Variant report

Variant	nsv576632
Chromosome Location	chr18:28969044-29056465
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	chr18:29004374-29004617	K562	blood:	n/a	n/a
2	ARID3A	chr18:28979641-28979993	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:29003292-29003573	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:29016896-29016955	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:28980698-28982615	HepG2	liver:	n/a	chr18:28980825-28980841
6	ARID3A	chr18:28976731-28977863	HepG2	liver:	n/a	n/a
7	ATF1	chr18:29043383-29043412	K562	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	ATF2	chr18:29018291-29018807	GM12878	blood:	n/a	n/a
11	BACH1	chr18:28982605-28982714	K562	blood:	n/a	n/a
12	BATF	chr18:28987665-28987980	GM12878	blood:	n/a	chr18:28987834-28987845
13	BATF	chr18:28989277-28989486	GM12878	blood:	n/a	n/a
14	BATF	chr18:29018346-29018766	GM12878	blood:	n/a	n/a
15	BATF	chr18:29018420-29018737	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	chr18:29004365-29004713	GM12878	blood:	n/a	n/a
22	BHLHE40	chr18:28981449-28982362	HepG2	liver:	n/a	n/a
23	BHLHE40	chr18:28990641-28990701	K562	blood:	n/a	n/a
24	BHLHE40	chr18:28979771-28979805	K562	blood:	n/a	n/a
25	BHLHE40	chr18:29004392-29004670	HepG2	liver:	n/a	n/a
26	BHLHE40	chr18:29003291-29003573	HepG2	liver:	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	CBX3	chr18:29033979-29034622	HCT-116	colon:	n/a	n/a
30	CCNT2	chr18:28999563-28999620	K562	blood:	n/a	n/a
31	CEBPB	chr18:29019853-29020186	HepG2	liver:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
32	CEBPB	chr18:28979105-28980269	HCT-116	colon:	n/a	n/a
33	CEBPB	chr18:29019860-29020209	IMR90	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
34	CEBPB	chr18:28979724-28979929	HepG2	liver:	n/a	n/a
35	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
36	CEBPB	chr18:29049774-29049964	HepG2	liver:	n/a	chr18:29049873-29049884
37	CEBPB	chr18:28972607-28972963	Hela-S3	cervix:	n/a	n/a
38	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
39	CEBPB	chr18:28975048-28975251	H1-hESC	embryonic stem cell:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
40	CEBPB	chr18:29034088-29034345	A549	lung:	n/a	n/a
41	CEBPB	chr18:28981969-28982182	A549	lung:	n/a	n/a
42	CEBPB	chr18:28981474-28982350	HepG2	liver:	n/a	n/a
43	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
44	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
45	CEBPB	chr18:29025928-29026244	K562	blood:	n/a	n/a
46	CEBPB	chr18:28974947-28975271	K562	blood:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
47	CEBPB	chr18:28979290-28980148	HCT-116	colon:	n/a	n/a
48	CEBPB	chr18:28974940-28975186	A549	lung:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
49	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
50	CEBPB	chr18:29019854-29020182	A549	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29027701-29027751	HCM	heart:	n/a
2	chr18:29026301-29026351	CMK	blood:	n/a
3	chr18:29027745-29027795	AG04449	skin:	fetal
4	chr18:29027885-29027935	SK-N-MC	brain:	n/a
5	chr18:29027745-29027795	SK-N-SH_RA	brain:	n/a
6	chr18:29027745-29027795	SK-N-SH	brain:	n/a
7	chr18:29027701-29027751	BE2_C	brain:	n/a
8	chr18:29027658-29027708	T-47D	breast:	n/a
9	chr18:29026303-29026353	AoSMC	blood vessel:	n/a
10	chr18:29027745-29027795	HEK293	kidney:	embryo
11	chr18:29027658-29027708	NH-A	brain:	n/a
12	chr18:29027658-29027708	PANC-1	pancreas:	n/a
13	chr18:29027885-29027935	HIPEpiC	eye:	n/a
14	chr18:29026301-29026351	H1-hESC	embryonic stem cell:	embryo
15	chr18:29027658-29027708	HPAEpiC	pulmonary alveolar:	n/a
16	chr18:29026303-29026353	HEK293	kidney:	embryo
17	chr18:29027701-29027751	Caco-2	colon:	n/a
18	chr18:29027885-29027935	HCPEpiC	choroid plexus:	n/a
19	chr18:29026303-29026353	AG10803	skin:	n/a
20	chr18:29027658-29027708	K562	blood:	n/a
21	chr18:29027745-29027795	CMK	blood:	n/a
22	chr18:29026303-29026353	A549	lung:	n/a
23	chr18:29027745-29027795	PrEC	prostate:	n/a
24	chr18:29026301-29026351	HL-60	blood:	n/a
25	chr18:29027745-29027795	HCF	heart:	n/a
26	chr18:29027701-29027751	AoSMC	blood vessel:	n/a
27	chr18:29026303-29026353	HL-60	blood:	n/a
28	chr18:29026301-29026351	HRPEpiC	eye:	n/a
29	chr18:29026301-29026351	AG09309	skin:	n/a
30	chr18:29026301-29026351	HCM	heart:	n/a
31	chr18:29027885-29027935	NHBE	bronchial:	n/a
32	chr18:29027745-29027795	NHDF-neo	bronchial:	n/a
33	chr18:29027745-29027795	HRCEpiC	kidney:	n/a
34	chr18:29027701-29027751	A549	lung:	n/a
35	chr18:29027745-29027795	HCM	heart:	n/a
36	chr18:29027745-29027795	Jurkat	blood:	n/a
37	chr18:29027701-29027751	NH-A	brain:	n/a
38	chr18:29027885-29027935	SKMC	muscle:	n/a
39	chr18:29027885-29027935	HRE	kidney:	n/a
40	chr18:29027658-29027708	HCF	heart:	n/a
41	chr18:29026303-29026353	BJ	skin:	n/a
42	chr18:29027885-29027935	HUVEC	blood vessel:	n/a
43	chr18:29027658-29027708	AG09319	gingival:	n/a
44	chr18:29027885-29027935	LNCaP	prostate:	n/a
45	chr18:29027658-29027708	LNCaP	prostate:	n/a
46	chr18:29027885-29027935	AoSMC	blood vessel:	n/a
47	chr18:29027885-29027935	IMR90	lung:	fetal
48	chr18:29027885-29027935	PFSK-1	brain:	n/a
49	chr18:29027701-29027751	HUVEC	blood vessel:	n/a
50	chr18:29027745-29027795	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
2	chr18:28971505..28973722-chr18:28976105..28978957,2	K562	blood:
3	chr18:29004062..29004974-chr18:29135505..29136292,3	MCF-7	breast:
4	chr18:28980664..28983039-chr18:28984918..28986737,2	MCF-7	breast:
5	chr18:28971505..28973722-chr18:28976105..28978957,2	K562	blood:
6	chr18:29038234..29040822-chr18:29041279..29043976,2	MCF-7	breast:
7	chr18:29001628..29005715-chr18:29006148..29009419,4	K562	blood:
8	chr18:29046909..29049478-chr18:29076853..29079838,2	K562	blood:
9	chr18:29003549..29006106-chr18:29084281..29086820,2	MCF-7	breast:
10	chr18:29056016..29057570-chr18:29059465..29061281,2	K562	blood:
11	chr18:29044429..29046768-chr18:29048309..29050870,3	K562	blood:
12	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
13	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
14	chr18:29002388..29006763-chr18:29077410..29081754,4	K562	blood:
15	chr18:29004154..29005000-chr18:29143490..29144004,2	K562	blood:
16	chr18:29004133..29005005-chr18:29399717..29400321,2	K562	blood:
17	chr18:28786778..28788708-chr18:29017378..29018896,2	MCF-7	breast:
18	chr18:29003994..29005325-chr18:29086073..29087125,6	MCF-7	breast:
19	chr18:29003997..29005002-chr18:29143774..29144455,3	MCF-7	breast:
20	chr18:28821484..28823254-chr18:29002472..29004133,2	K562	blood:
21	chr18:29038496..29040369-chr18:29042094..29044336,2	K562	blood:
22	chr18:29003931..29004668-chr18:29134416..29135171,2	MCF-7	breast:
23	chr18:29038496..29040369-chr18:29042094..29044336,2	K562	blood:
24	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
25	chr18:29042545..29045965-chr18:29077171..29079744,3	K562	blood:
26	chr18:29044429..29046768-chr18:29048309..29050870,3	K562	blood:
27	chr18:29038234..29040822-chr18:29041279..29043976,2	MCF-7	breast:

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
DSG3	TF binding region
ENSG00000266729	TF binding region
DSG3	CpG island
ENSG00000266729	CpG island
ENSG00000266729	chromatin interactions
ENSG00000266521	chromatin interactions
ENSG00000046604	chromatin interactions

Extended variants
information (count: 3665 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3665 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9946169	chr18:28969044-28969045	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374759265	chr18:28969046-28969047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546603536	chr18:28969055-28969056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541994591	chr18:28969099-28969100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538933300	chr18:28969106-28969107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189844610	chr18:28969170-28969171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569045832	chr18:28969198-28969199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368808933	chr18:28969236-28969237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543287071	chr18:28969241-28969242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536011215	chr18:28969269-28969270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555849669	chr18:28969271-28969272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574014795	chr18:28969315-28969316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368872992	chr18:28969380-28969381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111988881	chr18:28969428-28969429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114387896	chr18:28969435-28969436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182914845	chr18:28969473-28969474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73410279	chr18:28969531-28969532	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs545287439	chr18:28969536-28969537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563599041	chr18:28969609-28969610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373505154	chr18:28969618-28969619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs60100528	chr18:28969634-28969635	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs187512381	chr18:28969664-28969665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9946737	chr18:28969668-28969669	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs528153409	chr18:28969721-28969722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546666888	chr18:28969776-28969777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368454876	chr18:28969784-28969785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191434635	chr18:28969791-28969792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148511161	chr18:28969809-28969810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141862703	chr18:28969840-28969841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569026122	chr18:28969842-28969843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536459488	chr18:28969856-28969857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182807658	chr18:28969859-28969860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561700610	chr18:28969929-28969930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188831689	chr18:28969938-28969939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534788185	chr18:28969952-28969953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs117830043	chr18:28969979-28969980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577624041	chr18:28970067-28970068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544974016	chr18:28970109-28970110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7233718	chr18:28970147-28970148	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs76019263	chr18:28970156-28970157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560429768	chr18:28970203-28970204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61277413	chr18:28970252-28970253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192154517	chr18:28970421-28970422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561323505	chr18:28970423-28970424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185032327	chr18:28970431-28970432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540342333	chr18:28970434-28970435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187840215	chr18:28970457-28970458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113618257	chr18:28970514-28970515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs16961779	chr18:28970525-28970526	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs550557978	chr18:28970539-28970540	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:367 , 50 per page) page: 1 2 3 4 5 6 7 8

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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