Variant report

Variant	nsv909524
Chromosome Location	chr18:30115418-30196804
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	chr18:30131174-30131190	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:30129239-30129485	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:30142422-30142500	HepG2	liver:	n/a	n/a
4	BACH1	chr18:30119864-30119870	K562	blood:	n/a	n/a
5	BACH1	chr18:30190420-30190421	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr18:30178218-30178457	GM12878	blood:	n/a	n/a
7	BCL11A	chr18:30128823-30129054	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr18:30128823-30129068	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr18:30132459-30132771	GM12878	blood:	n/a	n/a
10	BHLHE40	chr18:30129259-30129459	GM12878	blood:	n/a	n/a
11	CEBPB	chr18:30193391-30193636	IMR90	lung:	n/a	chr18:30193474-30193485
12	CEBPB	chr18:30122416-30122693	MCF-7	breast:	n/a	chr18:30122580-30122593 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122580-30122591 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122582-30122593
13	CEBPB	chr18:30146615-30146815	A549	lung:	n/a	n/a
14	CEBPB	chr18:30122410-30122771	IMR90	lung:	n/a	chr18:30122580-30122593 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122580-30122591 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122582-30122593
15	CEBPB	chr18:30122425-30122688	K562	blood:	n/a	chr18:30122580-30122593 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122580-30122591 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122582-30122593
16	CEBPB	chr18:30117505-30117594	A549	lung:	n/a	n/a
17	CEBPB	chr18:30122500-30122629	HepG2	liver:	n/a	chr18:30122580-30122593 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122580-30122591 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122582-30122593
18	CEBPB	chr18:30141181-30141299	HepG2	liver:	n/a	chr18:30141235-30141246
19	CEBPB	chr18:30157849-30158073	HepG2	liver:	n/a	chr18:30157971-30157982
20	CEBPB	chr18:30157855-30158133	IMR90	lung:	n/a	chr18:30157971-30157982
21	CEBPB	chr18:30122401-30122773	HepG2	liver:	n/a	chr18:30122580-30122593 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122580-30122591 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122582-30122593
22	CEBPB	chr18:30122435-30122683	ECC-1	luminal epithelium:	n/a	chr18:30122580-30122593 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122580-30122591 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122582-30122593
23	CEBPB	chr18:30122403-30122751	Hela-S3	cervix:	n/a	chr18:30122580-30122593 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122580-30122591 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122582-30122593
24	CEBPB	chr18:30193371-30193687	HepG2	liver:	n/a	chr18:30193474-30193485
25	CEBPB	chr18:30159138-30159403	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr18:30193453-30193677	A549	lung:	n/a	chr18:30193474-30193485
27	CEBPB	chr18:30122403-30122736	H1-hESC	embryonic stem cell:	n/a	chr18:30122580-30122593 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122580-30122591 chr18:30122582-30122591 chr18:30122582-30122591 chr18:30122582-30122593
28	CHD2	chr18:30136205-30136420	K562	blood:	n/a	n/a
29	CHD2	chr18:30132430-30132793	HepG2	liver:	n/a	n/a
30	CHD2	chr18:30130908-30131239	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr18:30129311-30129495	A549	lung:	n/a	chr18:30129418-30129431
32	CREB1	chr18:30129211-30129650	H1-hESC	embryonic stem cell:	n/a	chr18:30129418-30129431
33	CREB1	chr18:30129332-30129474	A549	lung:	n/a	chr18:30129418-30129431
34	CREB1	chr18:30129310-30129517	H1-hESC	embryonic stem cell:	n/a	chr18:30129418-30129431
35	CTCF	chr18:30131013-30131160	MCF-7	breast:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
36	CTCF	chr18:30131072-30131145	HUVEC	blood vessel:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
37	CTCF	chr18:30129620-30129770	SAEC	small airway:	n/a	n/a
38	CTCF	chr18:30131020-30131170	HBMEC	blood vessel:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
39	CTCF	chr18:30129280-30129544	HepG2	liver:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
40	CTCF	chr18:30129291-30129503	ProgFib	skin:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
41	CTCF	chr18:30132520-30132670	BE2_C	brain:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
42	CTCF	chr18:30129251-30129561	MCF-7	breast:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
43	CTCF	chr18:30156340-30156490	HPF	lung:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
44	CTCF	chr18:30129340-30129490	HUVEC	blood vessel:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
45	CTCF	chr18:30129320-30129470	GM06990	blood:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
46	CTCF	chr18:30132509-30132699	GM13976	blood:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
47	CTCF	chr18:30156320-30156470	MCF-7	breast:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
48	CTCF	chr18:30129360-30129510	NHDF-neo	bronchial:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
49	CTCF	chr18:30132520-30132670	Caco-2	colon:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
50	CTCF	chr18:30129340-30129490	GM12865	blood:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414

No.	Distal block	Cell Line	Cell type
1	chr18:30156031..30156847-chr18:30254282..30255103,2	MCF-7	breast:
2	chr18:29851552..29852413-chr18:30132133..30133147,4	MCF-7	breast:
