Variant report

Variant	esv3373041
Chromosome Location	chr15:55878885-55882033
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:976)
Chromatin interactive
region (count:3)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 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	chr15:55880380-55880530	HPF	lung:	n/a	n/a
10	CTCF	chr15:55880440-55880590	HAc	cerebellar:	n/a	n/a
11	CTCF	chr15:55880380-55880530	HRE	kidney:	n/a	n/a
12	CTCF	chr15:55880469-55880499	GM12878	blood:	n/a	n/a
13	CTCF	chr15:55880420-55880570	HCFaa	heart:	n/a	n/a
14	CTCF	chr15:55880440-55880590	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr15:55880460-55880610	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr15:55880425-55880585	Fibrobl	skin:	n/a	n/a
17	CTCF	chr15:55880387-55880534	LNCaP	prostate:	n/a	n/a
18	CTCF	chr15:55880420-55880570	BE2_C	brain:	n/a	n/a
19	CTCF	chr15:55880476-55880540	ProgFib	skin:	n/a	n/a
20	CTCF	chr15:55880453-55880537	MCF-7	breast:	n/a	n/a
21	CTCF	chr15:55880450-55880535	MCF-7	breast:	n/a	n/a
22	CTCF	chr15:55880438-55880533	NHEK	skin:	n/a	n/a
23	CTCF	chr15:55880040-55880190	AG04449	skin:	n/a	n/a
24	CTCF	chr15:55880420-55880570	HMEC	breast:	n/a	n/a
25	CTCF	chr15:55880420-55880570	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr15:55880460-55880610	SAEC	small airway:	n/a	n/a
27	CTCF	chr15:55880360-55880510	BJ	skin:	n/a	n/a
28	CTCF	chr15:55880420-55880570	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr15:55880466-55880531	Lung_OC	lung:	n/a	n/a
30	CTCF	chr15:55880420-55880570	Caco-2	colon:	n/a	n/a
31	CTCF	chr15:55880432-55880544	GM12891	blood:	n/a	n/a
32	CTCF	chr15:55880360-55880510	AG09319	gingival:	n/a	n/a
33	CTCF	chr15:55880440-55880674	IMR90	lung:	n/a	n/a
34	CTCF	chr15:55880400-55880550	AG04449	skin:	n/a	n/a
35	CTCF	chr15:55880400-55880550	GM12871	blood:	n/a	n/a
36	CTCF	chr15:55880410-55880555	MCF-7	breast:	n/a	n/a
37	CTCF	chr15:55880360-55880510	GM06990	blood:	n/a	n/a
38	CTCF	chr15:55880380-55880530	AG04449	skin:	n/a	n/a
39	CTCF	chr15:55880880-55881030	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr15:55880400-55880550	GM12875	blood:	n/a	n/a
41	CTCF	chr15:55880454-55880521	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr15:55880480-55880630	GM12864	blood:	n/a	n/a
43	CTCF	chr15:55880460-55880610	GM12869	blood:	n/a	n/a
44	CTCF	chr15:55880400-55880550	HMF	breast:	n/a	n/a
45	CTCF	chr15:55880440-55880590	HepG2	liver:	n/a	n/a
46	CTCF	chr15:55880450-55880520	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr15:55880400-55880547	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr15:55880400-55880550	Caco-2	colon:	n/a	n/a
49	CTCF	chr15:55880442-55880562	GM13977	blood:	n/a	n/a
50	CTCF	chr15:55880860-55881010	HBMEC	blood vessel:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:55881162-55881212	CMK	blood:	n/a
2	chr15:55881089-55881139	U87	brain:	n/a
3	chr15:55881075-55881125	Caco-2	colon:	n/a
4	chr15:55881607-55881657	AG04449	skin:	fetal
5	chr15:55881246-55881296	IMR90	lung:	fetal
6	chr15:55881044-55881094	HNPCEpiC	eye:	n/a
7	chr15:55881706-55881756	GM19239	blood:	n/a
8	chr15:55881081-55881131	IMR90	lung:	fetal
9	chr15:55881044-55881094	T-47D	breast:	n/a
10	chr15:55880224-55880274	HRCEpiC	kidney:	n/a
11	chr15:55880089-55880139	RPTEC	kidney:	n/a
12	chr15:55881607-55881657	NT2-D1	testis:	n/a
13	chr15:55880089-55880139	A549	lung:	n/a
14	chr15:55881075-55881125	ProgFib	skin:	n/a
15	chr15:55881083-55881133	SAEC	small airway:	n/a
16	chr15:55881083-55881133	BE2_C	brain:	n/a
17	chr15:55879749-55879799	AG04450	lung:	fetal
18	chr15:55881246-55881296	AG04449	skin:	fetal
19	chr15:55881083-55881133	GM12891	blood:	n/a
20	chr15:55881089-55881139	HEEpiC	esophagus:	n/a
21	chr15:55881246-55881296	AG10803	skin:	n/a
22	chr15:55881599-55881649	HCM	heart:	n/a
23	chr15:55880224-55880274	LNCaP	prostate:	n/a
24	chr15:55879749-55879799	NHDF-neo	bronchial:	n/a
25	chr15:55880224-55880274	HRPEpiC	eye:	n/a
26	chr15:55880470-55880520	RPTEC	kidney:	n/a
27	chr15:55881081-55881131	HAEpiC	amniotic membrane:	n/a
28	chr15:55881075-55881125	ovcar-3	ovarian:	n/a
29	chr15:55881607-55881657	LNCaP	prostate:	n/a
30	chr15:55881075-55881125	SK-N-SH_RA	brain:	n/a
