Variant report

Variant	esv1819321
Chromosome Location	chr18:43909994-43930972
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:459)
CpG islands
(count:856)
Chromatin interactive
region (count:6)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:459 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr18:43923955-43924431	GM12878	blood:	n/a	n/a
2	ATF2	chr18:43915419-43915953	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr18:43915397-43915847	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr18:43923959-43924320	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr18:43914321-43914352	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr18:43912950-43914058	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr18:43918187-43918248	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr18:43915493-43916016	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr18:43924025-43924312	GM12878	blood:	n/a	chr18:43924140-43924150 chr18:43924139-43924150
10	BHLHE40	chr18:43913455-43913716	HepG2	liver:	n/a	n/a
11	BHLHE40	chr18:43913571-43913771	GM12878	blood:	n/a	n/a
12	BHLHE40	chr18:43923859-43924179	GM12878	blood:	n/a	n/a
13	BHLHE40	chr18:43923726-43923956	K562	blood:	n/a	chr18:43923739-43923748
14	BRCA1	chr18:43914350-43914357	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr18:43915162-43916347	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr18:43916642-43917020	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr18:43912864-43912905	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr18:43915438-43916123	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr18:43914858-43915184	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr18:43915897-43915938	IMR90	lung:	n/a	n/a
21	CEBPB	chr18:43911341-43911698	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr18:43911342-43911682	HepG2	liver:	n/a	n/a
23	CEBPB	chr18:43913479-43914028	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr18:43915408-43916093	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr18:43911467-43911616	K562	blood:	n/a	n/a
26	CHD1	chr18:43915183-43915600	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr18:43918343-43918352	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr18:43923848-43924439	GM12878	blood:	n/a	n/a
29	CHD2	chr18:43913251-43914211	Hela-S3	cervix:	n/a	chr18:43913992-43913999 chr18:43914023-43914030
30	CHD2	chr18:43915321-43915921	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr18:43916950-43917034	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr18:43925371-43925386	GM12878	blood:	n/a	n/a
33	CHD2	chr18:43914415-43916091	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr18:43924028-43924226	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTBP2	chr18:43914886-43916057	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr18:43918320-43918470	SK-N-SH_RA	brain:	n/a	chr18:43918359-43918372 chr18:43918357-43918375
37	CTCF	chr18:43913720-43913870	SAEC	small airway:	n/a	n/a
38	CTCF	chr18:43924080-43924230	HMEC	breast:	n/a	chr18:43924154-43924162 chr18:43924147-43924160
39	CTCF	chr18:43924088-43924218	GM12891	blood:	n/a	chr18:43924154-43924162 chr18:43924147-43924160
40	CTCF	chr18:43913744-43913746	MCF-7	breast:	n/a	n/a
41	CTCF	chr18:43923940-43924090	GM06990	blood:	n/a	n/a
42	CTCF	chr18:43924073-43924237	GM12892	blood:	n/a	chr18:43924154-43924162 chr18:43924147-43924160
43	CTCF	chr18:43918320-43918470	BE2_C	brain:	n/a	chr18:43918359-43918372 chr18:43918357-43918375
44	CTCF	chr18:43924238-43924242	GM19238	blood:	n/a	n/a
45	CTCF	chr18:43923892-43924049	GM19239	blood:	n/a	n/a
46	CTCF	chr18:43918280-43918430	HEK293	kidney:	n/a	chr18:43918359-43918372 chr18:43918357-43918375
47	CTCF	chr18:43923924-43924064	MCF-7	breast:	n/a	n/a
48	CTCF	chr18:43923920-43924150	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr18:43923980-43924130	HRE	kidney:	n/a	n/a
50	CTCF	chr18:43924140-43924290	GM12864	blood:	n/a	chr18:43924154-43924162 chr18:43924147-43924160

