Variant report

Variant	nsv1066906
Chromosome Location	chr18:30125366-30192567
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	chr18:30129239-30129485	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:30131174-30131190	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:30142422-30142500	HepG2	liver:	n/a	n/a
4	BACH1	chr18:30190420-30190421	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr18:30178218-30178457	GM12878	blood:	n/a	n/a
6	BCL11A	chr18:30128823-30129068	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr18:30128823-30129054	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr18:30132459-30132771	GM12878	blood:	n/a	n/a
9	BHLHE40	chr18:30129259-30129459	GM12878	blood:	n/a	n/a
10	CEBPB	chr18:30146615-30146815	A549	lung:	n/a	n/a
11	CEBPB	chr18:30141181-30141299	HepG2	liver:	n/a	chr18:30141235-30141246
12	CEBPB	chr18:30157855-30158133	IMR90	lung:	n/a	chr18:30157971-30157982
13	CEBPB	chr18:30159138-30159403	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr18:30157849-30158073	HepG2	liver:	n/a	chr18:30157971-30157982
15	CHD2	chr18:30136205-30136420	K562	blood:	n/a	n/a
16	CHD2	chr18:30130908-30131239	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr18:30132430-30132793	HepG2	liver:	n/a	n/a
18	CREB1	chr18:30129332-30129474	A549	lung:	n/a	chr18:30129418-30129431
19	CREB1	chr18:30129310-30129517	H1-hESC	embryonic stem cell:	n/a	chr18:30129418-30129431
20	CREB1	chr18:30129211-30129650	H1-hESC	embryonic stem cell:	n/a	chr18:30129418-30129431
21	CREB1	chr18:30129311-30129495	A549	lung:	n/a	chr18:30129418-30129431
22	CTCF	chr18:30132480-30132630	GM12867	blood:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
23	CTCF	chr18:30131017-30131154	H1-hESC	embryonic stem cell:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
24	CTCF	chr18:30132520-30132670	HepG2	liver:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
25	CTCF	chr18:30156393-30156478	GM10266	blood:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
26	CTCF	chr18:30132820-30132970	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr18:30129308-30129503	GM13976	blood:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
28	CTCF	chr18:30129320-30129470	HPAF	blood vessel:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
29	CTCF	chr18:30129300-30129450	GM12865	blood:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
30	CTCF	chr18:30156377-30156515	GM12878	blood:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
31	CTCF	chr18:30131060-30131210	HCM	heart:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
32	CTCF	chr18:30129320-30129470	GM12866	blood:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
33	CTCF	chr18:30132306-30132856	MCF-7	breast:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
34	CTCF	chr18:30156350-30156543	Spleen_OC	spleen:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
35	CTCF	chr18:30131000-30131150	HepG2	liver:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
36	CTCF	chr18:30132493-30132701	GM10248	blood:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
37	CTCF	chr18:30156313-30156540	HUVEC	blood vessel:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
38	CTCF	chr18:30129340-30129490	Hela-S3	cervix:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
39	CTCF	chr18:30129294-30129519	MCF-7	breast:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
40	CTCF	chr18:30132450-30132710	HepG2	liver:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
41	CTCF	chr18:30129242-30129499	K562	blood:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
42	CTCF	chr18:30132460-30132706	ECC-1	luminal epithelium:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
43	CTCF	chr18:30130960-30131110	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr18:30132940-30133090	GM12865	blood:	n/a	n/a
45	CTCF	chr18:30129360-30129510	GM12866	blood:	n/a	chr18:30129403-30129416 chr18:30129400-30129413 chr18:30129398-30129416 chr18:30129404-30129413 chr18:30129393-30129414
46	CTCF	chr18:30131040-30131190	NHEK	skin:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
47	CTCF	chr18:30156280-30156430	BJ	skin:	n/a	n/a
48	CTCF	chr18:30175820-30175970	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr18:30131000-30131150	HA-sp	spinal cord:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
50	CTCF	chr18:30132540-30132690	GM12873	blood:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594