31	chr15:55881162-55881212	SK-N-SH	brain:	n/a
32	chr15:55881246-55881296	GM12878	blood:	n/a
33	chr15:55881706-55881756	AG04450	lung:	fetal
34	chr15:55881075-55881125	K562	blood:	n/a
35	chr15:55881044-55881094	PrEC	prostate:	n/a
36	chr15:55881607-55881657	SK-N-MC	brain:	n/a
37	chr15:55881083-55881133	BJ	skin:	n/a
38	chr15:55879749-55879799	SK-N-SH_RA	brain:	n/a
39	chr15:55881089-55881139	NHBE	bronchial:	n/a
40	chr15:55881246-55881296	HRE	kidney:	n/a
41	chr15:55881246-55881296	H1-hESC	embryonic stem cell:	embryo
42	chr15:55880894-55880944	NHBE	bronchial:	n/a
43	chr15:55881075-55881125	Jurkat	blood:	n/a
44	chr15:55881089-55881139	BE2_C	brain:	n/a
45	chr15:55879749-55879799	RPTEC	kidney:	n/a
46	chr15:55881246-55881296	CMK	blood:	n/a
47	chr15:55881089-55881139	A549	lung:	n/a
48	chr15:55881044-55881094	HCM	heart:	n/a
49	chr15:55881083-55881133	AG09309	skin:	n/a
50	chr15:55880470-55880520	HNPCEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:55881922..55884171-chr15:55889698..55891738,2	MCF-7	breast:
2	chr15:55875375..55879008-chr15:55880167..55883388,4	K562	blood:
3	chr15:55876611..55879059-chr15:55880096..55882468,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
PYGO1	TF binding region
PYGO1	CpG island
ENSG00000171016	chromatin interactions

Extended variants
information (count: 122 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:122 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555574730	chr15:55878916-55878917	Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs575632479	chr15:55878917-55878918	Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs193229350	chr15:55878924-55878925	Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs142614342	chr15:55878972-55878973	Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs537346501	chr15:55878973-55878974	Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs550953801	chr15:55878983-55878984	Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532243353	chr15:55879031-55879032	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs144970377	chr15:55879039-55879040	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs114167012	chr15:55879094-55879095	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs62021895	chr15:55879100-55879101	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570794777	chr15:55879122-55879123	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147559259	chr15:55879140-55879141	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548314709	chr15:55879150-55879151	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114706525	chr15:55879156-55879157	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545235	chr15:55879182-55879183	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571184300	chr15:55879210-55879211	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs79908179	chr15:55879239-55879240	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547291879	chr15:55879241-55879242	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566042830	chr15:55879293-55879294	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184046447	chr15:55879316-55879317	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567115503	chr15:55879326-55879327	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535661426	chr15:55879385-55879386	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555837683	chr15:55879388-55879389	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141965885	chr15:55879401-55879402	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538258221	chr15:55879406-55879407	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557694078	chr15:55879449-55879450	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs62021896	chr15:55879453-55879454	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	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
36	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
37	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
38	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
39	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
40	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
41	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
