Variant report

Variant	nsv909610
Chromosome Location	chr18:44549455-44602249
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:735)
CpG islands
(count:1588)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:44576874-44576992	K562	blood:	n/a	n/a
2	ARID3A	chr18:44576810-44577094	HepG2	liver:	n/a	n/a
3	BCL11A	chr18:44555313-44555571	GM12878	blood:	n/a	n/a
4	BCL11A	chr18:44549353-44549656	GM12878	blood:	n/a	n/a
5	BHLHE40	chr18:44553731-44554022	HepG2	liver:	n/a	n/a
6	BHLHE40	chr18:44576859-44577090	GM12878	blood:	n/a	n/a
7	BHLHE40	chr18:44552793-44553372	HepG2	liver:	n/a	n/a
8	BRCA1	chr18:44576815-44577084	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr18:44562609-44562949	HCT-116	colon:	n/a	n/a
10	CEBPB	chr18:44589464-44589717	HepG2	liver:	n/a	chr18:44589609-44589622 chr18:44589610-44589621
11	CEBPB	chr18:44569502-44569627	K562	blood:	n/a	n/a
12	CHD2	chr18:44601544-44602123	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr18:44576900-44577050	HCT-116	colon:	n/a	chr18:44577006-44577014
14	CTCF	chr18:44562740-44562890	GM12865	blood:	n/a	n/a
15	CTCF	chr18:44577140-44577290	WERI-Rb-1	eye:	n/a	n/a
16	CTCF	chr18:44562440-44562590	HVMF	connective:	n/a	n/a
17	CTCF	chr18:44576860-44577010	GM12871	blood:	n/a	n/a
18	CTCF	chr18:44576880-44577030	HUVEC	blood vessel:	n/a	chr18:44577006-44577014
19	CTCF	chr18:44576880-44577030	WI-38	lung:	n/a	chr18:44577006-44577014
20	CTCF	chr18:44562643-44563045	K562	blood:	n/a	n/a
21	CTCF	chr18:44562760-44562910	HCFaa	heart:	n/a	n/a
22	CTCF	chr18:44576820-44576970	GM12868	blood:	n/a	n/a
23	CTCF	chr18:44562780-44562930	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr18:44562760-44562910	GM12873	blood:	n/a	n/a
25	CTCF	chr18:44576700-44576850	A549	lung:	n/a	n/a
26	CTCF	chr18:44576860-44577010	GM12875	blood:	n/a	n/a
27	CTCF	chr18:44562740-44562890	GM12872	blood:	n/a	n/a
28	CTCF	chr18:44562780-44562930	GM12864	blood:	n/a	n/a
29	CTCF	chr18:44576824-44577056	K562	blood:	n/a	chr18:44577006-44577014
30	CTCF	chr18:44557210-44557657	K562	blood:	n/a	n/a
31	CTCF	chr18:44576820-44576970	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr18:44562680-44562830	NHLF	lung:	n/a	n/a
33	CTCF	chr18:44556001-44556074	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr18:44562742-44562951	HepG2	liver:	n/a	n/a
35	CTCF	chr18:44550232-44550622	K562	blood:	n/a	n/a
36	CTCF	chr18:44557429-44557536	LNCaP	prostate:	n/a	n/a
37	CTCF	chr18:44576820-44577070	GM12878	blood:	n/a	chr18:44577006-44577014
38	CTCF	chr18:44562780-44562930	GM06990	blood:	n/a	n/a
39	CTCF	chr18:44562760-44562910	HCT-116	colon:	n/a	n/a
40	CTCF	chr18:44576880-44577030	HEEpiC	esophagus:	n/a	chr18:44577006-44577014
41	CTCF	chr18:44576825-44577058	Pancreas_OC	pancreas:	n/a	chr18:44577006-44577014
42	CTCF	chr18:44577240-44577390	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr18:44551620-44551770	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr18:44576880-44577030	BE2_C	brain:	n/a	chr18:44577006-44577014
45	CTCF	chr18:44576880-44577030	Hela-S3	cervix:	n/a	chr18:44577006-44577014
46	CTCF	chr18:44561420-44561449	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr18:44576840-44576990	GM12864	blood:	n/a	n/a
