Variant report

Variant	nsv530515
Chromosome Location	chr18:24704459-24883897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:687)
CpG islands
(count:610)
Chromatin interactive
region (count:18)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:687 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	ARID3A	chr18:24818776-24818854	K562	blood:	n/a	n/a
3	ARID3A	chr18:24871931-24872131	K562	blood:	n/a	n/a
4	ARID3A	chr18:24777810-24778518	HepG2	liver:	n/a	n/a
5	ATF1	chr18:24820083-24820284	K562	blood:	n/a	n/a
6	ATF1	chr18:24868595-24868598	K562	blood:	n/a	n/a
7	ATF1	chr18:24818736-24818908	K562	blood:	n/a	n/a
8	ATF1	chr18:24763423-24763503	K562	blood:	n/a	n/a
9	ATF1	chr18:24779782-24779947	K562	blood:	n/a	n/a
10	ATF1	chr18:24761884-24761917	K562	blood:	n/a	n/a
11	ATF1	chr18:24815630-24815792	K562	blood:	n/a	n/a
12	ATF1	chr18:24784086-24784430	K562	blood:	n/a	n/a
13	ATF1	chr18:24807384-24807646	K562	blood:	n/a	n/a
14	ATF1	chr18:24830641-24830642	K562	blood:	n/a	n/a
15	ATF1	chr18:24827298-24827505	K562	blood:	n/a	n/a
16	ATF1	chr18:24875993-24876076	K562	blood:	n/a	n/a
17	ATF1	chr18:24874465-24874649	K562	blood:	n/a	n/a
18	ATF1	chr18:24822246-24822493	K562	blood:	n/a	n/a
19	ATF1	chr18:24761429-24761582	K562	blood:	n/a	n/a
20	ATF1	chr18:24707007-24707009	K562	blood:	n/a	n/a
21	ATF1	chr18:24833527-24833719	K562	blood:	n/a	n/a
22	ATF3	chr18:24716186-24716326	HepG2	liver:	n/a	n/a
23	BACH1	chr18:24765163-24765182	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr18:24709050-24709054	K562	blood:	n/a	n/a
25	BACH1	chr18:24764352-24764632	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr18:24842746-24842756	K562	blood:	n/a	n/a
27	BACH1	chr18:24779499-24779643	K562	blood:	n/a	n/a
28	BCL11A	chr18:24820443-24820728	GM12878	blood:	n/a	n/a
29	BHLHE40	chr18:24819169-24819170	K562	blood:	n/a	n/a
30	BHLHE40	chr18:24843619-24843771	K562	blood:	n/a	n/a
31	BHLHE40	chr18:24715587-24715933	GM12878	blood:	n/a	n/a
32	BHLHE40	chr18:24716111-24716471	HepG2	liver:	n/a	n/a
33	BHLHE40	chr18:24820205-24820821	GM12878	blood:	n/a	n/a
34	BHLHE40	chr18:24819115-24819311	GM12878	blood:	n/a	n/a
35	BHLHE40	chr18:24868968-24869139	K562	blood:	n/a	n/a
36	CBX3	chr18:24729202-24729532	K562	blood:	n/a	n/a
37	CCNT2	chr18:24877943-24878352	K562	blood:	n/a	n/a
38	CEBPB	chr18:24819695-24819939	HepG2	liver:	n/a	n/a
39	CEBPB	chr18:24716078-24716533	HepG2	liver:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
40	CEBPB	chr18:24716115-24716315	K562	blood:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
41	CEBPB	chr18:24778351-24778577	K562	blood:	n/a	chr18:24778467-24778484 chr18:24778470-24778483
42	CEBPB	chr18:24716143-24716486	HepG2	liver:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
43	CEBPB	chr18:24878324-24878647	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr18:24716075-24716429	Hela-S3	cervix:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
45	CEBPB	chr18:24716019-24716509	ECC-1	luminal epithelium:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
46	CEBPB	chr18:24715992-24716485	A549	lung:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
47	CEBPB	chr18:24716155-24716411	MCF-7	breast:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
48	CEBPB	chr18:24716122-24716427	A549	lung:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
49	CEBPB	chr18:24767247-24767461	HepG2	liver:	n/a	chr18:24767358-24767369 chr18:24767399-24767412
50	CEBPB	chr18:24774994-24775125	H1-hESC	embryonic stem cell:	n/a	chr18:24775040-24775051

