Variant report

Variant	nsv576633
Chromosome Location	chr18:28972363-29038123
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	chr18:28980698-28982615	HepG2	liver:	n/a	chr18:28980825-28980841
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	chr18:29018291-29018807	GM12878	blood:	n/a	n/a
8	ATF2	chr18:28987581-28988048	GM12878	blood:	n/a	n/a
9	ATF2	chr18:29018383-29018706	GM12878	blood:	n/a	n/a
10	BACH1	chr18:28982605-28982714	K562	blood:	n/a	n/a
11	BATF	chr18:29018420-29018737	GM12878	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	chr18:28989277-28989486	GM12878	blood:	n/a	n/a
15	BCL11A	chr18:29018405-29018782	GM12878	blood:	n/a	n/a
16	BCL3	chr18:28987645-28987967	GM12878	blood:	n/a	n/a
17	BCL3	chr18:29018340-29018768	GM12878	blood:	n/a	n/a
18	BCLAF1	chr18:29004430-29004706	GM12878	blood:	n/a	n/a
19	BHLHE40	chr18:29004392-29004670	HepG2	liver:	n/a	n/a
20	BHLHE40	chr18:29003291-29003573	HepG2	liver:	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	chr18:29004365-29004713	GM12878	blood:	n/a	n/a
24	BHLHE40	chr18:29004475-29004621	K562	blood:	n/a	n/a
25	BHLHE40	chr18:28979771-28979805	K562	blood:	n/a	n/a
26	CBX3	chr18:29033979-29034622	HCT-116	colon:	n/a	n/a
27	CBX3	chr18:29034067-29034484	HCT-116	colon:	n/a	n/a
28	CBX3	chr18:28979137-28980554	HCT-116	colon:	n/a	n/a
29	CCNT2	chr18:28999563-28999620	K562	blood:	n/a	n/a
30	CEBPB	chr18:28979724-28979929	HepG2	liver:	n/a	n/a
31	CEBPB	chr18:28974947-28975271	K562	blood:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
32	CEBPB	chr18:28981474-28982350	HepG2	liver:	n/a	n/a
33	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
34	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
35	CEBPB	chr18:28974932-28975260	HepG2	liver:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
36	CEBPB	chr18:29019853-29020186	HepG2	liver:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
37	CEBPB	chr18:29034023-29034597	HCT-116	colon:	n/a	chr18:29034579-29034590
38	CEBPB	chr18:28972607-28972963	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr18:28981969-28982182	A549	lung:	n/a	n/a
40	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
41	CEBPB	chr18:29027614-29028137	HepG2	liver:	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
42	CEBPB	chr18:29027824-29028093	A549	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
43	CEBPB	chr18:28974953-28975247	IMR90	lung:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
44	CEBPB	chr18:28979290-28980148	HCT-116	colon:	n/a	n/a
45	CEBPB	chr18:29019860-29020209	IMR90	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
46	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
47	CEBPB	chr18:29025928-29026244	K562	blood:	n/a	n/a
48	CEBPB	chr18:28975048-28975251	H1-hESC	embryonic stem cell:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
49	CEBPB	chr18:28979105-28980269	HCT-116	colon:	n/a	n/a
50	CEBPB	chr18:29034088-29034345	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29027658-29027708	SK-N-MC	brain:	n/a
2	chr18:29027658-29027708	SK-N-MC	brain:	n/a
3	chr18:29026303-29026353	ProgFib	skin:	n/a
4	chr18:29027658-29027708	IMR90	lung:	fetal
5	chr18:29027701-29027751	SK-N-SH	brain:	n/a
6	chr18:29027701-29027751	ProgFib	skin:	n/a
