Variant report

Variant	esv3328504
Chromosome Location	chr15:55879460-55881833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:211)
CpG islands
(count:978)
Chromatin interactive
region (count:0)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:211 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr15:55879929-55880216	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr15:55880445-55881363	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr15:55879867-55879946	K562	blood:	n/a	n/a
4	CEBPB	chr15:55880784-55881050	A549	lung:	n/a	n/a
5	CEBPB	chr15:55880848-55880961	HepG2	liver:	n/a	n/a
6	CEBPB	chr15:55880741-55881105	IMR90	lung:	n/a	n/a
7	CHD1	chr15:55879925-55880096	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr15:55879678-55880854	A549	lung:	n/a	n/a
9	CTCF	chr15:55880480-55880630	HA-sp	spinal cord:	n/a	n/a
10	CTCF	chr15:55880400-55880550	AoAF	blood vessel:	n/a	n/a
11	CTCF	chr15:55880380-55880530	HPF	lung:	n/a	n/a
12	CTCF	chr15:55880440-55880590	HepG2	liver:	n/a	n/a
13	CTCF	chr15:55880452-55880530	MCF-7	breast:	n/a	n/a
14	CTCF	chr15:55880460-55880610	SAEC	small airway:	n/a	n/a
15	CTCF	chr15:55880442-55880562	GM13977	blood:	n/a	n/a
16	CTCF	chr15:55879800-55879950	AG04449	skin:	n/a	n/a
17	CTCF	chr15:55880476-55880540	ProgFib	skin:	n/a	n/a
18	CTCF	chr15:55880453-55880537	MCF-7	breast:	n/a	n/a
19	CTCF	chr15:55880410-55880555	MCF-7	breast:	n/a	n/a
20	CTCF	chr15:55880420-55880570	HMEC	breast:	n/a	n/a
21	CTCF	chr15:55880400-55880550	AG04449	skin:	n/a	n/a
22	CTCF	chr15:55880400-55880550	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr15:55880420-55880570	Caco-2	colon:	n/a	n/a
24	CTCF	chr15:55880860-55881010	A549	lung:	n/a	n/a
25	CTCF	chr15:55880420-55880570	NB4	blood:	n/a	n/a
26	CTCF	chr15:55880450-55880520	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr15:55880400-55880550	HMF	breast:	n/a	n/a
28	CTCF	chr15:55880466-55880531	Lung_OC	lung:	n/a	n/a
29	CTCF	chr15:55880387-55880534	LNCaP	prostate:	n/a	n/a
30	CTCF	chr15:55880420-55880570	BE2_C	brain:	n/a	n/a
31	CTCF	chr15:55880400-55880550	RPTEC	kidney:	n/a	n/a
32	CTCF	chr15:55880420-55880570	HCFaa	heart:	n/a	n/a
33	CTCF	chr15:55880450-55880535	MCF-7	breast:	n/a	n/a
34	CTCF	chr15:55880454-55880521	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr15:55880433-55880536	GM19238	blood:	n/a	n/a
36	CTCF	chr15:55880380-55880530	HRE	kidney:	n/a	n/a
37	CTCF	chr15:55880400-55880550	GM12875	blood:	n/a	n/a
38	CTCF	chr15:55880360-55880510	GM06990	blood:	n/a	n/a
39	CTCF	chr15:55880360-55880510	AG09319	gingival:	n/a	n/a
40	CTCF	chr15:55880400-55880550	AG04450	lung:	n/a	n/a
41	CTCF	chr15:55880400-55880550	Caco-2	colon:	n/a	n/a
42	CTCF	chr15:55880427-55880563	A549	lung:	n/a	n/a
43	CTCF	chr15:55880469-55880499	GM12878	blood:	n/a	n/a
44	CTCF	chr15:55880400-55880550	HCM	heart:	n/a	n/a