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:24764599-24764649	T-47D	breast:	n/a
2	chr18:24765154-24765204	SAEC	small airway:	n/a
3	chr18:24765154-24765204	HAEpiC	amniotic membrane:	n/a
4	chr18:24765485-24765535	HL-60	blood:	n/a
5	chr18:24765490-24765540	HUVEC	blood vessel:	n/a
6	chr18:24765490-24765540	HCPEpiC	choroid plexus:	n/a
7	chr18:24765490-24765540	SK-N-SH	brain:	n/a
8	chr18:24765473-24765523	HCT-116	colon:	n/a
9	chr18:24764599-24764649	AG09309	skin:	n/a
10	chr18:24765781-24765831	HEEpiC	esophagus:	n/a
11	chr18:24765119-24765169	AG10803	skin:	n/a
12	chr18:24765781-24765831	NHBE	bronchial:	n/a
13	chr18:24765781-24765831	HCT-116	colon:	n/a
14	chr18:24765490-24765540	RPTEC	kidney:	n/a
15	chr18:24765643-24765693	AG09319	gingival:	n/a
16	chr18:24765781-24765831	HRPEpiC	eye:	n/a
17	chr18:24765643-24765693	HIPEpiC	eye:	n/a
18	chr18:24765154-24765204	HRE	kidney:	n/a
19	chr18:24762316-24762366	HCPEpiC	choroid plexus:	n/a
20	chr18:24765485-24765535	CMK	blood:	n/a
21	chr18:24762316-24762366	BE2_C	brain:	n/a
22	chr18:24765473-24765523	AG09309	skin:	n/a
23	chr18:24762316-24762366	HepG2	liver:	n/a
24	chr18:24765473-24765523	HL-60	blood:	n/a
25	chr18:24764966-24765016	HRPEpiC	eye:	n/a
26	chr18:24765781-24765831	GM12892	blood:	n/a
27	chr18:24765485-24765535	ProgFib	skin:	n/a
28	chr18:24765643-24765693	AG10803	skin:	n/a
29	chr18:24765154-24765204	NB4	blood:	n/a
30	chr18:24765485-24765535	SKMC	muscle:	n/a
31	chr18:24765490-24765540	HRCEpiC	kidney:	n/a
32	chr18:24764599-24764649	GM12892	blood:	n/a
33	chr18:24765119-24765169	NHBE	bronchial:	n/a
34	chr18:24765781-24765831	H1-hESC	embryonic stem cell:	embryo
35	chr18:24765485-24765535	Hepatocyte	liver:	n/a
36	chr18:24765119-24765169	Jurkat	blood:	n/a
37	chr18:24762316-24762366	PrEC	prostate:	n/a
38	chr18:24765643-24765693	HCT-116	colon:	n/a
39	chr18:24765485-24765535	HMEC	breast:	n/a
40	chr18:24765485-24765535	SAEC	small airway:	n/a
41	chr18:24764599-24764649	HCT-116	colon:	n/a
42	chr18:24765643-24765693	AG09309	skin:	n/a
43	chr18:24764599-24764649	AG10803	skin:	n/a
44	chr18:24765473-24765523	RPTEC	kidney:	n/a
45	chr18:24762316-24762366	NHBE	bronchial:	n/a
46	chr18:24765485-24765535	K562	blood:	n/a
47	chr18:24762316-24762366	AG10803	skin:	n/a
48	chr18:24764599-24764649	GM06990	blood:	n/a
49	chr18:24765490-24765540	H1-hESC	embryonic stem cell:	embryo
50	chr18:24765154-24765204	HIPEpiC	eye:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:24712355..24714811-chr18:24718073..24719662,2	MCF-7	breast:
2	chr18:24712355..24714811-chr18:24718073..24719662,2	MCF-7	breast:
3	chr18:24734168..24736128-chr18:24762446..24765149,2	K562	blood:
4	chr18:24770863..24773354-chr18:24775315..24777406,2	K562	blood:
5	chr18:24754408..24756988-chr18:24763307..24765193,2	K562	blood:
6	chr18:24734168..24736128-chr18:24762446..24765149,2	K562	blood:
7	chr18:24597605..24598649-chr18:24878090..24879048,4	MCF-7	breast:
8	chr18:24587162..24589841-chr18:24735427..24737669,2	K562	blood:
9	chr18:24744878..24747343-chr18:24750374..24752456,2	K562	blood:
10	chr18:24744878..24747343-chr18:24750374..24752456,2	K562	blood:
11	chr18:24816860..24819247-chr18:24819852..24822725,2	K562	blood:
12	chr1:240408331..240409076-chr18:24854645..24855291,2	MCF-7	breast:
13	chr18:24836460..24838424-chr18:24839356..24841492,2	K562	blood:
14	chr14:56390153..56391038-chr18:24814712..24815423,2	MCF-7	breast:
15	chr18:24816860..24819247-chr18:24819852..24822725,2	K562	blood:
16	chr18:24770863..24773354-chr18:24775315..24777406,2	K562	blood:
17	chr18:24836460..24838424-chr18:24839356..24841492,2	K562	blood:
18	chr18:24754408..24756988-chr18:24763307..24765193,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAF4B-5	chr18:24827005-24827152	ENSG00000265374.1
2	lnc-TAF4B-5	chr18:24815572-24815623	ENSG00000265374.1
3	lnc-TAF4B-4	chr18:24727662-24727742	ENSG00000260372.2
4	lnc-TAF4B-5	chr18:24823577-24823630	ENSG00000265374.1
5	lnc-TAF4B-4	chr18:24768707-24770662	ENSG00000260372.2
6	lnc-TAF4B-5	chr18:24805706-24805925	ENSG00000265374.1
7	lnc-TAF4B-5	chr18:24814886-24814966	ENSG00000265374.1

