Variant report

Variant	nsv1058214
Chromosome Location	chr18:28974612-29053891
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	chr18:29003292-29003573	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:28976731-28977863	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:28979641-28979993	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	chr18:28980698-28982615	HepG2	liver:	n/a	chr18:28980825-28980841
7	ATF1	chr18:29043383-29043412	K562	blood:	n/a	n/a
8	ATF2	chr18:29018383-29018706	GM12878	blood:	n/a	n/a
9	ATF2	chr18:29018291-29018807	GM12878	blood:	n/a	n/a
10	ATF2	chr18:28987581-28988048	GM12878	blood:	n/a	n/a
11	BACH1	chr18:28982605-28982714	K562	blood:	n/a	n/a
12	BATF	chr18:29018346-29018766	GM12878	blood:	n/a	n/a
13	BATF	chr18:28987665-28987980	GM12878	blood:	n/a	chr18:28987834-28987845
14	BATF	chr18:29018420-29018737	GM12878	blood:	n/a	n/a
15	BATF	chr18:28989277-28989486	GM12878	blood:	n/a	n/a
16	BCL11A	chr18:29018405-29018782	GM12878	blood:	n/a	n/a
17	BCL3	chr18:29018340-29018768	GM12878	blood:	n/a	n/a
18	BCL3	chr18:28987645-28987967	GM12878	blood:	n/a	n/a
19	BCLAF1	chr18:29004430-29004706	GM12878	blood:	n/a	n/a
20	BHLHE40	chr18:29004475-29004621	K562	blood:	n/a	n/a
21	BHLHE40	chr18:28981449-28982362	HepG2	liver:	n/a	n/a
22	BHLHE40	chr18:28990641-28990701	K562	blood:	n/a	n/a
23	BHLHE40	chr18:28979771-28979805	K562	blood:	n/a	n/a
24	BHLHE40	chr18:29004392-29004670	HepG2	liver:	n/a	n/a
25	BHLHE40	chr18:29004365-29004713	GM12878	blood:	n/a	n/a
26	BHLHE40	chr18:29003291-29003573	HepG2	liver:	n/a	n/a
27	CBX3	chr18:28979137-28980554	HCT-116	colon:	n/a	n/a
28	CBX3	chr18:29034067-29034484	HCT-116	colon:	n/a	n/a
29	CBX3	chr18:29033979-29034622	HCT-116	colon:	n/a	n/a
30	CCNT2	chr18:28999563-28999620	K562	blood:	n/a	n/a
31	CEBPB	chr18:29026954-29028137	K562	blood:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027139-29027150 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027139-29027150 chr18:29027957-29027970
32	CEBPB	chr18:28981969-28982182	A549	lung:	n/a	n/a
33	CEBPB	chr18:29019854-29020182	A549	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
34	CEBPB	chr18:29019855-29020147	K562	blood:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
35	CEBPB	chr18:29034088-29034345	A549	lung:	n/a	n/a
36	CEBPB	chr18:29027821-29028120	IMR90	lung:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027957-29027970
37	CEBPB	chr18:28974940-28975186	A549	lung:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
38	CEBPB	chr18:28975048-28975251	H1-hESC	embryonic stem cell:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
39	CEBPB	chr18:28974953-28975247	IMR90	lung:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
40	CEBPB	chr18:29034023-29034597	HCT-116	colon:	n/a	chr18:29034579-29034590
41	CEBPB	chr18:28979724-28979929	HepG2	liver:	n/a	n/a
42	CEBPB	chr18:28979290-28980148	HCT-116	colon:	n/a	n/a
43	CEBPB	chr18:29019860-29020209	IMR90	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
44	CEBPB	chr18:29049774-29049964	HepG2	liver:	n/a	chr18:29049873-29049884
45	CEBPB	chr18:28974932-28975260	HepG2	liver:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
46	CEBPB	chr18:29025928-29026244	K562	blood:	n/a	n/a
47	CEBPB	chr18:29019853-29020186	HepG2	liver:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
48	CEBPB	chr18:29027850-29028050	Hela-S3	cervix:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027957-29027970
49	CEBPB	chr18:29027491-29028085	H1-hESC	embryonic stem cell:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027957-29027970
50	CEBPB	chr18:28981474-28982350	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29027658-29027708	HMEC	breast:	n/a
2	chr18:29026301-29026351	T-47D	breast:	n/a
3	chr18:29026303-29026353	K562	blood:	n/a
4	chr18:29027701-29027751	HL-60	blood:	n/a
5	chr18:29027745-29027795	PrEC	prostate:	n/a
6	chr18:29027701-29027751	GM19239	blood:	n/a
7	chr18:29027745-29027795	HUVEC	blood vessel:	n/a
8	chr18:29027658-29027708	HAEpiC	amniotic membrane:	n/a
9	chr18:29026301-29026351	RPTEC	kidney:	n/a
10	chr18:29027745-29027795	Caco-2	colon:	n/a
11	chr18:29027658-29027708	GM06990	blood:	n/a
12	chr18:29027658-29027708	HPAEpiC	pulmonary alveolar:	n/a
13	chr18:29026303-29026353	SAEC	small airway:	n/a
14	chr18:29026303-29026353	HNPCEpiC	eye:	n/a
15	chr18:29026301-29026351	Hepatocyte	liver:	n/a
16	chr18:29027701-29027751	HCF	heart:	n/a
17	chr18:29027701-29027751	T-47D	breast:	n/a
18	chr18:29027885-29027935	HepG2	liver:	n/a
19	chr18:29026301-29026351	HL-60	blood:	n/a
20	chr18:29026303-29026353	HRE	kidney:	n/a
21	chr18:29026303-29026353	AoSMC	blood vessel:	n/a
22	chr18:29026301-29026351	AG04450	lung:	fetal
23	chr18:29027745-29027795	NHBE	bronchial:	n/a
24	chr18:29027885-29027935	NHBE	bronchial:	n/a
25	chr18:29027658-29027708	ECC-1	luminal epithelium:	n/a
26	chr18:29026303-29026353	AG04449	skin:	fetal
27	chr18:29026303-29026353	HMEC	breast:	n/a
28	chr18:29027745-29027795	GM12878	blood:	n/a
29	chr18:29027658-29027708	AG09319	gingival:	n/a
30	chr18:29026301-29026351	CMK	blood:	n/a
31	chr18:29026301-29026351	HEEpiC	esophagus:	n/a
32	chr18:29027885-29027935	HEK293	kidney:	embryo
33	chr18:29027745-29027795	AG04450	lung:	fetal
34	chr18:29027745-29027795	SK-N-MC	brain:	n/a
35	chr18:29027658-29027708	HCT-116	colon:	n/a
36	chr18:29027885-29027935	HNPCEpiC	eye:	n/a