3	chr18:30133804..30136376-chr18:30138480..30140813,2	MCF-7	breast:
4	chr18:29737738..29738425-chr18:30129431..30129978,2	MCF-7	breast:
5	chr18:30124765..30126879-chr18:30130825..30132479,2	MCF-7	breast:
6	chr18:29746021..29748182-chr18:30119700..30121439,2	K562	blood:
7	chr18:30155970..30156491-chr18:30499440..30500054,2	MCF-7	breast:
8	chr18:29737720..29738653-chr18:30132086..30132779,5	K562	blood:
9	chr18:30125345..30127193-chr18:30127513..30129588,2	MCF-7	breast:
10	chr18:30049677..30051378-chr18:30146420..30148421,2	MCF-7	breast:
11	chr18:30190203..30191854-chr18:30213352..30215090,2	MCF-7	breast:
12	chr18:30133804..30136376-chr18:30138480..30140813,2	MCF-7	breast:
13	chr18:29851628..29852386-chr18:30132192..30133063,2	MCF-7	breast:
14	chr18:29913485..29914461-chr18:30129286..30129947,2	MCF-7	breast:
15	chr18:30156679..30157193-chr18:30249087..30249714,2	MCF-7	breast:
16	chr18:30132180..30132981-chr18:30253686..30254646,2	MCF-7	breast:
17	chr18:30125345..30127193-chr18:30127513..30129588,2	MCF-7	breast:
18	chr18:29869178..29870066-chr18:30128854..30129812,2	MCF-7	breast:
19	chr18:29737699..29739046-chr18:30132133..30133008,6	MCF-7	breast:
20	chr18:29851159..29852631-chr18:30128814..30129900,6	MCF-7	breast:
21	chr18:30195814..30198126-chr18:30198188..30200453,2	MCF-7	breast:
22	chr18:30155938..30156890-chr18:30249254..30250445,9	MCF-7	breast:
23	chr18:30049618..30051856-chr18:30120805..30123619,2	MCF-7	breast:
24	chr18:30049439..30053878-chr18:30126244..30131084,5	MCF-7	breast:
25	chr18:29737731..29738647-chr18:30131030..30131759,2	MCF-7	breast:
26	chr18:29869293..29870126-chr18:30132476..30133178,2	MCF-7	breast:
27	chr18:29737793..29738341-chr18:30132122..30132837,2	MCF-7	breast:
28	chr18:30124765..30126879-chr18:30130825..30132479,2	MCF-7	breast:
29	chr18:30188889..30190990-chr18:30209240..30211617,2	MCF-7	breast:
30	chr18:29737713..29738256-chr18:30129386..30129926,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC012123.1.1-3	chr18:30162577-30162791	ENSG00000263688.1
2	lnc-AC012123.1.1-3	chr18:30161491-30161539	ENSG00000263688.1

Variant related genes	Relation type
ENSG00000263688	TF binding region
ENSG00000141441	chromatin interactions

Extended variants
information (count: 1421 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1421 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs330980	chr18:30119207-30119208	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs528891675	chr18:30119215-30119216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs77467574	chr18:30119231-30119232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144156180	chr18:30119241-30119242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527951684	chr18:30119257-30119258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs59222526	chr18:30119264-30119265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570919206	chr18:30119301-30119302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538439621	chr18:30119327-30119328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139968338	chr18:30119363-30119364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568257993	chr18:30119397-30119398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569690293	chr18:30119421-30119422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368590830	chr18:30119429-30119430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34803681	chr18:30119442-30119443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535439554	chr18:30119472-30119473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553775908	chr18:30119474-30119475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs116428844	chr18:30119561-30119562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142814522	chr18:30119564-30119565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558041170	chr18:30119567-30119568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576109943	chr18:30119588-30119589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140836293	chr18:30119603-30119604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146086462	chr18:30119617-30119618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561277207	chr18:30119618-30119619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115844869	chr18:30119629-30119630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12959106	chr18:30119633-30119634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567128013	chr18:30119671-30119672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146054052	chr18:30119739-30119740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535986792	chr18:30119746-30119747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372147673	chr18:30119808-30119809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371161850	chr18:30119816-30119817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552550041	chr18:30119946-30119947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571173200	chr18:30119964-30119965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190746397	chr18:30119966-30119967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550663939	chr18:30119998-30119999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547296062	chr18:30120043-30120044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs549998877	chr18:30120053-30120054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182616599	