Variant report

Variant	nsv1067103
Chromosome Location	chr18:24524011-24760469
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1273)
CpG islands
(count:61)
Chromatin interactive
region (count:32)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1273 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:24597977-24598176	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:24641618-24642040	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:24722857-24723286	HepG2	liver:	n/a	n/a
4	ATF1	chr18:24680024-24680135	K562	blood:	n/a	n/a
5	ATF1	chr18:24668979-24668983	K562	blood:	n/a	n/a
6	ATF1	chr18:24610955-24610984	K562	blood:	n/a	n/a
7	ATF1	chr18:24663203-24663207	K562	blood:	n/a	n/a
8	ATF1	chr18:24692205-24692289	K562	blood:	n/a	n/a
9	ATF1	chr18:24707007-24707009	K562	blood:	n/a	n/a
10	ATF2	chr18:24653219-24653861	GM12878	blood:	n/a	n/a
11	ATF2	chr18:24653235-24653878	GM12878	blood:	n/a	n/a
12	ATF2	chr18:24558928-24559377	GM12878	blood:	n/a	n/a
13	ATF2	chr18:24558816-24559341	GM12878	blood:	n/a	n/a
14	ATF3	chr18:24716186-24716326	HepG2	liver:	n/a	n/a
15	BACH1	chr18:24709050-24709054	K562	blood:	n/a	n/a
16	BACH1	chr18:24702204-24702331	K562	blood:	n/a	n/a
17	BATF	chr18:24653243-24653721	GM12878	blood:	n/a	chr18:24653467-24653480
18	BATF	chr18:24558684-24558944	GM12878	blood:	n/a	n/a
19	BCL11A	chr18:24536879-24537112	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL11A	chr18:24536886-24537213	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr18:24653235-24653781	GM12878	blood:	n/a	chr18:24653410-24653419
22	BCL11A	chr18:24558970-24559271	GM12878	blood:	n/a	n/a
23	BCL11A	chr18:24653240-24653552	GM12878	blood:	n/a	chr18:24653410-24653419
24	BCL3	chr18:24653281-24653600	GM12878	blood:	n/a	chr18:24653410-24653419
25	BCLAF1	chr18:24585578-24585881	GM12878	blood:	n/a	n/a
26	BHLHE40	chr18:24716111-24716471	HepG2	liver:	n/a	n/a
27	BHLHE40	chr18:24715587-24715933	GM12878	blood:	n/a	n/a
28	BHLHE40	chr18:24558451-24559307	GM12878	blood:	n/a	n/a
29	BHLHE40	chr18:24641514-24641793	HepG2	liver:	n/a	n/a
30	BHLHE40	chr18:24557899-24558066	GM12878	blood:	n/a	n/a
31	BHLHE40	chr18:24597908-24598105	GM12878	blood:	n/a	n/a
32	BHLHE40	chr18:24658700-24658716	K562	blood:	n/a	n/a
33	BHLHE40	chr18:24653404-24653604	GM12878	blood:	n/a	n/a
34	BHLHE40	chr18:24641394-24642038	HepG2	liver:	n/a	n/a
35	CBX3	chr18:24729202-24729532	K562	blood:	n/a	n/a
36	CCNT2	chr18:24604223-24604391	K562	blood:	n/a	n/a
37	CCNT2	chr18:24647874-24648076	K562	blood:	n/a	n/a
38	CCNT2	chr18:24622103-24622165	K562	blood:	n/a	n/a
39	CEBPB	chr18:24666103-24666319	HepG2	liver:	n/a	chr18:24666146-24666157
40	CEBPB	chr18:24716078-24716533	HepG2	liver:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
41	CEBPB	chr18:24602546-24602660	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr18:24560487-24560519	HepG2	liver:	n/a	n/a
43	CEBPB	chr18:24579009-24579284	K562	blood:	n/a	chr18:24579111-24579122 chr18:24579110-24579123 chr18:24579110-24579121 chr18:24579112-24579121
44	CEBPB	chr18:24641413-24642030	HepG2	liver:	n/a	chr18:24641584-24641595
45	CEBPB	chr18:24628882-24629128	HepG2	liver:	n/a	chr18:24629051-24629064
46	CEBPB	chr18:24716115-24716315	K562	blood:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
47	CEBPB	chr18:24543836-24544029	IMR90	lung:	n/a	chr18:24543940-24543951
48	CEBPB	chr18:24716125-24716411	IMR90	lung:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
49	CEBPB	chr18:24641567-24641771	IMR90	lung:	n/a	chr18:24641584-24641595
50	CEBPB	chr18:24641407-24642057	HepG2	liver:	n/a	chr18:24641584-24641595