37	chr18:29026303-29026353	BJ	skin:	n/a
38	chr18:29026301-29026351	ECC-1	luminal epithelium:	n/a
39	chr18:29027658-29027708	HUVEC	blood vessel:	n/a
40	chr18:29027701-29027751	A549	lung:	n/a
41	chr18:29027745-29027795	SK-N-SH	brain:	n/a
42	chr18:29027701-29027751	NH-A	brain:	n/a
43	chr18:29027745-29027795	IMR90	lung:	fetal
44	chr18:29026303-29026353	U87	brain:	n/a
45	chr18:29026303-29026353	PFSK-1	brain:	n/a
46	chr18:29027745-29027795	GM12892	blood:	n/a
47	chr18:29027745-29027795	GM06990	blood:	n/a
48	chr18:29026301-29026351	MCF10A-Er-Src	breast:	n/a
49	chr18:29026301-29026351	AG10803	skin:	n/a
50	chr18:29027701-29027751	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:29038496..29040369-chr18:29042094..29044336,2	K562	blood:
2	chr18:29044429..29046768-chr18:29048309..29050870,3	K562	blood:
3	chr18:29003994..29005325-chr18:29086073..29087125,6	MCF-7	breast:
4	chr18:29001628..29005715-chr18:29006148..29009419,4	K562	blood:
5	chr18:29002388..29006763-chr18:29077410..29081754,4	K562	blood:
6	chr18:29004133..29005005-chr18:29399717..29400321,2	K562	blood:
7	chr18:29038234..29040822-chr18:29041279..29043976,2	MCF-7	breast:
8	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
9	chr18:29004062..29004974-chr18:29135505..29136292,3	MCF-7	breast:
10	chr18:29003931..29004668-chr18:29134416..29135171,2	MCF-7	breast:
11	chr18:29004154..29005000-chr18:29143490..29144004,2	K562	blood:
12	chr18:29003997..29005002-chr18:29143774..29144455,3	MCF-7	breast:
13	chr18:28821484..28823254-chr18:29002472..29004133,2	K562	blood:
14	chr18:29046909..29049478-chr18:29076853..29079838,2	K562	blood:
15	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
16	chr18:29003549..29006106-chr18:29084281..29086820,2	MCF-7	breast:
17	chr18:29038234..29040822-chr18:29041279..29043976,2	MCF-7	breast:
18	chr18:28971505..28973722-chr18:28976105..28978957,2	K562	blood:
19	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
20	chr18:29044429..29046768-chr18:29048309..29050870,3	K562	blood:
21	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
22	chr18:28980664..28983039-chr18:28984918..28986737,2	MCF-7	breast:
23	chr18:28786778..28788708-chr18:29017378..29018896,2	MCF-7	breast:
24	chr18:29042545..29045965-chr18:29077171..29079744,3	K562	blood:
25	chr18:29038496..29040369-chr18:29042094..29044336,2	K562	blood:

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

Variant related genes	Relation type
ENSG00000266729	TF binding region
DSG3	TF binding region
ENSG00000266729	CpG island
DSG3	CpG island
ENSG00000046604	chromatin interactions
ENSG00000266521	chromatin interactions
ENSG00000266729	chromatin interactions

Extended variants
information (count: 3298 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3298 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5823804	chr18:28974644-28974645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541026570	chr18:28974645-28974646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76405893	chr18:28974658-28974659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs62095163	chr18:28974660-28974661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144448853	chr18:28974680-28974681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs151083673	chr18:28974711-28974712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565644132	chr18:28974745-28974746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536594946	chr18:28974752-28974753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555654755	chr18:28974767-28974768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187350564	chr18:28974772-28974773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534847927	chr18:28974777-28974778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553201799	chr18:28974849-28974850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140024060	chr18:28974873-28974874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs193260067	chr18:28974889-28974890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553588516	chr18:28974921-28974922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557919677	chr18:28974935-28974936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185506579	chr18:28974969-28974970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188050437	chr18:28974991-28974992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149842858	chr18:28975051-28975052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs543419524	chr18:28975074-28975075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9304095	chr18:28975132-28975133	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs529524680	chr18:28975137-28975138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201353732	chr18:28975144-28975145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541271520	chr18:28975159-28975160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145472808	chr18:28975165-28975166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192231910	chr18:28975196-28975197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543026869	chr18:28975235-28975236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371425847	chr18:28975258-28975259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1290322	chr18:28975279-28975280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185017378	