45	CTCF	chr15:55880400-55880547	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr15:55880380-55880530	AG04449	skin:	n/a	n/a
47	CTCF	chr15:55880460-55880610	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr15:55880420-55880570	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr15:55880860-55881010	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr15:55880400-55880550	GM12871	blood:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:55881607-55881657	PrEC	prostate:	n/a
2	chr15:55881089-55881139	Hepatocyte	liver:	n/a
3	chr15:55881607-55881657	PrEC	prostate:	n/a
4	chr15:55881089-55881139	Hepatocyte	liver:	n/a
5	chr15:55881083-55881133	Jurkat	blood:	n/a
6	chr15:55879749-55879799	T-47D	breast:	n/a
7	chr15:55880470-55880520	GM06990	blood:	n/a
8	chr15:55881081-55881131	CMK	blood:	n/a
9	chr15:55880894-55880944	NB4	blood:	n/a
10	chr15:55881075-55881125	NHBE	bronchial:	n/a
11	chr15:55881044-55881094	AG09309	skin:	n/a
12	chr15:55881599-55881649	MCF-7	breast:	n/a
13	chr15:55881083-55881133	HNPCEpiC	eye:	n/a
14	chr15:55880470-55880520	PFSK-1	brain:	n/a
15	chr15:55880470-55880520	NT2-D1	testis:	n/a
16	chr15:55881607-55881657	HAEpiC	amniotic membrane:	n/a
17	chr15:55880470-55880520	K562	blood:	n/a
18	chr15:55881083-55881133	IMR90	lung:	fetal
19	chr15:55881089-55881139	Jurkat	blood:	n/a
20	chr15:55881089-55881139	AG04449	skin:	fetal
21	chr15:55879749-55879799	NB4	blood:	n/a
22	chr15:55880224-55880274	A549	lung:	n/a
23	chr15:55881599-55881649	CMK	blood:	n/a
24	chr15:55880224-55880274	HepG2	liver:	n/a
25	chr15:55880224-55880274	NHBE	bronchial:	n/a
26	chr15:55879749-55879799	HCT-116	colon:	n/a
27	chr15:55881599-55881649	HCF	heart:	n/a
28	chr15:55881599-55881649	HCPEpiC	choroid plexus:	n/a
29	chr15:55880470-55880520	NHDF-neo	bronchial:	n/a
30	chr15:55880470-55880520	GM19239	blood:	n/a
31	chr15:55881083-55881133	HEEpiC	esophagus:	n/a
32	chr15:55881083-55881133	HEK293	kidney:	embryo
33	chr15:55881089-55881139	AG04450	lung:	fetal
34	chr15:55881044-55881094	T-47D	breast:	n/a
35	chr15:55881162-55881212	ECC-1	luminal epithelium:	n/a
36	chr15:55881607-55881657	HUVEC	blood vessel:	n/a
37	chr15:55881607-55881657	SAEC	small airway:	n/a
38	chr15:55880894-55880944	BJ	skin:	n/a
39	chr15:55880894-55880944	SAEC	small airway:	n/a
40	chr15:55881706-55881756	HAEpiC	amniotic membrane:	n/a
41	chr15:55880894-55880944	Caco-2	colon:	n/a
42	chr15:55881044-55881094	PrEC	prostate:	n/a
43	chr15:55881044-55881094	HEK293	kidney:	embryo
44	chr15:55880894-55880944	Jurkat	blood:	n/a
45	chr15:55881089-55881139	Caco-2	colon:	n/a
46	chr15:55880894-55880944	MCF10A-Er-Src	breast:	n/a
47	chr15:55881081-55881131	AG10803	skin:	n/a
48	chr15:55880224-55880274	T-47D	breast:	n/a
49	chr15:55880470-55880520	HCM	heart:	n/a
50	chr15:55881083-55881133	HCM	heart:	n/a

