Variant report

Variant	nsv909476
Chromosome Location	chr18:24722839-24779601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:246)
CpG islands
(count:610)
Chromatin interactive
region (count:9)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:246 , 50 per page) page: 1 2 3 4 5

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	chr18:24777810-24778518	HepG2	liver:	n/a	n/a
3	ATF1	chr18:24763423-24763503	K562	blood:	n/a	n/a
4	ATF1	chr18:24761884-24761917	K562	blood:	n/a	n/a
5	ATF1	chr18:24761429-24761582	K562	blood:	n/a	n/a
6	BACH1	chr18:24779499-24779643	K562	blood:	n/a	n/a
7	BACH1	chr18:24764352-24764632	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr18:24765163-24765182	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr18:24729202-24729532	K562	blood:	n/a	n/a
10	CEBPB	chr18:24774998-24775161	K562	blood:	n/a	chr18:24775040-24775051
11	CEBPB	chr18:24767247-24767461	HepG2	liver:	n/a	chr18:24767358-24767369 chr18:24767399-24767412
12	CEBPB	chr18:24778351-24778577	K562	blood:	n/a	chr18:24778467-24778484 chr18:24778470-24778483
13	CEBPB	chr18:24774994-24775125	H1-hESC	embryonic stem cell:	n/a	chr18:24775040-24775051
14	CEBPB	chr18:24777826-24778604	HepG2	liver:	n/a	chr18:24778467-24778484 chr18:24778470-24778483
15	CEBPB	chr18:24774989-24775189	HepG2	liver:	n/a	chr18:24775040-24775051
16	CEBPB	chr18:24775015-24775170	A549	lung:	n/a	chr18:24775040-24775051
17	CTBP2	chr18:24764215-24765120	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr18:24743220-24743370	GM12875	blood:	n/a	n/a
19	CTCF	chr18:24743260-24743410	GM12869	blood:	n/a	n/a
20	CTCF	chr18:24743220-24743370	HepG2	liver:	n/a	n/a
21	CTCF	chr18:24743240-24743390	MCF-7	breast:	n/a	n/a
22	CTCF	chr18:24743260-24743410	GM12867	blood:	n/a	n/a
23	CTCF	chr18:24743284-24743490	MCF-7	breast:	n/a	n/a
24	CTCF	chr18:24743260-24743410	GM12871	blood:	n/a	n/a
25	CTCF	chr18:24743240-24743390	GM12878	blood:	n/a	n/a
26	CTCF	chr18:24743300-24743450	GM12864	blood:	n/a	n/a
27	CTCF	chr18:24743340-24743490	GM12878	blood:	n/a	n/a
28	CTCF	chr18:24743260-24743410	HMEC	breast:	n/a	n/a
29	CTCF	chr18:24743220-24743370	HEK293	kidney:	n/a	n/a
30	CTCF	chr18:24743260-24743410	GM12872	blood:	n/a	n/a
31	CTCF	chr18:24765517-24765538	LNCaP	prostate:	n/a	n/a
32	CTCF	chr18:24743274-24743489	MCF-7	breast:	n/a	n/a
33	CTCF	chr18:24743373-24743384	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr18:24764385-24764421	NHEK	skin:	n/a	n/a
35	CTCF	chr18:24743286-24743487	MCF-7	breast:	n/a	n/a
36	CTCF	chr18:24743260-24743410	HCT-116	colon:	n/a	n/a
37	CTCF	chr18:24743276-24743460	Gliobla	brain:	n/a	n/a
38	CTCF	chr18:24761660-24761810	RPTEC	kidney:	n/a	n/a
39	CTCF	chr18:24743260-24743410	A549	lung:	n/a	n/a
40	CTCF	chr18:24743260-24743410	RPTEC	kidney:	n/a	n/a
41	CTCF	chr18:24743300-24743444	GM19238	blood:	n/a	n/a
42	CTCF	chr18:24743220-24743370	GM06990	blood:	n/a	n/a
43	CTCF	chr18:24757601-24757614	K562	blood:	n/a	n/a
44	CTCF	chr18:24743220-24743370	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr18:24743220-24743370	GM12873	blood:	n/a	n/a
46	CTCF	chr18:24743260-24743410	MCF-7	breast:	n/a	n/a
47	CTCF	chr18:24743520-24743670	GM12868	blood:	n/a	n/a
48	CTCF	chr18:24743303-24743398	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr18:24743280-24743430	GM12872	blood:	n/a	n/a
