Variant report

Variant	esv3418813
Chromosome Location	chr18:44337754-44339752
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:8)
CpG islands
(count:369)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:8 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTBP2	chr18:44337460-44338259	H1-hESC	embryonic stem cell:	n/a	n/a
2	JUND	chr18:44337854-44338226	H1-hESC	embryonic stem cell:	n/a	n/a
3	MAX	chr18:44337374-44337780	A549	lung:	n/a	chr18:44337712-44337722
4	POLR2A	chr18:44337378-44338151	H1-neurons	neurons:	n/a	n/a
5	POLR2A	chr18:44337449-44338015	H1-neurons	neurons:	n/a	n/a
6	RAD21	chr18:44337631-44337863	H1-hESC	embryonic stem cell:	n/a	n/a
7	SIN3A	chr18:44337475-44338191	H1-hESC	embryonic stem cell:	n/a	n/a
8	ZNF384	chr18:44338412-44338423	K562	blood:	n/a	n/a

(count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44338099-44338149	HAEpiC	amniotic membrane:	n/a
2	chr18:44339513-44339563	GM12891	blood:	n/a
3	chr18:44338147-44338197	GM12878	blood:	n/a
4	chr18:44338099-44338149	HAEpiC	amniotic membrane:	n/a
5	chr18:44339513-44339563	GM12891	blood:	n/a
6	chr18:44338147-44338197	GM12878	blood:	n/a
7	chr18:44338147-44338197	SAEC	small airway:	n/a
8	chr18:44338099-44338149	GM06990	blood:	n/a
9	chr18:44337910-44337960	PrEC	prostate:	n/a
10	chr18:44337910-44337960	Jurkat	blood:	n/a
11	chr18:44337853-44337903	HMEC	breast:	n/a
12	chr18:44337922-44337972	GM12878	blood:	n/a
13	chr18:44337910-44337960	AG04450	lung:	fetal
14	chr18:44337922-44337972	HepG2	liver:	n/a
15	chr18:44338147-44338197	HEK293	kidney:	embryo
16	chr18:44339513-44339563	Hepatocyte	liver:	n/a
17	chr18:44339513-44339563	GM12892	blood:	n/a
18	chr18:44337922-44337972	U87	brain:	n/a
19	chr18:44338147-44338197	ovcar-3	ovarian:	n/a
20	chr18:44337910-44337960	GM12878	blood:	n/a
21	chr18:44337853-44337903	SK-N-MC	brain:	n/a
22	chr18:44337922-44337972	SAEC	small airway:	n/a
23	chr18:44338147-44338197	HAEpiC	amniotic membrane:	n/a
24	chr18:44339513-44339563	HEK293	kidney:	embryo
25	chr18:44337853-44337903	BE2_C	brain:	n/a
26	chr18:44339513-44339563	PANC-1	pancreas:	n/a
27	chr18:44338147-44338197	HCPEpiC	choroid plexus:	n/a
28	chr18:44337910-44337960	GM12891	blood:	n/a
29	chr18:44338147-44338197	T-47D	breast:	n/a
30	chr18:44337922-44337972	HRCEpiC	kidney:	n/a
31	chr18:44337922-44337972	HMEC	breast:	n/a
32	chr18:44338099-44338149	HUVEC	blood vessel:	n/a
33	chr18:44338147-44338197	CMK	blood:	n/a
34	chr18:44337922-44337972	NT2-D1	testis:	n/a
35	chr18:44338099-44338149	HNPCEpiC	eye:	n/a
36	chr18:44337910-44337960	SKMC	muscle:	n/a
37	chr18:44338099-44338149	HCPEpiC	choroid plexus:	n/a
38	chr18:44338099-44338149	Hela-S3	cervix:	n/a
39	chr18:44337922-44337972	SK-N-SH_RA	brain:	n/a
40	chr18:44337922-44337972	AG04450	lung:	fetal
41	chr18:44339513-44339563	AG09319	gingival:	n/a
42	chr18:44339513-44339563	NB4	blood:	n/a
43	chr18:44337853-44337903	HepG2	liver:	n/a
44	chr18:44337922-44337972	HRE	kidney:	n/a
45	chr18:44338099-44338149	SKMC	muscle:	n/a
46	chr18:44337922-44337972	HIPEpiC	eye:	n/a
47	chr18:44338147-44338197	HepG2	liver:	n/a
48	chr18:44339513-44339563	GM12878	blood:	n/a
49	chr18:44337910-44337960	HCT-116	colon:	n/a
50	chr18:44337922-44337972	NHBE	bronchial:	n/a

No data

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KATNAL2-1	chr18:44337689-44338426	NONHSAT059140
2	lnc-KATNAL2-1	chr18:44338764-44339028	NONHSAT059140
3	lnc-KATNAL2-1	chr18:44339687-44344371	NONHSAT059142
4	lnc-KATNAL2-1	chr18:44338415-44338422	XLOC_012667