No data

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-178D12.1.1-5	chr15:55881501-55882082	NONHSAT044003
2	lnc-RP11-178D12.1.1-5	chr15:55880889-55881017	NONHSAT044003

No data

Variant related genes	Relation type
PYGO1	TF binding region
PYGO1	CpG island

Extended variants
information (count: 92 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143056391	chr15:55879468-55879469	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs374199952	chr15:55879512-55879513	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188629290	chr15:55879516-55879517	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573036386	chr15:55879533-55879534	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541620085	chr15:55879536-55879537	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117957700	chr15:55879555-55879556	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs493480	chr15:55879574-55879575	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550633807	chr15:55879576-55879577	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564097090	chr15:55879582-55879583	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192297308	chr15:55879589-55879590	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369039444	chr15:55879603-55879604	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs62021897	chr15:55879675-55879676	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs547358004	chr15:55879678-55879679	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs4561397	chr15:55879679-55879680	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs560585134	chr15:55879681-55879682	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs536047316	chr15:55879685-55879686	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs549281814	chr15:55879687-55879688	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs76453161	chr15:55879712-55879713	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs535114866	chr15:55879727-55879728	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs140263995	chr15:55879737-55879738	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs549238577	chr15:55879738-55879739	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs557810536	chr15:55879758-55879759	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs184356240	chr15:55879769-55879770	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs150346238	chr15:55879774-55879775	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs544547254	chr15:55879829-55879830	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs138056158	chr15:55879831-55879832	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs573006473	chr15:55879850-55879851	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs560434649	chr15:55879854-55879855	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs542031355	chr15:55879860-55879861	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs555237819	chr15:55879939-55879940	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs575373193	chr15:55879969-55879970	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs544367427	chr15:55880001-55880002	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs186862237	chr15:55880011-55880012	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs75131234	chr15:55880106-55880107	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs202218683	chr15:55880107-55880108	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs540186565	chr15:55880109-55880110	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs560859252	chr15:55880220-55880221	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs184350361	chr15:55880319-55880320	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs529525511	chr15:55880350-55880351	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs542038034	chr15:55880381-55880382	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs370925158	chr15:55880382-55880383	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs527489864	chr15:55880384-55880385	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs535134728	chr15:55880412-55880413	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs569380413	chr15:55880468-55880469	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs531931211	chr15:55880536-55880537	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs551504171	chr15:55880589-55880590	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs565903480	chr15:55880786-55880787	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs35576348	chr15:55880787-55880788	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs373959639	chr15:55880824-55880825	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs571369887	chr15:55880879-55880880	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD

Chromatin state (count:337 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55877400-55881600	Active TSS	Skeletal Muscle Female	skeletal muscle
2	chr15:55878000-55879800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr15:55878200-55879800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr15:55878200-55879800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr15:55878200-55879800	Flanking Active TSS	Fetal Brain Male	brain
6	chr15:55878400-55879800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:55878400-55880200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
8	chr15:55878400-55881600	Active TSS	Stomach Smooth Muscle	stomach
9	chr15:55878400-55881800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
10	chr15:55878600-55879600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
11	chr15:55878800-55879600	Flanking Active TSS	Fetal Lung	lung
12	chr15:55878800-55880000	Flanking Active TSS	HUVEC	blood vessel
13	chr15:55878800-55881400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
14	chr15:55878800-55881600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
15	chr15:55878800-55881600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr15:55878800-55881800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr15:55879000-55879600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr15:55879000-55879600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
19	chr15:55879000-55879600	Bivalent/Poised TSS	Fetal Intestine Small	intestine
20	chr15:55879000-55879600	Active TSS	Rectal Smooth Muscle	rectum
21	chr15:55879000-55881000	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
22	chr15:55879000-55881200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr15:55879000-55881400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr15:55879000-55881400	Active TSS	Psoas Muscle	Psoas
25	chr15:55879000-55881600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr15:55879000-55881600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
27	chr15:55879000-55881600	Active TSS	Ovary	ovary
28	chr15:55879000-55881600	Active TSS	HSMM	muscle
29	chr15:55879200-55879600	Flanking Active TSS	Fetal Brain Female	brain
30	chr15:55879200-55879600	Flanking Active TSS	Fetal Heart	heart
31	chr15:55879200-55881000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr15:55879200-55881000	Bivalent/Poised TSS	Fetal Intestine Large	intestine
33	chr15:55879200-55881000	Active TSS	Fetal Muscle Leg	muscle
34	chr15:55879200-55881200	Active TSS	Muscle Satellite Cultured Cells	--
35	chr15:55879200-55881200	Active TSS	A549	lung
36	chr15:55879200-55881400	Active TSS	Fetal Stomach	stomach
37	chr15:55879200-55881400	Active TSS	NHLF	lung
38	chr15:55879200-55881600	Active TSS	NH-A	brain
39	chr15:55879200-55881800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr15:55879200-55881800	Active TSS	NHDF-Ad	bronchial
41	chr15:55879400-55879600	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
42	chr15:55879400-55879600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr15:55879400-55879600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr15:55879400-55879600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
45	chr15:55879400-55879600	Bivalent Enhancer	Brain Angular Gyrus	brain
46	chr15:55879400-55879600	Active TSS	Fetal Muscle Trunk	muscle
47	chr15:55879400-55879600	Weak transcription	Placenta	Placenta
48	chr15:55879400-55879600	Active TSS	HSMMtube	muscle
49	chr15:55879400-55879800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
50	chr15:55879400-55879800	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood

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