No data

Variant related genes	Relation type
ENSG00000265374	TF binding region
CHST9	TF binding region
ENSG00000265374	CpG island
CHST9	CpG island
ENSG00000155816	chromatin interactions

Extended variants
information (count: 4918 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4918 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569989566	chr18:24704484-24704485	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186812379	chr18:24704498-24704499	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549450183	chr18:24704544-24704545	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144715604	chr18:24704549-24704550	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12958230	chr18:24704597-24704598	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs147467233	chr18:24704645-24704646	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577924707	chr18:24704665-24704666	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192119314	chr18:24704684-24704685	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116589074	chr18:24704685-24704686	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557515121	chr18:24704686-24704687	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9960062	chr18:24704696-24704697	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs9959436	chr18:24704712-24704713	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs9951527	chr18:24704757-24704758	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs573624553	chr18:24704769-24704770	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116731696	chr18:24704812-24704813	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559550159	chr18:24704819-24704820	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144544059	chr18:24704834-24704835	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11873301	chr18:24704846-24704847	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145650398	chr18:24704854-24704855	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181927955	chr18:24704855-24704856	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9949069	chr18:24704884-24704885	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs555115452	chr18:24704890-24704891	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549239121	chr18:24704891-24704892	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566953668	chr18:24704897-24704898	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs16943302	chr18:24704978-24704979	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs9954010	chr18:24705067-24705068	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs546792360	chr18:24705086-24705087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571503717	chr18:24705121-24705122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559134463	chr18:24705163-24705164	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35985681	chr18:24705168-24705169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531392902	chr18:24705216-24705217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577306328	chr18:24705238-24705239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371121422	chr18:24705250-24705251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186581581	chr18:24705293-24705294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575972815	chr18:24705309-24705310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs28626613	chr18:24705337-24705338	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs555026707	chr18:24705405-24705406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573787934	chr18:24705419-24705420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541082136	chr18:24705425-24705426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553253048	chr18:24705440-24705441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs34853800	chr18:24705448-24705449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544646595	chr18:24705454-24705455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs28658184	chr18:24705501-24705502	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs545358313	chr18:24705502-24705503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563577628	chr18:24705516-24705517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557277629	chr18:24705542-24705543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189801293	chr18:24705568-24705569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543024457	chr18:24705571-24705572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542580074	chr18:24705583-24705584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182411762	chr18:24705676-24705677	Enhancers Weak transcription	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	22037309	CNVD

Chromatin state (count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24693600-24707200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr18:24698800-24715600	Weak transcription	Pancreas	Pancrea
3	chr18:24702600-24709800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr18:24703600-24705000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr18:24703600-24705000	Enhancers	H1 Cell Line	embryonic stem cell
6	chr18:24703600-24705000	Enhancers	H9 Cell Line	embryonic stem cell
7	chr18:24703600-24705800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr18:24703800-24705000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr18:24703800-24705800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr18:24703800-24706800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr18:24704000-24704800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr18:24704200-24704600	Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr18:24704200-24704600	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr18:24704400-24705000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr18:24704600-24704800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
16	chr18:24704600-24704800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr18:24704800-24705400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr18:24704800-24705800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr18:24704800-24706000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr18:24704800-24709400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr18:24705000-24706400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr18:24705000-24709800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr18:24705400-24709800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr18:24705800-24709600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr18:24705800-24709600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr18:24705800-24709800	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr18:24706000-24709600	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr18:24706000-24715600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr18:24706200-24706800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr18:24706400-24709600	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr18:24706800-24709800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr18:24706800-24710400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr18:24707200-24708000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr18:24708000-24715400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr18:24709400-24710000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr18:24709400-24710400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr18:24709600-24710400	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr18:24709600-24710400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr18:24709600-24710400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr18:24709600-24710400	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr18:24709800-24710200	Enhancers	H1 Cell Line	embryonic stem cell
42	chr18:24709800-24710200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr18:24709800-24710400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr18:24709800-24710600	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr18:24709800-24710600	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr18:24710000-24710200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr18:24710000-24715800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr18:24710200-24710400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr18:24710200-24711000	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr18:24710200-24717800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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