Variant report

Variant	esv3345210
Chromosome Location	chr15:45402360-45405508
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:180)
CpG islands
(count:367)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:180 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr15:45404699-45405166	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD1	chr15:45405290-45405311	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTBP2	chr15:45404577-45407347	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr15:45402592-45402683	MCF-7	breast:	n/a	n/a
5	CTCF	chr15:45402320-45402470	A549	lung:	n/a	n/a
6	CTCF	chr15:45403680-45403830	SK-N-SH_RA	brain:	n/a	n/a
7	CTCF	chr15:45402525-45402732	GM12878	blood:	n/a	n/a
8	CTCF	chr15:45402600-45402750	HRPEpiC	eye:	n/a	n/a
9	CTCF	chr15:45402609-45402636	NHEK	skin:	n/a	n/a
10	CTCF	chr15:45402591-45402655	GM13976	blood:	n/a	n/a
11	CTCF	chr15:45402540-45402690	GM06990	blood:	n/a	n/a
12	CTCF	chr15:45402580-45402730	GM12875	blood:	n/a	n/a
13	CTCF	chr15:45402420-45402570	BJ	skin:	n/a	n/a
14	CTCF	chr15:45402560-45402710	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr15:45402580-45402730	GM12865	blood:	n/a	n/a
16	CTCF	chr15:45402540-45402690	GM12878	blood:	n/a	n/a
17	CTCF	chr15:45402580-45402730	HRPEpiC	eye:	n/a	n/a
18	CTCF	chr15:45402500-45402650	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr15:45402660-45402810	GM12864	blood:	n/a	n/a
20	CTCF	chr15:45403630-45403815	GM19239	blood:	n/a	n/a
21	CTCF	chr15:45402578-45402677	HepG2	liver:	n/a	n/a
22	CTCF	chr15:45403600-45403750	SAEC	small airway:	n/a	n/a
23	CTCF	chr15:45405420-45405570	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr15:45402600-45402750	HepG2	liver:	n/a	n/a
25	CTCF	chr15:45403489-45403549	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr15:45402460-45402750	HFF-Myc	foreskin:	n/a	n/a
27	CTCF	chr15:45402540-45402690	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr15:45403739-45403811	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr15:45403680-45403830	SAEC	small airway:	n/a	n/a
30	CTCF	chr15:45402560-45402710	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr15:45402785-45402917	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr15:45402526-45402709	HepG2	liver:	n/a	n/a
33	CTCF	chr15:45403660-45403810	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr15:45402607-45402707	GM20000	blood:	n/a	n/a
35	CTCF	chr15:45402550-45402672	K562	blood:	n/a	n/a
36	CTCF	chr15:45402520-45402670	HCFaa	heart:	n/a	n/a
37	CTCF	chr15:45402300-45402450	NB4	blood:	n/a	n/a
38	CTCF	chr15:45403649-45403881	GM12891	blood:	n/a	n/a
39	CTCF	chr15:45402560-45402710	HL-60	blood:	n/a	n/a
40	CTCF	chr15:45402540-45402690	NHEK	skin:	n/a	n/a
41	CTCF	chr15:45402520-45402670	GM12869	blood:	n/a	n/a
42	CTCF	chr15:45403630-45403848	NHEK	skin:	n/a	n/a
43	CTCF	chr15:45402520-45402670	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr15:45403459-45403485	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr15:45404700-45404850	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr15:45402540-45402690	GM12873	blood:	n/a	n/a