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:43913346-43913396	U87	brain:	n/a
2	chr18:43913147-43913197	HCF	heart:	n/a
3	chr18:43913346-43913396	U87	brain:	n/a
4	chr18:43913147-43913197	HCF	heart:	n/a
5	chr18:43913565-43913615	HAEpiC	amniotic membrane:	n/a
6	chr18:43912991-43913041	HNPCEpiC	eye:	n/a
7	chr18:43913147-43913197	HAEpiC	amniotic membrane:	n/a
8	chr18:43917496-43917546	HRCEpiC	kidney:	n/a
9	chr18:43913565-43913615	H1-hESC	embryonic stem cell:	embryo
10	chr18:43913649-43913699	SK-N-SH	brain:	n/a
11	chr18:43917496-43917546	PANC-1	pancreas:	n/a
12	chr18:43913719-43913769	SK-N-SH	brain:	n/a
13	chr18:43915901-43915951	SAEC	small airway:	n/a
14	chr18:43913565-43913615	ovcar-3	ovarian:	n/a
15	chr18:43913565-43913615	U87	brain:	n/a
16	chr18:43913755-43913805	ECC-1	luminal epithelium:	n/a
17	chr18:43914226-43914276	U87	brain:	n/a
18	chr18:43913147-43913197	BE2_C	brain:	n/a
19	chr18:43917496-43917546	ProgFib	skin:	n/a
20	chr18:43913755-43913805	GM19239	blood:	n/a
21	chr18:43914047-43914097	NHBE	bronchial:	n/a
22	chr18:43914047-43914097	AG10803	skin:	n/a
23	chr18:43912991-43913041	SK-N-SH_RA	brain:	n/a
24	chr18:43913565-43913615	NHDF-neo	bronchial:	n/a
25	chr18:43913346-43913396	HUVEC	blood vessel:	n/a
26	chr18:43914047-43914097	GM12892	blood:	n/a
27	chr18:43913649-43913699	Jurkat	blood:	n/a
28	chr18:43913719-43913769	Jurkat	blood:	n/a
29	chr18:43914226-43914276	MCF10A-Er-Src	breast:	n/a
30	chr18:43914226-43914276	HMEC	breast:	n/a
31	chr18:43914264-43914314	GM06990	blood:	n/a
32	chr18:43913649-43913699	GM06990	blood:	n/a
33	chr18:43913649-43913699	PrEC	prostate:	n/a
34	chr18:43913719-43913769	GM12891	blood:	n/a
35	chr18:43913565-43913615	GM19239	blood:	n/a
36	chr18:43914047-43914097	HUVEC	blood vessel:	n/a
37	chr18:43913346-43913396	AG09309	skin:	n/a
38	chr18:43913755-43913805	HPAEpiC	pulmonary alveolar:	n/a
39	chr18:43913147-43913197	T-47D	breast:	n/a
40	chr18:43913755-43913805	HCF	heart:	n/a
41	chr18:43914226-43914276	ProgFib	skin:	n/a
42	chr18:43913699-43913749	HUVEC	blood vessel:	n/a
43	chr18:43913565-43913615	SK-N-MC	brain:	n/a
44	chr18:43913699-43913749	HRE	kidney:	n/a
45	chr18:43913755-43913805	HCM	heart:	n/a
46	chr18:43915901-43915951	Hepatocyte	liver:	n/a
47	chr18:43912991-43913041	HEEpiC	esophagus:	n/a
48	chr18:43914264-43914314	HRE	kidney:	n/a
49	chr18:43912991-43913041	AG04449	skin:	fetal
50	chr18:43914226-43914276	HCPEpiC	choroid plexus:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:43751486..43754394-chr18:43913234..43915228,2	MCF-7	breast:
2	chr18:43922751..43924644-chr18:43951049..43953922,2	MCF-7	breast:
3	chr18:43912706..43915480-chr18:43919399..43921708,3	MCF-7	breast:
4	chr18:43912035..43913739-chr18:43924023..43926965,2	MCF-7	breast:
5	chr18:43908257..43911252-chr18:43912177..43914068,3	MCF-7	breast:
6	chr18:43912035..43913739-chr18:43924023..43926965,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF165-1	chr18:43914206-43914298	NONHSAT059132
2	lnc-RNF165-1	chr18:43914187-43914298	NR_046357
3	lnc-RNF165-1	chr18:43913931-43914088	NONHSAT059132
4	lnc-RNF165-1	chr18:43915851-43917614	NR_046357
5	lnc-LOXHD1-1	chr18:43916080-43917171	ENSG00000248078
6	lnc-RNF165-1	chr18:43915856-43917609	NONHSAT059132
7	lnc-LOXHD1-1	chr18:43914928-43915292	ENSG00000248078

No data

Variant related genes	Relation type
RNF165	TF binding region
RNF165	CpG island
ENSG00000141622	chromatin interactions
ENSG00000152242	chromatin interactions
HAND1	miRNA target sites
RAB7L1	miRNA target sites