50	CTCF	chr18:24765460-24765610	NHEK	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:24765490-24765540	Jurkat	blood:	n/a
2	chr18:24764599-24764649	SAEC	small airway:	n/a
3	chr18:24765781-24765831	RPTEC	kidney:	n/a
4	chr18:24765154-24765204	ECC-1	luminal epithelium:	n/a
5	chr18:24765643-24765693	SKMC	muscle:	n/a
6	chr18:24762316-24762366	HL-60	blood:	n/a
7	chr18:24765643-24765693	HCM	heart:	n/a
8	chr18:24765781-24765831	SKMC	muscle:	n/a
9	chr18:24762316-24762366	HIPEpiC	eye:	n/a
10	chr18:24765119-24765169	MCF-7	breast:	n/a
11	chr18:24765119-24765169	SAEC	small airway:	n/a
12	chr18:24765473-24765523	SK-N-MC	brain:	n/a
13	chr18:24765473-24765523	AG04449	skin:	fetal
14	chr18:24765473-24765523	T-47D	breast:	n/a
15	chr18:24765781-24765831	HRCEpiC	kidney:	n/a
16	chr18:24765643-24765693	NT2-D1	testis:	n/a
17	chr18:24764966-24765016	HAEpiC	amniotic membrane:	n/a
18	chr18:24765485-24765535	RPTEC	kidney:	n/a
19	chr18:24762316-24762366	GM12878	blood:	n/a
20	chr18:24764966-24765016	HMEC	breast:	n/a
21	chr18:24765485-24765535	CMK	blood:	n/a
22	chr18:24762316-24762366	HEEpiC	esophagus:	n/a
23	chr18:24765485-24765535	HIPEpiC	eye:	n/a
24	chr18:24765781-24765831	ECC-1	luminal epithelium:	n/a
25	chr18:24764966-24765016	MCF-7	breast:	n/a
26	chr18:24765781-24765831	NB4	blood:	n/a
27	chr18:24765485-24765535	GM12878	blood:	n/a
28	chr18:24765781-24765831	GM06990	blood:	n/a
29	chr18:24765485-24765535	K562	blood:	n/a
30	chr18:24765473-24765523	BE2_C	brain:	n/a
31	chr18:24764966-24765016	HRPEpiC	eye:	n/a
32	chr18:24765473-24765523	HCPEpiC	choroid plexus:	n/a
33	chr18:24765485-24765535	T-47D	breast:	n/a
34	chr18:24765490-24765540	AoSMC	blood vessel:	n/a
35	chr18:24765485-24765535	NHDF-neo	bronchial:	n/a
36	chr18:24765154-24765204	HPAEpiC	pulmonary alveolar:	n/a
37	chr18:24765490-24765540	HAEpiC	amniotic membrane:	n/a
38	chr18:24764966-24765016	ECC-1	luminal epithelium:	n/a
39	chr18:24765485-24765535	PFSK-1	brain:	n/a
40	chr18:24765643-24765693	SK-N-SH	brain:	n/a
41	chr18:24765473-24765523	SK-N-SH_RA	brain:	n/a
42	chr18:24764966-24765016	HEK293	kidney:	embryo
43	chr18:24765781-24765831	HMEC	breast:	n/a
44	chr18:24764966-24765016	NHDF-neo	bronchial:	n/a
45	chr18:24765154-24765204	NT2-D1	testis:	n/a
46	chr18:24765485-24765535	AG09309	skin:	n/a
47	chr18:24762316-24762366	SK-N-SH_RA	brain:	n/a
48	chr18:24765473-24765523	NHBE	bronchial:	n/a
49	chr18:24765643-24765693	AG09319	gingival:	n/a
50	chr18:24765485-24765535	GM06990	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:24754408..24756988-chr18:24763307..24765193,2	K562	blood:
2	chr18:24744878..24747343-chr18:24750374..24752456,2	K562	blood:
3	chr18:24770863..24773354-chr18:24775315..24777406,2	K562	blood:
4	chr18:24744878..24747343-chr18:24750374..24752456,2	K562	blood:
5	chr18:24734168..24736128-chr18:24762446..24765149,2	K562	blood:
6	chr18:24734168..24736128-chr18:24762446..24765149,2	K562	blood:
7	chr18:24770863..24773354-chr18:24775315..24777406,2	K562	blood:
8	chr18:24587162..24589841-chr18:24735427..24737669,2	K562	blood:
9	chr18:24754408..24756988-chr18:24763307..24765193,2	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-TAF4B-4	chr18:24768707-24770662	ENSG00000260372.2