42	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
43	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
44	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
45	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
46	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
47	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
48	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
49	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
50	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

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:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55858000-55879400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:55865600-55879000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr15:55876600-55879400	Weak transcription	Fetal Muscle Trunk	muscle
4	chr15:55877400-55881600	Active TSS	Skeletal Muscle Female	skeletal muscle
5	chr15:55877600-55879000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr15:55877600-55879200	Active TSS	Fetal Brain Female	brain
7	chr15:55877800-55879400	Flanking Active TSS	Brain Germinal Matrix	brain
8	chr15:55878000-55879800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr15:55878200-55879000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr15:55878200-55879000	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
11	chr15:55878200-55879200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr15:55878200-55879400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr15:55878200-55879800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr15:55878200-55879800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr15:55878200-55879800	Flanking Active TSS	Fetal Brain Male	brain
16	chr15:55878400-55879200	Enhancers	Fetal Muscle Leg	muscle
17	chr15:55878400-55879400	Flanking Active TSS	Colon Smooth Muscle	Colon
18	chr15:55878400-55879800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr15:55878400-55880200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
20	chr15:55878400-55881600	Active TSS	Stomach Smooth Muscle	stomach
21	chr15:55878400-55881800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
22	chr15:55878600-55879000	Enhancers	Fetal Stomach	stomach
23	chr15:55878600-55879400	Enhancers	Adipose Nuclei	Adipose
24	chr15:55878600-55879600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
25	chr15:55878800-55879000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr15:55878800-55879000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr15:55878800-55879000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr15:55878800-55879000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
29	chr15:55878800-55879000	Bivalent/Poised TSS	Brain Angular Gyrus	brain
30	chr15:55878800-55879000	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
31	chr15:55878800-55879000	Flanking Active TSS	Ovary	ovary
32	chr15:55878800-55879000	Enhancers	Placenta Amnion	Placenta Amnion
33	chr15:55878800-55879000	Flanking Active TSS	Psoas Muscle	Psoas
34	chr15:55878800-55879000	Flanking Active TSS	Rectal Smooth Muscle	rectum
35	chr15:55878800-55879000	Enhancers	HepG2	liver
36	chr15:55878800-55879000	Enhancers	HSMM	muscle
37	chr15:55878800-55879200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
38	chr15:55878800-55879200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr15:55878800-55879200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr15:55878800-55879200	Enhancers	Fetal Heart	heart
41	chr15:55878800-55879200	Flanking Active TSS	A549	lung
42	chr15:55878800-55879200	Active TSS	HSMMtube	muscle
43	chr15:55878800-55879200	Flanking Active TSS	NH-A	brain
44	chr15:55878800-55879200	Flanking Active TSS	NHDF-Ad	bronchial
45	chr15:55878800-55879200	Flanking Active TSS	NHLF	lung
46	chr15:55878800-55879400	Flanking Active TSS	Fetal Kidney	kidney
47	chr15:55878800-55879400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
48	chr15:55878800-55879400	Flanking Active TSS	Osteobl	bone
49	chr15:55878800-55879600	Flanking Active TSS	Fetal Lung	lung
50	chr15:55878800-55880000	Flanking Active TSS	HUVEC	blood vessel

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