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

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

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

Extended variants
information (count: 1178 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1178 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111397712	chr18:30125406-30125407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570355705	chr18:30125407-30125408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147943493	chr18:30125431-30125432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531461681	chr18:30125435-30125436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543562588	chr18:30125491-30125492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187850860	chr18:30125511-30125512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140105049	chr18:30125544-30125545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150295346	chr18:30125559-30125560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs55708663	chr18:30125571-30125572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369952628	chr18:30125599-30125600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548597909	chr18:30125620-30125621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191879807	chr18:30125693-30125694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527866959	chr18:30125708-30125709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552384093	chr18:30125735-30125736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528181838	chr18:30125743-30125744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184363303	chr18:30125844-30125845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537916037	chr18:30125853-30125854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549874375	chr18:30125877-30125878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568069508	chr18:30125903-30125904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535886378	chr18:30125920-30125921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553771038	chr18:30125935-30125936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538110583	chr18:30126007-30126008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572336854	chr18:30126023-30126024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546336988	chr18:30126024-30126025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs115076165	chr18:30126080-30126081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557955112	chr18:30126185-30126186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576319338	chr18:30126197-30126198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543501246	chr18:30126247-30126248	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs188526572	chr18:30126254-30126255	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs570890166	chr18:30126307-30126308	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs74664625	chr18:30126335-30126336	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs144973931	chr18:30126349-30126350	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111725643	chr18:30126373-30126374	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs201710850	chr18:30126400-30126401	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs143150603	chr18:30126417-30126418	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs4799649	chr18:30126466-30126467	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs80031371	chr18:30126476-30126477	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531794580	chr18:30126478-30126479	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138688607	chr18:30126484-30126485	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs568578387	chr18:30126499-30126500	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535463133	chr18:30126505-30126506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs547795699	chr18:30126534-30126535	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs565960524	chr18:30126581-30126582	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs539709350	chr18:30126588-30126589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs558092638	chr18:30126602-30126603	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192901838	chr18:30126615-30126616	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537282878	chr18:30126648-30126649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs78737555	chr18:30126655-30126656	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs147083573	chr18:30126663-30126664	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs573708990	chr18:30126664-30126665	Weak transcription Enhancers	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:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30122600-30126600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr18:30122600-30127800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr18:30122600-30133200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr18:30126600-30127400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr18:30127200-30127800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr18:30127400-30128600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr18:30127800-30128600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr18:30127800-30128800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr18:30128000-30130200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr18:30128200-30128400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr18:30128200-30129000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr18:30128200-30129200	Enhancers	Fetal Intestine Small	intestine
13	chr18:30128200-30129800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr18:30128200-30130000	Enhancers	H1 Cell Line	embryonic stem cell
15	chr18:30128400-30128600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr18:30128400-30128600	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr18:30128400-30129000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr18:30128400-30129000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr18:30128400-30129200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
20	chr18:30128400-30129200	Enhancers	Fetal Intestine Large	intestine
21	chr18:30128400-30129400	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr18:30128400-30129800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr18:30128600-30128800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr18:30128600-30129000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr18:30128600-30129000	Enhancers	H9 Cell Line	embryonic stem cell
26	chr18:30128600-30129000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr18:30128600-30129000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr18:30128600-30129000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr18:30128600-30129000	Enhancers	Fetal Heart	heart
30	chr18:30128600-30129000	Enhancers	Fetal Muscle Leg	muscle
31	chr18:30128600-30129000	Enhancers	Stomach Mucosa	stomach
32	chr18:30128600-30129200	Enhancers	Duodenum Mucosa	Duodenum
33	chr18:30128600-30130000	Enhancers	Fetal Brain Male	brain
34	chr18:30128600-30130200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr18:30128800-30131000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr18:30128800-30133000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr18:30129000-30129800	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr18:30129000-30129800	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr18:30129000-30129800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr18:30129000-30131000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr18:30129000-30131200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr18:30129000-30132400	Weak transcription	Stomach Mucosa	stomach
43	chr18:30129000-30133600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr18:30129200-30130200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr18:30129200-30132800	Weak transcription	Fetal Intestine Small	intestine
46	chr18:30129800-30130800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr18:30129800-30130800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr18:30129800-30130800	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr18:30129800-30130800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr18:30129800-30130800	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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