Variant report

Variant	nsv909517
Chromosome Location	chr18:28956904-29018114
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:642)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:642 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:28980698-28982615	HepG2	liver:	n/a	chr18:28980825-28980841
2	ARID3A	chr18:29003292-29003573	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:28976731-28977863	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:29004374-29004617	K562	blood:	n/a	n/a
5	ARID3A	chr18:29016896-29016955	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:28979641-28979993	HepG2	liver:	n/a	n/a
7	ATF2	chr18:28987581-28988048	GM12878	blood:	n/a	n/a
8	BACH1	chr18:28982605-28982714	K562	blood:	n/a	n/a
9	BATF	chr18:28987665-28987980	GM12878	blood:	n/a	chr18:28987834-28987845
10	BATF	chr18:28989277-28989486	GM12878	blood:	n/a	n/a
11	BCL3	chr18:28987645-28987967	GM12878	blood:	n/a	n/a
12	BCLAF1	chr18:29004430-29004706	GM12878	blood:	n/a	n/a
13	BHLHE40	chr18:28990641-28990701	K562	blood:	n/a	n/a
14	BHLHE40	chr18:29003291-29003573	HepG2	liver:	n/a	n/a
15	BHLHE40	chr18:28979771-28979805	K562	blood:	n/a	n/a
16	BHLHE40	chr18:29004392-29004670	HepG2	liver:	n/a	n/a
17	BHLHE40	chr18:29004365-29004713	GM12878	blood:	n/a	n/a
18	BHLHE40	chr18:28981449-28982362	HepG2	liver:	n/a	n/a
19	BHLHE40	chr18:29004475-29004621	K562	blood:	n/a	n/a
20	CBX3	chr18:28979137-28980554	HCT-116	colon:	n/a	n/a
21	CCNT2	chr18:28999563-28999620	K562	blood:	n/a	n/a
22	CEBPB	chr18:28974940-28975186	A549	lung:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
23	CEBPB	chr18:28979290-28980148	HCT-116	colon:	n/a	n/a
24	CEBPB	chr18:28963692-28963883	HepG2	liver:	n/a	chr18:28963735-28963746
25	CEBPB	chr18:28974932-28975260	HepG2	liver:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
26	CEBPB	chr18:28972607-28972963	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr18:28981969-28982182	A549	lung:	n/a	n/a
28	CEBPB	chr18:28975048-28975251	H1-hESC	embryonic stem cell:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
29	CEBPB	chr18:28979105-28980269	HCT-116	colon:	n/a	n/a
30	CEBPB	chr18:28974953-28975247	IMR90	lung:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
31	CEBPB	chr18:28966630-28966940	K562	blood:	n/a	chr18:28966789-28966800
32	CEBPB	chr18:28966671-28966959	HepG2	liver:	n/a	chr18:28966789-28966800
33	CEBPB	chr18:28966625-28966965	ECC-1	luminal epithelium:	n/a	chr18:28966789-28966800
34	CEBPB	chr18:28981474-28982350	HepG2	liver:	n/a	n/a
35	CEBPB	chr18:28974947-28975271	K562	blood:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
36	CEBPB	chr18:28979724-28979929	HepG2	liver:	n/a	n/a
37	CHD2	chr18:28976571-28976605	HepG2	liver:	n/a	n/a
38	CHD2	chr18:28977252-28977482	HepG2	liver:	n/a	n/a
39	CTCF	chr18:29004426-29004699	A549	lung:	n/a	n/a
40	CTCF	chr18:29004480-29004630	HMF	breast:	n/a	n/a
41	CTCF	chr18:29004500-29004650	GM12872	blood:	n/a	n/a
42	CTCF	chr18:29017020-29017170	HepG2	liver:	n/a	n/a
43	CTCF	chr18:29004480-29004630	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr18:29004480-29004630	GM12869	blood:	n/a	n/a
45	CTCF	chr18:29003999-29004968	A549	lung:	n/a	n/a
46	CTCF	chr18:28999487-28999491	NHEK	skin:	n/a	n/a
47	CTCF	chr18:29016957-29017069	GM12878	blood:	n/a	n/a
48	CTCF	chr18:29004412-29004668	HepG2	liver:	n/a	n/a
49	CTCF	chr18:29004440-29004590	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr18:29004480-29004630	GM12872	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:28957111-28957161	HRPEpiC	eye:	n/a
2	chr18:28957111-28957161	NT2-D1	testis:	n/a
3	chr18:28957111-28957161	GM12892	blood:	n/a
4	chr18:28957111-28957161	NH-A	brain:	n/a
5	chr18:28957111-28957161	SK-N-MC	brain:	n/a
6	chr18:28957111-28957161	NHBE	bronchial:	n/a
7	chr18:28957111-28957161	HEK293	kidney:	embryo
8	chr18:28957111-28957161	AG04450	lung:	fetal
9	chr18:28957111-28957161	RPTEC	kidney:	n/a
10	chr18:28957111-28957161	ovcar-3	ovarian:	n/a
11	chr18:28957111-28957161	HCF	heart:	n/a
12	chr18:28957111-28957161	ECC-1	luminal epithelium:	n/a
13	chr18:28957111-28957161	ProgFib	skin:	n/a
14	chr18:28957111-28957161	AG04449	skin:	fetal
15	chr18:28957111-28957161	HCM	heart:	n/a
16	chr18:28957111-28957161	IMR90	lung:	fetal
17	chr18:28957111-28957161	HUVEC	blood vessel:	n/a
18	chr18:28957111-28957161	HEEpiC	esophagus:	n/a
19	chr18:28957111-28957161	HCPEpiC	choroid plexus:	n/a
20	chr18:28957111-28957161	GM19239	blood:	n/a
21	chr18:28957111-28957161	GM12878	blood:	n/a
22	chr18:28957111-28957161	AG09309	skin:	n/a
23	chr18:28957111-28957161	H1-hESC	embryonic stem cell:	embryo
24	chr18:28957111-28957161	PFSK-1	brain:	n/a
25	chr18:28957111-28957161	HRE	kidney:	n/a
26	chr18:28957111-28957161	GM12891	blood:	n/a
27	chr18:28957111-28957161	HPAEpiC	pulmonary alveolar:	n/a
28	chr18:28957111-28957161	Hela-S3	cervix:	n/a
29	chr18:28957111-28957161	NHDF-neo	bronchial:	n/a
30	chr18:28957111-28957161	LNCaP	prostate:	n/a
31	chr18:28957111-28957161	PANC-1	pancreas:	n/a
32	chr18:28957111-28957161	HIPEpiC	eye:	n/a
33	chr18:28957111-28957161	AG09319	gingival:	n/a
34	chr18:28957111-28957161	AoSMC	blood vessel:	n/a
35	chr18:28957111-28957161	SAEC	small airway:	n/a
36	chr18:28957111-28957161	T-47D	breast:	n/a