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:24537063-24537113	GM19239	blood:	n/a
2	chr18:24537063-24537113	SK-N-SH	brain:	n/a
3	chr18:24537063-24537113	AG09319	gingival:	n/a
4	chr18:24537063-24537113	AG04449	skin:	fetal
5	chr18:24537063-24537113	HCF	heart:	n/a
6	chr18:24537063-24537113	NHDF-neo	bronchial:	n/a
7	chr18:24537063-24537113	U87	brain:	n/a
8	chr18:24537063-24537113	BJ	skin:	n/a
9	chr18:24537063-24537113	HEK293	kidney:	embryo
10	chr18:24537063-24537113	Hepatocyte	liver:	n/a
11	chr18:24537063-24537113	BE2_C	brain:	n/a
12	chr18:24537063-24537113	HUVEC	blood vessel:	n/a
13	chr18:24537063-24537113	SK-N-SH_RA	brain:	n/a
14	chr18:24537063-24537113	SAEC	small airway:	n/a
15	chr18:24537063-24537113	GM12878	blood:	n/a
16	chr18:24537063-24537113	K562	blood:	n/a
17	chr18:24537063-24537113	ProgFib	skin:	n/a
18	chr18:24537063-24537113	AG10803	skin:	n/a
19	chr18:24537063-24537113	HMEC	breast:	n/a
20	chr18:24537063-24537113	Hela-S3	cervix:	n/a
21	chr18:24537063-24537113	PANC-1	pancreas:	n/a
22	chr18:24537063-24537113	HCM	heart:	n/a
23	chr18:24537063-24537113	HRPEpiC	eye:	n/a
24	chr18:24537063-24537113	AoSMC	blood vessel:	n/a
25	chr18:24537063-24537113	Caco-2	colon:	n/a
26	chr18:24537063-24537113	HCPEpiC	choroid plexus:	n/a
27	chr18:24537063-24537113	HCT-116	colon:	n/a
28	chr18:24537063-24537113	HL-60	blood:	n/a
29	chr18:24537063-24537113	HNPCEpiC	eye:	n/a
30	chr18:24537063-24537113	IMR90	lung:	fetal
31	chr18:24537063-24537113	HRCEpiC	kidney:	n/a
32	chr18:24537063-24537113	HPAEpiC	pulmonary alveolar:	n/a
33	chr18:24537063-24537113	ovcar-3	ovarian:	n/a
34	chr18:24537063-24537113	NH-A	brain:	n/a
35	chr18:24537063-24537113	LNCaP	prostate:	n/a
36	chr18:24537063-24537113	PrEC	prostate:	n/a
37	chr18:24537063-24537113	AG04450	lung:	fetal
38	chr18:24537063-24537113	GM06990	blood:	n/a
39	chr18:24537063-24537113	HAEpiC	amniotic membrane:	n/a
40	chr18:24537063-24537113	NHBE	bronchial:	n/a
41	chr18:24537063-24537113	A549	lung:	n/a
42	chr18:24537063-24537113	ECC-1	luminal epithelium:	n/a
43	chr18:24537063-24537113	HRE	kidney:	n/a
44	chr18:24537063-24537113	HEEpiC	esophagus:	n/a
45	chr18:24537063-24537113	H1-hESC	embryonic stem cell:	embryo
46	chr18:24537063-24537113	GM12891	blood:	n/a
47	chr18:24537063-24537113	NT2-D1	testis:	n/a
48	chr18:24537063-24537113	MCF10A-Er-Src	breast:	n/a
49	chr18:24537063-24537113	HIPEpiC	eye:	n/a