No data

Variant related genes	Relation type
CHST9	TF binding region
CHST9	CpG island

Extended variants
information (count: 1931 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1931 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28693844	chr18:24722839-24722840	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147751559	chr18:24722842-24722843	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs546096868	chr18:24722856-24722857	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs564505670	chr18:24722857-24722858	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs139952906	chr18:24722899-24722900	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs550168881	chr18:24722901-24722902	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs371330002	chr18:24722906-24722907	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs529361448	chr18:24722912-24722913	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs192372924	chr18:24722930-24722931	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs8087815	chr18:24722932-24722933	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs145810763	chr18:24722938-24722939	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs558046269	chr18:24722943-24722944	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs569986882	chr18:24723030-24723031	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs537452130	chr18:24723036-24723037	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs182409362	chr18:24723038-24723039	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs565881446	chr18:24723133-24723134	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs148964989	chr18:24723137-24723138	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs375772564	chr18:24723141-24723142	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs116048001	chr18:24723157-24723158	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs551492983	chr18:24723189-24723190	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs553959263	chr18:24723218-24723219	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs72884376	chr18:24723236-24723237	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs545984839	chr18:24723277-24723278	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs145681312	chr18:24723309-24723310	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs28430781	chr18:24723321-24723322	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs146554976	chr18:24723333-24723334	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs567820243	chr18:24723348-24723349	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs561936222	chr18:24723436-24723437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529419829	chr18:24723446-24723447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111332512	chr18:24723464-24723465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547560222	chr18:24723498-24723499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs141240364	chr18:24723556-24723557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs199557832	chr18:24723558-24723559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116504646	chr18:24723561-24723562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs34245519	chr18:24723566-24723567	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs570024376	chr18:24723567-24723568	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs369037000	chr18:24723573-24723574	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs537339784	chr18:24723597-24723598	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs549795345	chr18:24723672-24723673	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs567941127	chr18:24723721-24723722	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs9947754	chr18:24723763-24723764	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs553600301	chr18:24723798-24723799	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs572141133	chr18:24723806-24723807	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs539643757	chr18:24723829-24723830	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs557977664	chr18:24723856-24723857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567914082	chr18:24723882-24723883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576454757	chr18:24723889-24723890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543720467	chr18:24723905-24723906	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs562149299	chr18:24723956-24723957	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs573968344	chr18:24723974-24723975	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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

Chromatin state (count:411 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24716400-24727400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr18:24716600-24723600	Weak transcription	Gastric	stomach
3	chr18:24716600-24724000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr18:24716600-24730200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr18:24718200-24723600	Weak transcription	Pancreas	Pancrea
6	chr18:24718400-24723600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr18:24718400-24723600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr18:24718400-24727400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr18:24718600-24723600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr18:24718800-24723200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr18:24719000-24723400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr18:24719800-24723400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr18:24721800-24723000	Active TSS	Fetal Intestine Large	intestine
14	chr18:24722000-24723200	Active TSS	Fetal Intestine Small	intestine
15	chr18:24722400-24726000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr18:24722600-24723200	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr18:24722800-24723400	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr18:24722800-24723400	Enhancers	Liver	Liver
19	chr18:24722800-24723400	Flanking Active TSS	HepG2	liver
20	chr18:24722800-24723600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr18:24723000-24723600	Weak transcription	Fetal Intestine Large	intestine
22	chr18:24723200-24723400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr18:24723200-24725600	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr18:24723200-24726200	Weak transcription	Fetal Intestine Small	intestine
25	chr18:24723400-24723600	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr18:24723400-24723600	Enhancers	HepG2	liver
27	chr18:24723400-24723800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr18:24723400-24723800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr18:24723400-24723800	Weak transcription	Liver	Liver
30	chr18:24723400-24724200	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr18:24723600-24723800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr18:24723600-24723800	Flanking Active TSS	HepG2	liver
33	chr18:24723600-24724000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr18:24723600-24724200	Enhancers	H9 Cell Line	embryonic stem cell
35	chr18:24723600-24724200	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr18:24723600-24724200	Enhancers	Fetal Intestine Large	intestine
37	chr18:24723600-24724200	Enhancers	Gastric	stomach
38	chr18:24723600-24724200	Enhancers	Psoas Muscle	Psoas
39	chr18:24723600-24724400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr18:24723600-24724600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr18:24723600-24724600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr18:24723600-24724600	Enhancers	Pancreas	Pancrea
43	chr18:24723800-24724000	Enhancers	HepG2	liver
44	chr18:24723800-24724200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr18:24723800-24724400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr18:24723800-24724600	Enhancers	Liver	Liver
47	chr18:24723800-24724600	Enhancers	Ovary	ovary
48	chr18:24723800-24726200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr18:24724000-24724200	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr18:24724000-24724200	Flanking Active TSS	HepG2	liver

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