47	CTCF	chr15:45402540-45402690	AG09309	skin:	n/a	n/a
48	CTCF	chr15:45402500-45402650	GM12865	blood:	n/a	n/a
49	CTCF	chr15:45402500-45402650	AG09319	gingival:	n/a	n/a
50	CTCF	chr15:45402560-45402710	RPTEC	kidney:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:45405370-45405420	A549	lung:	n/a
2	chr15:45405370-45405420	A549	lung:	n/a
3	chr15:45404896-45404946	HL-60	blood:	n/a
4	chr15:45405167-45405217	AG04449	skin:	fetal
5	chr15:45405370-45405420	AoSMC	blood vessel:	n/a
6	chr15:45405167-45405217	AG09309	skin:	n/a
7	chr15:45404157-45404207	LNCaP	prostate:	n/a
8	chr15:45403733-45403783	SK-N-MC	brain:	n/a
9	chr15:45405167-45405217	Hela-S3	cervix:	n/a
10	chr15:45403733-45403783	K562	blood:	n/a
11	chr15:45405103-45405153	HMEC	breast:	n/a
12	chr15:45405167-45405217	MCF10A-Er-Src	breast:	n/a
13	chr15:45405103-45405153	AoSMC	blood vessel:	n/a
14	chr15:45405167-45405217	U87	brain:	n/a
15	chr15:45404896-45404946	RPTEC	kidney:	n/a
16	chr15:45404896-45404946	U87	brain:	n/a
17	chr15:45404157-45404207	T-47D	breast:	n/a
18	chr15:45404896-45404946	SAEC	small airway:	n/a
19	chr15:45403733-45403783	Caco-2	colon:	n/a
20	chr15:45403733-45403783	HCM	heart:	n/a
21	chr15:45404896-45404946	HepG2	liver:	n/a
22	chr15:45405370-45405420	MCF-7	breast:	n/a
23	chr15:45404157-45404207	AG09309	skin:	n/a
24	chr15:45405103-45405153	GM06990	blood:	n/a
25	chr15:45405370-45405420	SK-N-MC	brain:	n/a
26	chr15:45405103-45405153	PrEC	prostate:	n/a
27	chr15:45404157-45404207	HEK293	kidney:	embryo
28	chr15:45405167-45405217	H1-hESC	embryonic stem cell:	embryo
29	chr15:45404157-45404207	HL-60	blood:	n/a
30	chr15:45403733-45403783	HIPEpiC	eye:	n/a
31	chr15:45405370-45405420	BJ	skin:	n/a
32	chr15:45403733-45403783	SK-N-SH	brain:	n/a
33	chr15:45404157-45404207	NT2-D1	testis:	n/a
34	chr15:45404896-45404946	H1-hESC	embryonic stem cell:	embryo
35	chr15:45404157-45404207	BE2_C	brain:	n/a
36	chr15:45405103-45405153	IMR90	lung:	fetal
37	chr15:45405370-45405420	AG09319	gingival:	n/a
38	chr15:45404896-45404946	Hepatocyte	liver:	n/a
39	chr15:45403733-45403783	GM19239	blood:	n/a
40	chr15:45405370-45405420	NH-A	brain:	n/a
41	chr15:45404157-45404207	NH-A	brain:	n/a
42	chr15:45405103-45405153	HNPCEpiC	eye:	n/a
43	chr15:45404896-45404946	NB4	blood:	n/a
44	chr15:45403733-45403783	HEK293	kidney:	embryo
45	chr15:45403733-45403783	ProgFib	skin:	n/a
46	chr15:45404896-45404946	LNCaP	prostate:	n/a
47	chr15:45405370-45405420	LNCaP	prostate:	n/a
48	chr15:45405103-45405153	T-47D	breast:	n/a
49	chr15:45405370-45405420	GM12878	blood:	n/a
50	chr15:45403733-45403783	HPAEpiC	pulmonary alveolar:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:45402965..45405384-chr15:45407818..45410560,2	K562	blood:
2	chr15:45380073..45381960-chr15:45400521..45403354,2	K562	blood:
3	chr15:45402172..45404057-chr15:45407808..45410481,2	MCF-7	breast:

No data

Variant related genes	Relation type
DUOXA2	TF binding region
DUOXA2	CpG island

Extended variants
information (count: 182 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:182 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191828816	chr15:45402406-45402407	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs551788567	chr15:45402415-45402416	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs72724247	chr15:45402429-45402430	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs553745707	chr15:45402438-45402439	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs571969751	chr15:45402469-45402470	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs113324656	chr15:45402479-45402480	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs376092886	chr15:45402501-45402502	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs111708176	chr15:45402506-45402507	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs568023150	chr15:45402526-45402527	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs374084745	chr15:45402556-45402557	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs536890454	chr15:45402585-45402586	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs368195994	chr15:45402590-45402591	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs374919001	chr15:45402600-45402601	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs370752559	chr15:45402626-45402627	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs375264413	chr15:45402629-45402630	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs573609412	chr15:45402630-45402631	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs367829065	chr15:45402639-45402640	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs201416182	chr15:45402679-45402680	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs559264063	chr15:45402685-45402686	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs370110153	chr15:45402688-45402689	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs377608586	chr15:45402692-45402693	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs148754510	chr15:45402701-45402702	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs544236153	chr15:45402707-45402708	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs368909888	chr15:45402709-45402710	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs555083063	chr15:45402713-45402714	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs142354994	chr15:45402716-45402717	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs372682461	chr15:45402735-45402736	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs377197782	chr15:45402737-45402738	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs540065615	chr15:45402748-45402749	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs369596611	chr15:45402759-45402760	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs372260934	chr15:45402805-45402806	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs201507902	chr15:45402816-45402817	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs370995201	chr15:45402821-45402822	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs79467028	chr15:45402830-45402831	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs373155740	chr15:45402836-45402837	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs545715198	chr15:45402838-45402839	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs562595411	chr15:45402850-45402851	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs376129290	chr15:45402859-45402860	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs200479757	chr15:45402880-45402881	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs151261408	chr15:45402883-45402884	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs568196384	chr15:45402888-45402889	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs140455650	chr15:45402893-45402894	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs527361236	chr15:45402898-45402899	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs144183694	chr15:45402903-45402904	Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs368847158	chr15:45402921-45402922	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567090708	chr15:45402927-45402928	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs269859	chr15:45402940-45402941	Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs386783603	chr15:45402951-45402952	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201947197	chr15:45402953-45402954	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148954300	chr15:45402957-45402958	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Melanoma	17363583	CNVD
Acute myeloid leukemia	19651601	CNVD
Marfan syndrome	17492313	CNVD
Esophageal adenocarcinoma	18820669	CNVD

Chromatin state (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45381400-45404600	Weak transcription	Right Atrium	heart
2	chr15:45402200-45402800	Enhancers	Gastric	stomach
3	chr15:45402400-45403200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:45402600-45402800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
5	chr15:45402600-45402800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
6	chr15:45402600-45402800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
7	chr15:45402800-45403000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
8	chr15:45402800-45403000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
9	chr15:45402800-45403800	Weak transcription	Gastric	stomach
10	chr15:45403600-45403800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr15:45403600-45404000	Enhancers	Lung	lung
12	chr15:45403600-45404200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr15:45403600-45404200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr15:45403600-45404600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
15	chr15:45403600-45404600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr15:45403600-45404600	Bivalent Enhancer	Right Ventricle	heart
17	chr15:45403800-45404000	Enhancers	Gastric	stomach
18	chr15:45403800-45404200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
19	chr15:45403800-45404200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr15:45403800-45404200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr15:45403800-45404400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr15:45403800-45404600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
23	chr15:45403800-45404600	Bivalent Enhancer	Primary B cells from cord blood	blood
24	chr15:45403800-45404600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
25	chr15:45403800-45404600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
26	chr15:45403800-45404600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr15:45403800-45404600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr15:45403800-45404600	Bivalent Enhancer	Fetal Heart	heart
29	chr15:45403800-45406800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
30	chr15:45403800-45407000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
31	chr15:45403800-45407000	Enhancers	Pancreas	Pancrea
32	chr15:45404000-45404200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
33	chr15:45404000-45404200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
34	chr15:45404000-45404200	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr15:45404000-45404200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
36	chr15:45404000-45404200	Flanking Bivalent TSS/Enh	Esophagus	oesophagus
37	chr15:45404000-45404200	Flanking Active TSS	Gastric	stomach
38	chr15:45404000-45404200	Bivalent Enhancer	Left Ventricle	heart
39	chr15:45404000-45404200	Bivalent Enhancer	Thymus	Thymus
40	chr15:45404000-45404400	Bivalent Enhancer	Brain Hippocampus Middle	brain
41	chr15:45404000-45404400	Bivalent Enhancer	Psoas Muscle	Psoas
42	chr15:45404000-45404400	Bivalent Enhancer	HMEC	breast
43	chr15:45404000-45404600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
44	chr15:45404000-45404600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
45	chr15:45404000-45404600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
46	chr15:45404000-45404600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr15:45404000-45404600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr15:45404000-45404600	Bivalent Enhancer	Brain Anterior Caudate	brain
49	chr15:45404000-45404600	Bivalent/Poised TSS	Colonic Mucosa	Colon
50	chr15:45404000-45404600	Bivalent Enhancer	Ovary	ovary

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