50	chr18:24537063-24537113	RPTEC	kidney:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:57915136..57916681-chr18:24622286..24624382,2	MCF-7	breast:
2	chr18:24712355..24714811-chr18:24718073..24719662,2	MCF-7	breast:
3	chr18:24754408..24756988-chr18:24763307..24765193,2	K562	blood:
4	chr18:24563994..24566667-chr18:24568829..24570336,2	K562	blood:
5	chr18:24590450..24592639-chr18:24595397..24598206,2	K562	blood:
6	chr18:24734168..24736128-chr18:24762446..24765149,2	K562	blood:
7	chr18:24392717..24393537-chr18:24585343..24586051,3	MCF-7	breast:
8	chr18:24590450..24592639-chr18:24595397..24598206,2	K562	blood:
9	chr18:24744878..24747343-chr18:24750374..24752456,2	K562	blood:
10	chr18:24558208..24560365-chr18:24586834..24589687,2	K562	blood:
11	chr18:24654215..24656527-chr18:24658995..24661475,2	K562	blood:
12	chr18:24744878..24747343-chr18:24750374..24752456,2	K562	blood:
13	chr18:24385096..24386862-chr18:24541525..24543667,2	MCF-7	breast:
14	chr18:24587162..24589841-chr18:24735427..24737669,2	K562	blood:
15	chr18:24712355..24714811-chr18:24718073..24719662,2	MCF-7	breast:
16	chr18:24574463..24577146-chr18:24577247..24578836,2	K562	blood:
17	chr18:24392703..24393679-chr18:24542716..24543961,5	MCF-7	breast:
18	chr18:24574463..24577146-chr18:24577247..24578836,2	K562	blood:
19	chr18:24654215..24656527-chr18:24658995..24661475,2	K562	blood:
20	chr18:24392850..24393920-chr18:24583781..24585072,6	MCF-7	breast:
21	chr18:24392758..24393709-chr18:24584107..24584615,2	MCF-7	breast:
22	chr18:24622509..24625016-chr18:24625239..24626896,2	MCF-7	breast:
23	chr18:24597605..24598649-chr18:24878090..24879048,4	MCF-7	breast:
24	chr18:24564837..24566667-chr18:24568829..24570386,2	K562	blood:
25	chr18:24598008..24598574-chr18:25195967..25196583,2	MCF-7	breast:
26	chr18:24622509..24625016-chr18:24625239..24626896,2	MCF-7	breast:
27	chr18:24558208..24560365-chr18:24586834..24589687,2	K562	blood:
28	chr18:24563994..24566667-chr18:24568829..24570336,2	K562	blood:
29	chr18:24587162..24589841-chr18:24735427..24737669,2	K562	blood:
30	chr18:24598911..24600419-chr18:24602103..24604133,2	K562	blood:
31	chr18:24564837..24566667-chr18:24568829..24570386,2	K562	blood:
32	chr18:24598911..24600419-chr18:24602103..24604133,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAF4B-4	chr18:24727662-24727742	ENSG00000260372.2
2	lnc-AQP4-3	chr18:24532165-24532522	NONHSAT058769