chr18:28975284-28975285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569621715	chr18:28975478-28975479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs141075806	chr18:28975481-28975482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548684923	chr18:28975501-28975502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34399613	chr18:28975524-28975525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376571256	chr18:28975527-28975528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375789621	chr18:28975552-28975553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs118115028	chr18:28975589-28975590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552968569	chr18:28975590-28975591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs572506346	chr18:28975657-28975658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534907027	chr18:28975681-28975682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145144187	chr18:28975708-28975709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546208642	chr18:28975728-28975729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571471240	chr18:28975775-28975776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538428134	chr18:28975779-28975780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147600056	chr18:28975790-28975791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576445865	chr18:28975801-28975802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142062862	chr18:28975802-28975803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574032320	chr18:28975819-28975820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541333259	chr18:28975828-28975829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188601477	chr18:28975852-28975853	Weak transcription Enhancers	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:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28972000-28976400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr18:28972800-28976800	Weak transcription	Fetal Kidney	kidney
3	chr18:28973400-28976600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr18:28973600-28975600	Weak transcription	Duodenum Mucosa	Duodenum
5	chr18:28973600-28989400	Weak transcription	Esophagus	oesophagus
6	chr18:28974200-28975400	Weak transcription	HepG2	liver
7	chr18:28975000-28983400	Enhancers	Fetal Intestine Large	intestine
8	chr18:28975400-28975600	Enhancers	Fetal Intestine Small	intestine
9	chr18:28975400-28977000	Enhancers	HepG2	liver
10	chr18:28975600-28975800	Enhancers	Duodenum Mucosa	Duodenum
11	chr18:28975600-28975800	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr18:28975600-28976200	Weak transcription	Fetal Intestine Small	intestine
13	chr18:28975800-28976400	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr18:28975800-28976600	Weak transcription	Duodenum Mucosa	Duodenum
15	chr18:28975800-28976600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr18:28976200-28983600	Enhancers	Fetal Intestine Small	intestine
17	chr18:28976400-28976600	Enhancers	Rectal Mucosa Donor 29	rectum
18	chr18:28976400-28976800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr18:28976400-28977000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
20	chr18:28976400-28977800	Enhancers	Left Ventricle	heart
21	chr18:28976600-28976800	Active TSS	Adipose Nuclei	Adipose
22	chr18:28976600-28977000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr18:28976600-28977000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
24	chr18:28976600-28977400	Enhancers	Right Atrium	heart
25	chr18:28976600-28977600	Enhancers	Liver	Liver
26	chr18:28976600-28977600	Enhancers	Duodenum Mucosa	Duodenum
27	chr18:28976600-28977600	Enhancers	Stomach Mucosa	stomach
28	chr18:28976600-28978400	Enhancers	Small Intestine	intestine
29	chr18:28976600-28979400	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr18:28976800-28977000	Flanking Active TSS	Adipose Nuclei	Adipose
31	chr18:28976800-28977000	Enhancers	Colon Smooth Muscle	Colon
32	chr18:28976800-28977400	Enhancers	Fetal Kidney	kidney
33	chr18:28976800-28977400	Enhancers	Gastric	stomach
34	chr18:28976800-28977600	Enhancers	Fetal Stomach	stomach
35	chr18:28976800-28977600	Enhancers	Hela-S3	cervix
36	chr18:28976800-28977800	Enhancers	Fetal Heart	heart
37	chr18:28976800-28977800	Enhancers	Fetal Lung	lung
38	chr18:28976800-28978000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr18:28976800-28980200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr18:28977000-28977200	Active TSS	Adipose Nuclei	Adipose
41	chr18:28977000-28977400	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr18:28977000-28977400	Flanking Active TSS	HepG2	liver
43	chr18:28977000-28979400	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr18:28977200-28977400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr18:28977200-28977600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr18:28977200-28977600	Flanking Active TSS	Adipose Nuclei	Adipose
47	chr18:28977200-28977800	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr18:28977200-28977800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr18:28977200-28977800	Enhancers	A549	lung
50	chr18:28977200-28979200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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