37	chr18:28957111-28957161	SK-N-SH_RA	brain:	n/a
38	chr18:28957111-28957161	HL-60	blood:	n/a
39	chr18:28957111-28957161	MCF10A-Er-Src	breast:	n/a
40	chr18:28957111-28957161	HAEpiC	amniotic membrane:	n/a
41	chr18:28957111-28957161	GM06990	blood:	n/a
42	chr18:28957111-28957161	Jurkat	blood:	n/a
43	chr18:28957111-28957161	HMEC	breast:	n/a
44	chr18:28957111-28957161	HepG2	liver:	n/a
45	chr18:28957111-28957161	NB4	blood:	n/a
46	chr18:28957111-28957161	K562	blood:	n/a
47	chr18:28957111-28957161	SK-N-SH	brain:	n/a
48	chr18:28957111-28957161	HRCEpiC	kidney:	n/a
49	chr18:28957111-28957161	U87	brain:	n/a
50	chr18:28957111-28957161	PrEC	prostate:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:29001628..29005715-chr18:29006148..29009419,4	K562	blood:
2	chr18:29004062..29004974-chr18:29135505..29136292,3	MCF-7	breast:
3	chr18:29003549..29006106-chr18:29084281..29086820,2	MCF-7	breast:
4	chr18:28971505..28973722-chr18:28976105..28978957,2	K562	blood:
5	chr18:28786778..28788708-chr18:29017378..29018896,2	MCF-7	breast:
6	chr18:28821484..28823254-chr18:29002472..29004133,2	K562	blood:
7	chr18:29003994..29005325-chr18:29086073..29087125,6	MCF-7	breast:
8	chr18:28980664..28983039-chr18:28984918..28986737,2	MCF-7	breast:
9	chr18:28955738..28957988-chr18:28962797..28964940,2	K562	blood:
10	chr18:28958201..28959975-chr18:28963348..28965606,2	MCF-7	breast:
11	chr18:28958201..28959975-chr18:28963348..28965606,2	MCF-7	breast:
12	chr18:29003931..29004668-chr18:29134416..29135171,2	MCF-7	breast:
13	chr18:28971505..28973722-chr18:28976105..28978957,2	K562	blood:
14	chr18:29004154..29005000-chr18:29143490..29144004,2	K562	blood:
15	chr18:29003997..29005002-chr18:29143774..29144455,3	MCF-7	breast:
16	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
17	chr18:29004133..29005005-chr18:29399717..29400321,2	K562	blood:
18	chr18:29002388..29006763-chr18:29077410..29081754,4	K562	blood:
19	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
20	chr18:28949758..28952384-chr18:28959857..28961586,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DSC1-1	chr18:29006796-29006890	ENSG00000266729.1
2	lnc-DSC1-1	chr18:29006796-29006951	ENSG00000266729.1

No data

Variant related genes	Relation type
ENSG00000207240	TF binding region
ENSG00000266729	TF binding region
ENSG00000207240	CpG island
ENSG00000266729	CpG island
ENSG00000046604	chromatin interactions
ENSG00000175065	chromatin interactions
ENSG00000266729	chromatin interactions

Extended variants
information (count: 2548 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2548 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs36101975	chr18:28956904-28956905	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372155276	chr18:28956921-28956922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367670127	chr18:28956925-28956926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375558885	chr18:28956985-28956986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111759738	chr18:28956986-28956987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369450835	chr18:28956987-28956988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562185430	chr18:28957013-28957014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113750504	chr18:28957020-28957021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547846016	chr18:28957023-28957024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565913208	chr18:28957029-28957030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540171103	chr18:28957039-28957040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140442214	chr18:28957042-28957043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182296684	chr18:28957043-28957044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10502570	chr18:28957072-28957073	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs115738534	chr18:28957081-28957082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545199573	chr18:28957082-28957083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534395366	chr18:28957100-28957101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553997625	chr18:28957151-28957152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552981599	chr18:28957255-28957256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577558345	chr18:28957267-28957268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187372080	chr18:28957278-28957279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572154437	chr18:28957298-28957299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575467381	chr18:28957307-28957308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542859826	chr18:28957316-28957317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374591157	chr18:28957321-28957322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189278256	chr18:28957324-28957325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs180810489	chr18:28957333-28957334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73410241	chr18:28957382-28957383	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs559738022	chr18:28957389-28957390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555813091	chr18:28957397-28957398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145525050	