No data

Variant related genes	Relation type
ST8SIA5	TF binding region
ST8SIA5	CpG island

Extended variants
information (count: 49 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:49 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138697490	chr18:44337760-44337761	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs370603825	chr18:44337794-44337795	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs571992375	chr18:44337805-44337806	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs540954538	chr18:44337823-44337824	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs561331064	chr18:44337833-44337834	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs538044304	chr18:44337837-44337838	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs72903352	chr18:44337870-44337871	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region CpG island lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs550205447	chr18:44337879-44337880	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs563631334	chr18:44337939-44337940	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs183471803	chr18:44337949-44337950	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs552817701	chr18:44337957-44337958	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs566307466	chr18:44337984-44337985	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs535333950	chr18:44337992-44337993	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs548943649	chr18:44338008-44338009	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs567215164	chr18:44338009-44338010	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs535874381	chr18:44338070-44338071	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs556196009	chr18:44338071-44338072	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs3809961	chr18:44338072-44338073	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs538381956	chr18:44338158-44338159	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs73434973	chr18:44338209-44338210	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs377645169	chr18:44338223-44338224	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs3809962	chr18:44338245-44338246	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs540917900	chr18:44338285-44338286	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs561034738	chr18:44338393-44338394	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs73953884	chr18:44338394-44338395	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs553775946	chr18:44338429-44338430	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs11661172	chr18:44338430-44338431	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs371355571	chr18:44338434-44338435	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs557777248	chr18:44338546-44338547	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs577745662	chr18:44338547-44338548	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs532632454	chr18:44338613-44338614	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs546368252	chr18:44338615-44338616	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs577450008	chr18:44338691-44338692	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs190415909	chr18:44338710-44338711	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs75017403	chr18:44338747-44338748	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs78742175	chr18:44338750-44338751	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs75225570	chr18:44338751-44338752	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs80338448	chr18:44338754-44338755	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs35271871	chr18:44338868-44338869	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	lncRNA	n/a	Overlapped CNVs	n/a
40	rs542060562	chr18:44338895-44338896	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	lncRNA	n/a	Overlapped CNVs	n/a
41	rs372258670	chr18:44338899-44338900	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	lncRNA	n/a	Overlapped CNVs	n/a
42	rs9965325	chr18:44338936-44338937	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	lncRNA	n/a	Overlapped CNVs	n/a
43	rs182349156	chr18:44338955-44338956	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	lncRNA	n/a	Overlapped CNVs	n/a
44	rs529659472	chr18:44339314-44339315	Weak transcription Enhancers Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs185342544	chr18:44339425-44339426	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs115494959	chr18:44339561-44339562	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs115496111	chr18:44339583-44339584	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs538342996	chr18:44339594-44339595	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs558271035	chr18:44339644-44339645	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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

Chromatin state (count:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44334200-44337800	Active TSS	Brain Angular Gyrus	brain
2	chr18:44334400-44338000	Active TSS	Brain Inferior Temporal Lobe	brain
3	chr18:44334400-44338400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
4	chr18:44335000-44337800	Active TSS	HSMMtube	muscle
5	chr18:44335200-44338200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr18:44335400-44338200	Active TSS	HSMM	muscle
7	chr18:44335400-44338200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
8	chr18:44335600-44337800	Active TSS	Brain Substantia Nigra	brain
9	chr18:44335600-44338000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr18:44335600-44338000	Bivalent/Poised TSS	NHDF-Ad	bronchial
11	chr18:44335600-44338200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr18:44335600-44338200	Active TSS	Brain Cingulate Gyrus	brain
13	chr18:44335800-44338000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
14	chr18:44335800-44338000	Active TSS	Psoas Muscle	Psoas
15	chr18:44335800-44338200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
16	chr18:44335800-44338200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
17	chr18:44335800-44338400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
18	chr18:44335800-44338400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
19	chr18:44335800-44338400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
20	chr18:44336000-44337800	Active TSS	Brain Anterior Caudate	brain
21	chr18:44336000-44338000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
22	chr18:44336000-44338000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
23	chr18:44336000-44338000	Active TSS	Left Ventricle	heart
24	chr18:44336000-44338200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
25	chr18:44336000-44338400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
26	chr18:44336200-44337800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
27	chr18:44336200-44337800	Bivalent Enhancer	Fetal Brain Male	brain
28	chr18:44336200-44338200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr18:44336200-44338200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr18:44336200-44338200	Bivalent Enhancer	Lung	lung
31	chr18:44336200-44338200	Enhancers	Pancreas	Pancrea
32	chr18:44336200-44338200	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
33	chr18:44336200-44338200	Bivalent Enhancer	Spleen	Spleen
34	chr18:44336400-44337800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr18:44336400-44337800	Bivalent/Poised TSS	NHLF	lung
36	chr18:44336400-44338200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr18:44336600-44337800	Bivalent/Poised TSS	NH-A	brain
38	chr18:44336600-44338000	Bivalent/Poised TSS	Thymus	Thymus
39	chr18:44336600-44338200	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr18:44336800-44337800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr18:44336800-44338000	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr18:44336800-44338200	Bivalent/Poised TSS	A549	lung
43	chr18:44337000-44337800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
44	chr18:44337000-44338000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
45	chr18:44337000-44338000	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
46	chr18:44337000-44338200	Bivalent Enhancer	Placenta	Placenta
47	chr18:44337000-44338400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
48	chr18:44337200-44337800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
49	chr18:44337200-44338200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr18:44337400-44337800	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived

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