7	chr18:29027885-29027935	GM12891	blood:	n/a
8	chr18:29026301-29026351	NT2-D1	testis:	n/a
9	chr18:29026303-29026353	ECC-1	luminal epithelium:	n/a
10	chr18:29027658-29027708	NHDF-neo	bronchial:	n/a
11	chr18:29026301-29026351	GM06990	blood:	n/a
12	chr18:29026301-29026351	ECC-1	luminal epithelium:	n/a
13	chr18:29026301-29026351	BE2_C	brain:	n/a
14	chr18:29027701-29027751	SKMC	muscle:	n/a
15	chr18:29027701-29027751	GM12878	blood:	n/a
16	chr18:29026303-29026353	PFSK-1	brain:	n/a
17	chr18:29027745-29027795	SAEC	small airway:	n/a
18	chr18:29027658-29027708	ECC-1	luminal epithelium:	n/a
19	chr18:29026301-29026351	HRPEpiC	eye:	n/a
20	chr18:29026301-29026351	AG04449	skin:	fetal
21	chr18:29027701-29027751	BJ	skin:	n/a
22	chr18:29027745-29027795	MCF-7	breast:	n/a
23	chr18:29027701-29027751	NT2-D1	testis:	n/a
24	chr18:29027885-29027935	T-47D	breast:	n/a
25	chr18:29026303-29026353	GM12891	blood:	n/a
26	chr18:29027885-29027935	SAEC	small airway:	n/a
27	chr18:29027745-29027795	Jurkat	blood:	n/a
28	chr18:29027885-29027935	HCPEpiC	choroid plexus:	n/a
29	chr18:29027701-29027751	RPTEC	kidney:	n/a
30	chr18:29027885-29027935	Hela-S3	cervix:	n/a
31	chr18:29027745-29027795	RPTEC	kidney:	n/a
32	chr18:29027885-29027935	HepG2	liver:	n/a
33	chr18:29027701-29027751	NHBE	bronchial:	n/a
34	chr18:29027701-29027751	T-47D	breast:	n/a
35	chr18:29026301-29026351	AG04450	lung:	fetal
36	chr18:29027885-29027935	H1-hESC	embryonic stem cell:	embryo
37	chr18:29027701-29027751	Hela-S3	cervix:	n/a
38	chr18:29027745-29027795	ProgFib	skin:	n/a
39	chr18:29027745-29027795	LNCaP	prostate:	n/a
40	chr18:29027658-29027708	LNCaP	prostate:	n/a
41	chr18:29026301-29026351	HAEpiC	amniotic membrane:	n/a
42	chr18:29027745-29027795	NB4	blood:	n/a
43	chr18:29027658-29027708	HIPEpiC	eye:	n/a
44	chr18:29027745-29027795	SK-N-SH_RA	brain:	n/a
45	chr18:29027885-29027935	RPTEC	kidney:	n/a
46	chr18:29027745-29027795	GM12878	blood:	n/a
47	chr18:29027658-29027708	BJ	skin:	n/a
48	chr18:29026303-29026353	AG04449	skin:	fetal
49	chr18:29027885-29027935	NHDF-neo	bronchial:	n/a
50	chr18:29027745-29027795	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:29003549..29006106-chr18:29084281..29086820,2	MCF-7	breast:
2	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
3	chr18:28821484..28823254-chr18:29002472..29004133,2	K562	blood:
4	chr18:28980664..28983039-chr18:28984918..28986737,2	MCF-7	breast:
5	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
6	chr18:28971505..28973722-chr18:28976105..28978957,2	K562	blood:
7	chr18:28786778..28788708-chr18:29017378..29018896,2	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	chr18:29004133..29005005-chr18:29399717..29400321,2	K562	blood:
11	chr18:29003931..29004668-chr18:29134416..29135171,2	MCF-7	breast:
12	chr18:29004154..29005000-chr18:29143490..29144004,2	K562	blood:
13	chr18:28971505..28973722-chr18:28976105..28978957,2	K562	blood:
14	chr18:29003997..29005002-chr18:29143774..29144455,3	MCF-7	breast:
15	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
16	chr18:29001628..29005715-chr18:29006148..29009419,4	K562	blood:
17	chr18:29003994..29005325-chr18:29086073..29087125,6	MCF-7	breast:
18	chr18:29002388..29006763-chr18:29077410..29081754,4	K562	blood:

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

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

Extended variants
information (count: 2691 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2691 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17802140	chr18:28972363-28972364	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140213167	chr18:28972382-28972383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534492418	chr18:28972391-28972392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79871893	chr18:28972433-28972434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571065019	chr18:28972434-28972435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146950019	chr18:28972439-28972440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138117710	chr18:28972587-28972588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143589940	chr18:28972614-28972615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145938207	chr18:28972687-28972688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553350147	chr18:28972703-28972704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553579352	chr18:28972774-28972775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73953136	chr18:28972781-28972782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545703125	chr18:28972822-28972823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563994398	chr18:28972826-28972827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs80098010	chr18:28972837-28972838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543571772	chr18:28972919-28972920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562873488	chr18:28972923-28972924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138674522	chr18:28972938-28972939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548646582	chr18:28972942-28972943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566860945	chr18:28972948-28972949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527643427	chr18:28973055-28973056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs202242359	chr18:28973115-28973116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148982015	chr18:28973116-28973117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs59850259	chr18:28973121-28973122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189045904	chr18:28973185-28973186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571096299	chr18:28973198-28973199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560503518	chr18:28973213-28973214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538070805	chr18:28973260-28973261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527809154	chr18:28973270-28973271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546345940	chr18:28973277-28973278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568109924	chr18:28973279-28973280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535526813	chr18:28973313-28973314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553413225	chr18:28973340-28973341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181482692	chr18:28973370-28973371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571712487	chr18:28973421-28973422	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs372774216	chr18:28973428-28973429	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs557648930	chr18:28973429-28973430	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs185724359	chr18:28973461-28973462	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs376016375	chr18:28973537-28973538	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs543278102	chr18:28973582-28973583	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs190984608	chr18:28973595-28973596	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs181930163	chr18:28973620-28973621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542350433	chr18:28973688-28973689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560522666	chr18:28973697-28973698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530858143	chr18:28973704-28973705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527707152	chr18:28973705-28973706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149319433	chr18:28973706-28973707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79394396	chr18:28973726-28973727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186124854	chr18:28973747-28973748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34195171	chr18:28973759-28973760	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:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28960600-28973400	Weak transcription	Esophagus	oesophagus
2	chr18:28968400-28973400	Weak transcription	HepG2	liver
3	chr18:28972000-28976400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr18:28972400-28972800	Enhancers	Fetal Kidney	kidney
5	chr18:28972800-28976800	Weak transcription	Fetal Kidney	kidney
6	chr18:28973400-28973600	Enhancers	Duodenum Mucosa	Duodenum
7	chr18:28973400-28973600	ZNF genes & repeats	Esophagus	oesophagus
8	chr18:28973400-28973600	Enhancers	Small Intestine	intestine
9	chr18:28973400-28973600	Enhancers	HepG2	liver
10	chr18:28973400-28976600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr18:28973600-28974000	Weak transcription	HepG2	liver
12	chr18:28973600-28975600	Weak transcription	Duodenum Mucosa	Duodenum
13	chr18:28973600-28989400	Weak transcription	Esophagus	oesophagus
14	chr18:28974000-28974200	Enhancers	HepG2	liver
15	chr18:28974200-28975400	Weak transcription	HepG2	liver
16	chr18:28975000-28983400	Enhancers	Fetal Intestine Large	intestine
17	chr18:28975400-28975600	Enhancers	Fetal Intestine Small	intestine
18	chr18:28975400-28977000	Enhancers	HepG2	liver
19	chr18:28975600-28975800	Enhancers	Duodenum Mucosa	Duodenum
20	chr18:28975600-28975800	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr18:28975600-28976200	Weak transcription	Fetal Intestine Small	intestine
22	chr18:28975800-28976400	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr18:28975800-28976600	Weak transcription	Duodenum Mucosa	Duodenum
24	chr18:28975800-28976600	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr18:28976200-28983600	Enhancers	Fetal Intestine Small	intestine
26	chr18:28976400-28976600	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr18:28976400-28976800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr18:28976400-28977000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
29	chr18:28976400-28977800	Enhancers	Left Ventricle	heart
30	chr18:28976600-28976800	Active TSS	Adipose Nuclei	Adipose
31	chr18:28976600-28977000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr18:28976600-28977000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
33	chr18:28976600-28977400	Enhancers	Right Atrium	heart
34	chr18:28976600-28977600	Enhancers	Liver	Liver
35	chr18:28976600-28977600	Enhancers	Duodenum Mucosa	Duodenum
36	chr18:28976600-28977600	Enhancers	Stomach Mucosa	stomach
37	chr18:28976600-28978400	Enhancers	Small Intestine	intestine
38	chr18:28976600-28979400	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr18:28976800-28977000	Flanking Active TSS	Adipose Nuclei	Adipose
40	chr18:28976800-28977000	Enhancers	Colon Smooth Muscle	Colon
41	chr18:28976800-28977400	Enhancers	Fetal Kidney	kidney
42	chr18:28976800-28977400	Enhancers	Gastric	stomach
43	chr18:28976800-28977600	Enhancers	Fetal Stomach	stomach
44	chr18:28976800-28977600	Enhancers	Hela-S3	cervix
45	chr18:28976800-28977800	Enhancers	Fetal Heart	heart
46	chr18:28976800-28977800	Enhancers	Fetal Lung	lung
47	chr18:28976800-28978000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr18:28976800-28980200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr18:28977000-28977200	Active TSS	Adipose Nuclei	Adipose
50	chr18:28977000-28977400	Active TSS	Rectal Mucosa Donor 29	rectum

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