48	CTCF	chr18:44576900-44577050	HFF	foreskin:	n/a	chr18:44577006-44577014
49	CTCF	chr18:44562733-44562959	MCF-7	breast:	n/a	n/a
50	CTCF	chr18:44551296-44551735	K562	blood:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44551732-44551782	GM12878	blood:	n/a
2	chr18:44562030-44562080	SKMC	muscle:	n/a
3	chr18:44551732-44551782	GM12878	blood:	n/a
4	chr18:44562030-44562080	SKMC	muscle:	n/a
5	chr18:44555308-44555358	GM06990	blood:	n/a
6	chr18:44555308-44555358	A549	lung:	n/a
7	chr18:44562056-44562106	GM06990	blood:	n/a
8	chr18:44557647-44557697	GM06990	blood:	n/a
9	chr18:44551732-44551782	NHDF-neo	bronchial:	n/a
10	chr18:44557732-44557782	AG04450	lung:	fetal
11	chr18:44562063-44562113	HUVEC	blood vessel:	n/a
12	chr18:44551719-44551769	HL-60	blood:	n/a
13	chr18:44561130-44561180	HRPEpiC	eye:	n/a
14	chr18:44561718-44561768	GM12892	blood:	n/a
15	chr18:44561725-44561775	ECC-1	luminal epithelium:	n/a
16	chr18:44561188-44561238	LNCaP	prostate:	n/a
17	chr18:44562113-44562163	HCF	heart:	n/a
18	chr18:44557635-44557685	AG10803	skin:	n/a
19	chr18:44562505-44562555	HCF	heart:	n/a
20	chr18:44562505-44562555	A549	lung:	n/a
21	chr18:44551719-44551769	HepG2	liver:	n/a
22	chr18:44557819-44557869	HRCEpiC	kidney:	n/a
23	chr18:44562019-44562069	HMEC	breast:	n/a
24	chr18:44557647-44557697	HNPCEpiC	eye:	n/a
25	chr18:44561385-44561435	NHDF-neo	bronchial:	n/a
26	chr18:44561385-44561435	Hela-S3	cervix:	n/a
27	chr18:44561385-44561435	NT2-D1	testis:	n/a
28	chr18:44564432-44564482	A549	lung:	n/a
29	chr18:44562030-44562080	HEEpiC	esophagus:	n/a
30	chr18:44562019-44562069	HEK293	kidney:	embryo
31	chr18:44557732-44557782	MCF10A-Er-Src	breast:	n/a
32	chr18:44562113-44562163	HUVEC	blood vessel:	n/a
33	chr18:44561725-44561775	HRE	kidney:	n/a
34	chr18:44557635-44557685	AG09309	skin:	n/a
35	chr18:44561130-44561180	AG10803	skin:	n/a
36	chr18:44562056-44562106	SK-N-SH	brain:	n/a
37	chr18:44562136-44562186	H1-hESC	embryonic stem cell:	embryo
38	chr18:44562019-44562069	MCF10A-Er-Src	breast:	n/a
39	chr18:44562136-44562186	HepG2	liver:	n/a
40	chr18:44557732-44557782	ProgFib	skin:	n/a
41	chr18:44555308-44555358	HRPEpiC	eye:	n/a
42	chr18:44562136-44562186	LNCaP	prostate:	n/a
43	chr18:44562918-44562968	GM12892	blood:	n/a
44	chr18:44562019-44562069	AG09309	skin:	n/a
45	chr18:44562063-44562113	GM12878	blood:	n/a
46	chr18:44561725-44561775	PANC-1	pancreas:	n/a
47	chr18:44557635-44557685	GM12878	blood:	n/a
48	chr18:44557732-44557782	K562	blood:	n/a
49	chr18:44557635-44557685	NH-A	brain:	n/a
50	chr18:44557819-44557869	HCPEpiC	choroid plexus:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:44576380..44577341-chr18:45275241..45276255,4	K562	blood:
2	chr18:44599383..44602020-chr18:44603317..44605439,2	K562	blood:
3	chr18:44576766..44577535-chr18:44731006..44731680,3	K562	blood:
4	chr18:44576733..44577369-chr18:44809595..44810437,2	K562	blood:
5	chr18:44580930..44582720-chr18:44583404..44586323,2	K562	blood:
6	chr18:44529742..44530665-chr18:44562546..44563169,2	MCF-7	breast:
7	chr18:44576795..44577462-chr18:44731213..44731981,2	MCF-7	breast:

No data

Variant related genes	Relation type
TCEB3B	TF binding region
TCEB3CL	TF binding region
TCEB3CL2	TF binding region
KATNAL2	TF binding region
TCEB3C	TF binding region
TCEB3B	CpG island
TCEB3CL	CpG island
TCEB3CL2	CpG island
KATNAL2	CpG island
TCEB3C	CpG island
ENSG00000167216	chromatin interactions

Extended variants
information (count: 1668 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1668 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56006467	chr18:44549455-44549456	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs201849084	chr18:44549539-44549540	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs142945452	chr18:44549607-44549608	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs151258432	chr18:44549653-44549654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150666856	chr18:44551344-44551345	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs563369682	chr18:44551399-44551400	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs139808744	chr18:44551433-44551434	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs372023027	chr18:44551468-44551469	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs370147805	chr18:44551469-44551470	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs372435314	chr18:44551476-44551477	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs57138556	chr18:44551477-44551478	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs371899372	chr18:44551478-44551479	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs62095396	chr18:44551481-44551482	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs140437548	chr18:44551629-44551630	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs146793049	chr18:44551710-44551711	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs373263125	chr18:44551718-44551719	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs550781818	chr18:44551770-44551771	Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs139462441	chr18:44551774-44551775	Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs139532054	chr18:44551873-44551874	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs375095195	chr18:44551874-44551875	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs138564494	chr18:44551881-44551882	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs142604536	chr18:44551893-44551894	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs146782275	chr18:44551916-44551917	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs573062788	chr18:44551918-44551919	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs143492223	chr18:44551954-44551955	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs528369375	chr18:44552013-44552014	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs548109979	chr18:44552153-44552154	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs568277263	chr18:44552246-44552247	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs112143049	chr18:44552364-44552365	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs149496990	chr18:44552427-44552428	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs530904129	chr18:44552444-44552445	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs550700161	chr18:44552445-44552446	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs145666122	chr18:44552449-44552450	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs539977443	chr18:44552475-44552476	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs143948116	chr18:44552484-44552485	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs112334011	chr18:44552568-44552569	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs564988487	chr18:44552580-44552581	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs143565528	chr18:44552856-44552857	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs3017165	chr18:44553082-44553083	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs142083065	chr18:44553245-44553246	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs148203353	chr18:44553265-44553266	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs145843449	chr18:44553300-44553301	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs145061583	chr18:44553365-44553366	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs141161610	chr18:44553376-44553377	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs544614376	chr18:44553380-44553381	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs375300564	chr18:44553381-44553382	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs553601802	chr18:44553382-44553383	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs113200308	chr18:44553390-44553391	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs567097134	chr18:44553736-44553737	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs536141456	chr18:44553810-44553811	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
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
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
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
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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
small cell lung cancer	17426248	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:145 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44538200-44551600	Weak transcription	Gastric	stomach
2	chr18:44545200-44552000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr18:44547400-44552000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr18:44547400-44552000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr18:44550200-44556600	Weak transcription	Fetal Lung	lung
6	chr18:44551600-44551800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr18:44551600-44551800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr18:44551800-44553000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr18:44551800-44553000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr18:44552000-44552200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr18:44552000-44552200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr18:44552000-44552400	Enhancers	H1 Cell Line	embryonic stem cell
13	chr18:44552000-44552400	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr18:44552000-44552400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr18:44552200-44552400	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr18:44552400-44555000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr18:44553000-44553200	Enhancers	Right Ventricle	heart
18	chr18:44553000-44553600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr18:44553000-44553600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr18:44553200-44562600	Weak transcription	Right Ventricle	heart
21	chr18:44553600-44554000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr18:44553600-44555000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr18:44554000-44555400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr18:44554000-44555400	ZNF genes & repeats	Stomach Smooth Muscle	stomach
25	chr18:44554600-44555400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
26	chr18:44555000-44555400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
27	chr18:44555000-44555400	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr18:44555000-44555400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
29	chr18:44555200-44555400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr18:44555400-44560000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr18:44555400-44560000	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr18:44555400-44561400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr18:44555400-44563200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr18:44560000-44560400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr18:44560000-44560600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
36	chr18:44561400-44561600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr18:44561600-44562000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr18:44561800-44562000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr18:44562600-44563200	Enhancers	GM12878-XiMat	blood
40	chr18:44563200-44564000	Flanking Active TSS	GM12878-XiMat	blood
41	chr18:44564000-44564600	Enhancers	GM12878-XiMat	blood
42	chr18:44574600-44577000	Weak transcription	Brain Anterior Caudate	brain
43	chr18:44577000-44577400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr18:44577000-44577400	Enhancers	Brain Angular Gyrus	brain
45	chr18:44577000-44577400	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr18:44577400-44594000	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr18:44579800-44630200	Weak transcription	Right Ventricle	heart
48	chr18:44580200-44580400	Enhancers	H9 Cell Line	embryonic stem cell
49	chr18:44580200-44581400	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr18:44580200-44581600	Enhancers	Skeletal Muscle Female	skeletal muscle

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