ENSG00000263884	chromatin interactions
ENSG00000176105	chromatin interactions
ENSG00000266456	chromatin interactions
ENSG00000263727	chromatin interactions
ENSG00000079134	chromatin interactions
ENSG00000111665	chromatin interactions
ENSG00000264265	chromatin interactions
ENSG00000177143	chromatin interactions
ENSG00000111667	chromatin interactions
ENSG00000158270	chromatin interactions

Extended variants
information (count: 3367 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3367 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1893292	chr18:533191-533192	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs12606729	chr18:533216-533217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528502777	chr18:533231-533232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546607077	chr18:533252-533253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148585914	chr18:533257-533258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34740340	chr18:533316-533317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532473863	chr18:533320-533321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576735	chr18:533368-533369	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs145710033	chr18:533395-533396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1893293	chr18:533397-533398	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs536133223	chr18:533438-533439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7245054	chr18:533463-533464	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs147716915	chr18:533476-533477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369924473	chr18:533509-533510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142573239	chr18:533547-533548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111526498	chr18:533555-533556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554519506	chr18:533561-533562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532458887	chr18:533618-533619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373812955	chr18:533635-533636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574625678	chr18:533647-533648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146505156	chr18:533660-533661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs151279823	chr18:533684-533685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543501584	chr18:533700-533701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557267733	chr18:533711-533712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189823812	chr18:533712-533713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542938991	chr18:533822-533823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369779713	chr18:533826-533827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374530600	chr18:533892-533893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573224944	chr18:533905-533906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368780432	chr18:533911-533912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181087425	chr18:533930-533931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs80002607	chr18:533931-533932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73360564	chr18:533932-533933	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs184502121	chr18:533988-533989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189027086	chr18:533992-533993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570711062	chr18:534001-534002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528736649	chr18:534029-534030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73360566	chr18:534047-534048	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs376367002	chr18:534068-534069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182483869	chr18:534083-534084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs150403584	chr18:534111-534112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs494115	chr18:534144-534145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138180016	chr18:534212-534213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552189278	chr18:534228-534229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570506074	chr18:534260-534261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs495964	chr18:534341-534342	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs186378981	chr18:534379-534380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574465632	chr18:534388-534389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs367923893	chr18:534399-534400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141603504	chr18:535615-535616	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal cancer	21851588	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Breast cancer	17899364	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Gastrointestinal cancer	17018589	CNVD
prenatal diagnosis	20453657	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Renal cell carcinoma	18765545	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Bladder cancer	21909424	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:494 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:525000-533800	Weak transcription	Gastric	stomach
2	chr18:525400-533800	Weak transcription	Pancreas	Pancrea
3	chr18:527800-534000	Weak transcription	Stomach Mucosa	stomach
4	chr18:533800-534200	Enhancers	Gastric	stomach
5	chr18:533800-534200	Enhancers	Pancreas	Pancrea
6	chr18:534000-534400	Enhancers	Stomach Mucosa	stomach
7	chr18:535600-536200	Active TSS	H9 Cell Line	embryonic stem cell
8	chr18:542600-543200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr18:542600-543200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr18:542800-544200	Enhancers	Fetal Stomach	stomach
11	chr18:542800-544800	Enhancers	Fetal Lung	lung
12	chr18:543000-543400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr18:543200-549600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr18:543600-544000	Enhancers	Duodenum Smooth Muscle	Duodenum
15	chr18:543600-544000	Enhancers	Fetal Muscle Leg	muscle
16	chr18:545200-545600	Enhancers	Spleen	Spleen
17	chr18:546200-555400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr18:546600-547200	Enhancers	HepG2	liver
19	chr18:550000-550200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr18:555400-555600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr18:555400-556400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr18:555400-557000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr18:555600-556400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr18:555600-556400	Enhancers	Fetal Stomach	stomach
25	chr18:556000-556800	Enhancers	Fetal Lung	lung
26	chr18:556400-557000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr18:556400-565200	Weak transcription	Fetal Stomach	stomach
28	chr18:556800-557000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr18:557000-557400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr18:557000-563200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr18:557400-558600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr18:558600-561400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr18:561800-562000	Weak transcription	Right Atrium	heart
34	chr18:562000-562200	ZNF genes & repeats	Right Atrium	heart
35	chr18:562000-565200	Weak transcription	Left Ventricle	heart
36	chr18:562200-564800	Weak transcription	Right Atrium	heart
37	chr18:563200-563400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr18:563400-565200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr18:564000-565800	Enhancers	Fetal Heart	heart
40	chr18:564600-565600	Enhancers	HepG2	liver
41	chr18:564600-565800	Enhancers	Fetal Lung	lung
42	chr18:564800-565000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr18:564800-565600	Enhancers	Placenta	Placenta
44	chr18:564800-565800	Enhancers	Right Atrium	heart
45	chr18:565200-565600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
46	chr18:565200-565600	Enhancers	Fetal Muscle Leg	muscle
47	chr18:565200-565600	Enhancers	Left Ventricle	heart
48	chr18:565200-565800	Enhancers	Fetal Muscle Trunk	muscle
49	chr18:565200-566000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr18:565200-566600	Enhancers	Fetal Stomach	stomach

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