chr18:30120110-30120111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535524555	chr18:30120154-30120155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs111471597	chr18:30120169-30120170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs117034265	chr18:30120197-30120198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564611088	chr18:30120863-30120864	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs151267043	chr18:30120889-30120890	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs550082104	chr18:30120920-30120921	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs78591986	chr18:30120933-30120934	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs139363671	chr18:30120958-30120959	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs72941784	chr18:30120971-30120972	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs187743671	chr18:30120972-30120973	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs575444563	chr18:30120982-30120983	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551786769	chr18:30121007-30121008	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570088461	chr18:30121016-30121017	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs112140500	chr18:30121027-30121028	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
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
Colorectal cancer	16272173	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
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
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	21811587	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:187 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30119200-30120200	Enhancers	Stomach Mucosa	stomach
2	chr18:30121800-30122600	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr18:30121800-30122600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr18:30121800-30122600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr18:30122000-30122600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr18:30122000-30122600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr18:30122000-30122600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr18:30122000-30122800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr18:30122200-30122600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr18:30122200-30122600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr18:30122200-30122600	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr18:30122200-30122600	Enhancers	Placenta	Placenta
13	chr18:30122600-30123400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr18:30122600-30126600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr18:30122600-30127800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr18:30122600-30133200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr18:30122800-30123200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr18:30123600-30123800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr18:30126600-30127400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr18:30127200-30127800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr18:30127400-30128600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr18:30127800-30128600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr18:30127800-30128800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr18:30128000-30130200	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr18:30128200-30128400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr18:30128200-30129000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr18:30128200-30129200	Enhancers	Fetal Intestine Small	intestine
28	chr18:30128200-30129800	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr18:30128200-30130000	Enhancers	H1 Cell Line	embryonic stem cell
30	chr18:30128400-30128600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr18:30128400-30128600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr18:30128400-30129000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr18:30128400-30129000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr18:30128400-30129200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
35	chr18:30128400-30129200	Enhancers	Fetal Intestine Large	intestine
36	chr18:30128400-30129400	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr18:30128400-30129800	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr18:30128600-30128800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr18:30128600-30129000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr18:30128600-30129000	Enhancers	H9 Cell Line	embryonic stem cell
41	chr18:30128600-30129000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr18:30128600-30129000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr18:30128600-30129000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr18:30128600-30129000	Enhancers	Fetal Heart	heart
45	chr18:30128600-30129000	Enhancers	Fetal Muscle Leg	muscle
46	chr18:30128600-30129000	Enhancers	Stomach Mucosa	stomach
47	chr18:30128600-30129200	Enhancers	Duodenum Mucosa	Duodenum
48	chr18:30128600-30130000	Enhancers	Fetal Brain Male	brain
49	chr18:30128600-30130200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr18:30128800-30131000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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