No data

Variant related genes	Relation type
ENSG00000266549	TF binding region
CHST9	TF binding region
ENSG00000266549	CpG island
CHST9	CpG island
ENSG00000062716	chromatin interactions

Extended variants
information (count: 8420 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:8420 , 50 per page) page: 1 2 3 4 5 6 7 ... 169

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562344492	chr18:24524032-24524033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs117546954	chr18:24524067-24524068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs71353414	chr18:24524088-24524089	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs71353415	chr18:24524123-24524124	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs527452474	chr18:24524126-24524127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552500532	chr18:24524243-24524244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570683691	chr18:24524245-24524246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372748660	chr18:24524264-24524265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375766849	chr18:24524269-24524270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376266875	chr18:24524344-24524345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550195082	chr18:24524350-24524351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541031	chr18:24524421-24524422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568340443	chr18:24524431-24524432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535587750	chr18:24524469-24524470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553820931	chr18:24524481-24524482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs80002981	chr18:24524497-24524498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373955648	chr18:24524517-24524518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554292108	chr18:24524522-24524523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539605066	chr18:24524523-24524524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369784372	chr18:24524524-24524525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531125593	chr18:24524530-24524531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs16943019	chr18:24524561-24524562	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs576721663	chr18:24524628-24524629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181918200	chr18:24524676-24524677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556161079	chr18:24524734-24524735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs80258747	chr18:24524774-24524775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574454794	chr18:24524787-24524788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372300304	chr18:24524850-24524851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs78117014	chr18:24524905-24524906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560241790	chr18:24524937-24524938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs12954099	chr18:24524941-24524942	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs546018317	chr18:24524992-24524993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550191402	chr18:24525002-24525003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564122447	chr18:24525027-24525028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186955136	chr18:24525059-24525060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs549791128	chr18:24525068-24525069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568463871	chr18:24525111-24525112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs16943023	chr18:24525119-24525120	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs546578222	chr18:24525132-24525133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150494922	chr18:24525137-24525138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190586141	chr18:24525154-24525155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539545350	chr18:24525197-24525198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558360562	chr18:24525205-24525206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1683481	chr18:24525291-24525292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570174258	chr18:24525297-24525298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1786618	chr18:24525307-24525308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570137440	chr18:24525310-24525311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs1622078	chr18:24525330-24525331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs1786619	chr18:24525360-24525361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537768070	chr18:24525381-24525382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute myeloid leukemia	19651600	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:849 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24505400-24527200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr18:24508400-24529000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr18:24508600-24536800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr18:24521800-24524600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr18:24523200-24524200	Enhancers	Dnd41	blood
6	chr18:24524000-24524200	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr18:24524000-24524200	Weak transcription	HMEC	breast
8	chr18:24524000-24525400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr18:24524400-24524600	Enhancers	Colon Smooth Muscle	Colon
10	chr18:24524600-24525200	Weak transcription	Colon Smooth Muscle	Colon
11	chr18:24524600-24526400	Enhancers	Rectal Smooth Muscle	rectum
12	chr18:24525200-24526200	Enhancers	Colon Smooth Muscle	Colon
13	chr18:24525400-24526400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr18:24527200-24527800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
15	chr18:24527800-24536600	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr18:24528400-24529000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr18:24529000-24529200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr18:24529000-24529800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr18:24529200-24529600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr18:24529400-24529800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr18:24529600-24530000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr18:24529600-24530200	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr18:24529800-24530000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr18:24530000-24535400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr18:24530200-24535400	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr18:24532000-24532200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr18:24532200-24536800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr18:24535400-24535600	Weak transcription	Pancreas	Pancrea
29	chr18:24535400-24536000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr18:24535400-24536000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr18:24535600-24535800	Enhancers	Pancreas	Pancrea
32	chr18:24536000-24536400	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr18:24536000-24536400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr18:24536400-24536600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr18:24536400-24537800	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr18:24536600-24536800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr18:24536600-24536800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr18:24536600-24536800	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr18:24536600-24537000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr18:24536600-24537200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr18:24536600-24537200	Enhancers	Primary hematopoietic stem cells	blood
42	chr18:24536600-24537400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr18:24536600-24537600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr18:24536600-24537600	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr18:24536600-24538600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr18:24536800-24537000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr18:24536800-24537000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr18:24536800-24537000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
49	chr18:24536800-24537200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr18:24536800-24537200	Enhancers	Fetal Brain Female	brain

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