Extended variants
information (count: 800 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:800 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6507696	chr18:43909994-43909995	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557354364	chr18:43909998-43909999	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs115228702	chr18:43910004-43910005	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs183453873	chr18:43910038-43910039	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs78669187	chr18:43910100-43910101	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs16978541	chr18:43910108-43910109	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs372704184	chr18:43910120-43910121	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs540322803	chr18:43910202-43910203	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs571427384	chr18:43910207-43910208	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs144574851	chr18:43910250-43910251	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs147460534	chr18:43910315-43910316	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs562607974	chr18:43910358-43910359	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs189235476	chr18:43910361-43910362	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs193075806	chr18:43910365-43910366	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs8098098	chr18:43910422-43910423	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs560378602	chr18:43910444-43910445	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs527430017	chr18:43910479-43910480	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549076539	chr18:43910485-43910486	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs567286812	chr18:43910487-43910488	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs537406505	chr18:43910520-43910521	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs185408515	chr18:43910584-43910585	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs139730188	chr18:43910634-43910635	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs142714241	chr18:43910649-43910650	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs540031676	chr18:43910659-43910660	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs75103940	chr18:43910693-43910694	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs573101329	chr18:43910698-43910699	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs8098503	chr18:43910737-43910738	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs141153885	chr18:43910755-43910756	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201042995	chr18:43910810-43910811	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs11082520	chr18:43910811-43910812	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs555427835	chr18:43910815-43910816	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs35104842	chr18:43910825-43910826	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs114832106	chr18:43910869-43910870	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs7232125	chr18:43910908-43910909	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs556426624	chr18:43911030-43911031	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs577821222	chr18:43911113-43911114	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs113276041	chr18:43911115-43911116	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs545319050	chr18:43911178-43911179	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs560417228	chr18:43911190-43911191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs527465135	chr18:43911281-43911282	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs150978403	chr18:43911311-43911312	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs560792154	chr18:43911364-43911365	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs531336839	chr18:43911443-43911444	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs11082521	chr18:43911448-43911449	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs72907334	chr18:43911545-43911546	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs533494161	chr18:43911546-43911547	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs551639323	chr18:43911567-43911568	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs537368810	chr18:43911606-43911607	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs11082522	chr18:43911621-43911622	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs56958501	chr18:43911658-43911659	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
low-grade B-cell lymphoma tumor	18367492	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
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	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
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:972 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:43906000-43912400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr18:43906000-43912400	Weak transcription	Hela-S3	cervix
3	chr18:43909800-43910000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr18:43909800-43910000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr18:43909800-43910000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr18:43909800-43910000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr18:43910000-43910400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr18:43911000-43912600	Enhancers	Liver	Liver
9	chr18:43911200-43911600	Enhancers	HepG2	liver
10	chr18:43911200-43911600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
11	chr18:43911400-43911600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
12	chr18:43911600-43912000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr18:43912200-43912800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr18:43912200-43913200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr18:43912400-43912800	Enhancers	Hela-S3	cervix
16	chr18:43912400-43913000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr18:43912400-43913000	Enhancers	Fetal Brain Male	brain
18	chr18:43912400-43913000	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr18:43912400-43913200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr18:43912400-43913400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr18:43912400-43913400	Enhancers	Right Ventricle	heart
22	chr18:43912600-43912800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr18:43912600-43912800	Enhancers	Fetal Brain Female	brain
24	chr18:43912600-43912800	Enhancers	Dnd41	blood
25	chr18:43912600-43913000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
26	chr18:43912600-43913200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
27	chr18:43912600-43913200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
28	chr18:43912600-43913200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr18:43912600-43913400	Enhancers	Placenta Amnion	Placenta Amnion
30	chr18:43912600-43913800	Flanking Active TSS	Liver	Liver
31	chr18:43912800-43913000	Enhancers	Brain Anterior Caudate	brain
32	chr18:43912800-43913000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
33	chr18:43912800-43913000	Enhancers	Brain Substantia Nigra	brain
34	chr18:43912800-43913000	Enhancers	Esophagus	oesophagus
35	chr18:43912800-43913000	Flanking Active TSS	Fetal Brain Female	brain
36	chr18:43912800-43913000	Enhancers	Fetal Heart	heart
37	chr18:43912800-43913200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
38	chr18:43912800-43913200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr18:43912800-43913200	Bivalent Enhancer	Fetal Lung	lung
40	chr18:43912800-43913200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr18:43912800-43913200	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr18:43912800-43913400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr18:43912800-43913400	Enhancers	Left Ventricle	heart
44	chr18:43912800-43913400	Enhancers	Pancreas	Pancrea
45	chr18:43912800-43913400	Enhancers	Right Atrium	heart
46	chr18:43912800-43913600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr18:43912800-43913600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr18:43912800-43913600	Flanking Active TSS	Hela-S3	cervix
49	chr18:43912800-43913800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
50	chr18:43912800-43913800	Flanking Active TSS	Dnd41	blood

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