chr18:28957402-28957403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138733660	chr18:28957523-28957524	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs111585678	chr18:28957524-28957525	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs531073859	chr18:28957553-28957554	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs549195826	chr18:28957662-28957663	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs567520502	chr18:28957679-28957680	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs575546023	chr18:28957689-28957690	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs552804833	chr18:28957695-28957696	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs73410243	chr18:28957725-28957726	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs148917171	chr18:28957749-28957750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11875880	chr18:28957811-28957812	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs575645022	chr18:28957831-28957832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371792421	chr18:28957854-28957855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185180257	chr18:28957858-28957859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73410245	chr18:28957862-28957863	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs374236482	chr18:28957885-28957886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143650325	chr18:28957898-28957899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs80092787	chr18:28957900-28957901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559593356	chr18:28957912-28957913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148125781	chr18:28957917-28957918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28956800-28961000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr18:28959400-28959800	Enhancers	Fetal Heart	heart
3	chr18:28960200-28960600	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr18:28960200-28960600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr18:28960200-28960600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr18:28960200-28960600	Enhancers	Esophagus	oesophagus
7	chr18:28960400-28961800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr18:28960400-28962000	Enhancers	NHEK	skin
9	chr18:28960600-28973400	Weak transcription	Esophagus	oesophagus
10	chr18:28960800-28961600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr18:28961000-28961600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr18:28962000-28962800	Enhancers	Fetal Intestine Large	intestine
13	chr18:28962000-28962800	Enhancers	Fetal Intestine Small	intestine
14	chr18:28966200-28968200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr18:28966800-28967000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr18:28966800-28967200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr18:28967000-28967200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr18:28967000-28968000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr18:28968000-28968400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr18:28968000-28968400	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr18:28968000-28968400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr18:28968000-28968400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr18:28968000-28968400	Enhancers	HepG2	liver
24	chr18:28968000-28968600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr18:28968400-28973400	Weak transcription	HepG2	liver
26	chr18:28972000-28976400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr18:28972400-28972800	Enhancers	Fetal Kidney	kidney
28	chr18:28972800-28976800	Weak transcription	Fetal Kidney	kidney
29	chr18:28973400-28973600	Enhancers	Duodenum Mucosa	Duodenum
30	chr18:28973400-28973600	ZNF genes & repeats	Esophagus	oesophagus
31	chr18:28973400-28973600	Enhancers	Small Intestine	intestine
32	chr18:28973400-28973600	Enhancers	HepG2	liver
33	chr18:28973400-28976600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr18:28973600-28974000	Weak transcription	HepG2	liver
35	chr18:28973600-28975600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr18:28973600-28989400	Weak transcription	Esophagus	oesophagus
37	chr18:28974000-28974200	Enhancers	HepG2	liver
38	chr18:28974200-28975400	Weak transcription	HepG2	liver
39	chr18:28975000-28983400	Enhancers	Fetal Intestine Large	intestine
40	chr18:28975400-28975600	Enhancers	Fetal Intestine Small	intestine
41	chr18:28975400-28977000	Enhancers	HepG2	liver
42	chr18:28975600-28975800	Enhancers	Duodenum Mucosa	Duodenum
43	chr18:28975600-28975800	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr18:28975600-28976200	Weak transcription	Fetal Intestine Small	intestine
45	chr18:28975800-28976400	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr18:28975800-28976600	Weak transcription	Duodenum Mucosa	Duodenum
47	chr18:28975800-28976600	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr18:28976200-28983600	Enhancers	Fetal Intestine Small	intestine
49	chr18:28976400-28976600	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr18:28976400-28976800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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