Variant report

Variant	nsv457158
Chromosome Location	chr15:55930542-55982257
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:55933805-55934122	K562	blood:	n/a	n/a
2	ARID3A	chr15:55933818-55934139	HepG2	liver:	n/a	n/a
3	ATF1	chr15:55939036-55939172	K562	blood:	n/a	n/a
4	ATF2	chr15:55977465-55977883	GM12878	blood:	n/a	n/a
5	ATF2	chr15:55977363-55977942	GM12878	blood:	n/a	n/a
6	BATF	chr15:55977485-55977821	GM12878	blood:	n/a	n/a
7	BATF	chr15:55977447-55977812	GM12878	blood:	n/a	n/a
8	BCL11A	chr15:55977469-55977811	GM12878	blood:	n/a	n/a
9	CEBPB	chr15:55977590-55977850	A549	lung:	n/a	n/a
10	CEBPB	chr15:55953571-55954128	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr15:55940570-55940965	A549	lung:	n/a	chr15:55940664-55940677
12	CEBPB	chr15:55977598-55977858	HepG2	liver:	n/a	n/a
13	CEBPB	chr15:55968646-55968895	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr15:55973198-55973342	K562	blood:	n/a	n/a
15	CEBPB	chr15:55954982-55955106	A549	lung:	n/a	n/a
16	CEBPB	chr15:55977545-55977851	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr15:55973161-55973308	A549	lung:	n/a	n/a
18	CEBPB	chr15:55974418-55974462	HepG2	liver:	n/a	chr15:55974432-55974444
19	CEBPB	chr15:55930437-55930649	K562	blood:	n/a	chr15:55930538-55930549 chr15:55930536-55930549
20	CEBPB	chr15:55970432-55970614	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr15:55954070-55954128	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr15:55970112-55970142	HepG2	liver:	n/a	n/a
23	CTCF	chr15:55933907-55934085	Lung_OC	lung:	n/a	chr15:55933994-55934010 chr15:55933995-55934008 chr15:55933988-55934009 chr15:55933993-55934011
24	CTCF	chr15:55933920-55934070	HAc	cerebellar:	n/a	chr15:55933994-55934010 chr15:55933995-55934008 chr15:55933988-55934009 chr15:55933993-55934011
25	CTCF	chr15:55940660-55940810	HEK293	kidney:	n/a	chr15:55940747-55940755 chr15:55940743-55940759 chr15:55940744-55940765
26	CTCF	chr15:55940680-55940830	GM12872	blood:	n/a	chr15:55940747-55940755 chr15:55940743-55940759 chr15:55940744-55940765
27	CTCF	chr15:55940680-55940830	AG04449	skin:	n/a	chr15:55940747-55940755 chr15:55940743-55940759 chr15:55940744-55940765
28	CTCF	chr15:55940559-55940995	A549	lung:	n/a	chr15:55940747-55940755 chr15:55940743-55940759 chr15:55940744-55940765
29	CTCF	chr15:55933763-55934177	IMR90	lung:	n/a	chr15:55933994-55934010 chr15:55933995-55934008 chr15:55933988-55934009 chr15:55933993-55934011
30	CTCF	chr15:55940512-55940945	MCF-7	breast:	n/a	chr15:55940747-55940755 chr15:55940743-55940759 chr15:55940744-55940765
31	CTCF	chr15:55933940-55934090	HMEC	breast:	n/a	chr15:55933994-55934010 chr15:55933995-55934008 chr15:55933988-55934009 chr15:55933993-55934011
32	CTCF	chr15:55940660-55940810	GM12868	blood:	n/a	chr15:55940747-55940755 chr15:55940743-55940759 chr15:55940744-55940765
33	CTCF	chr15:55933748-55934168	A549	lung:	n/a	chr15:55933994-55934010 chr15:55933995-55934008 chr15:55933988-55934009 chr15:55933993-55934011
34	CTCF	chr15:55933911-55934078	HepG2	liver:	n/a	chr15:55933994-55934010 chr15:55933995-55934008 chr15:55933988-55934009 chr15:55933993-55934011
35	CTCF	chr15:55940434-55940993	MCF-7	breast:	n/a	chr15:55940747-55940755 chr15:55940743-55940759 chr15:55940744-55940765
36	CTCF	chr15:55940720-55940870	K562	blood:	n/a	chr15:55940747-55940755 chr15:55940743-55940759 chr15:55940744-55940765
37	CTCF	chr15:55940700-55940850	RPTEC	kidney:	n/a	chr15:55940747-55940755 chr15:55940743-55940759 chr15:55940744-55940765
38	CTCF	chr15:55933876-55934096	LNCaP	prostate:	n/a	chr15:55933994-55934010 chr15:55933995-55934008 chr15:55933988-55934009 chr15:55933993-55934011
39	CTCF	chr15:55933922-55934062	GM20000	blood:	n/a	chr15:55933994-55934010 chr15:55933995-55934008 chr15:55933988-55934009 chr15:55933993-55934011
40	CTCF	chr15:55933880-55934030	GM12874	blood:	n/a	chr15:55933994-55934010 chr15:55933995-55934008 chr15:55933988-55934009 chr15:55933993-55934011
41	CTCF	chr15:55933844-55934125	Medullo	brain:	n/a	chr15:55933994-55934010 chr15:55933995-55934008 chr15:55933988-55934009 chr15:55933993-55934011
42	CTCF	chr15:55933900-55934050	HRPEpiC	eye:	n/a	chr15:55933994-55934010 chr15:55933995-55934008 chr15:55933988-55934009 chr15:55933993-55934011
43	CTCF	chr15:55940644-55940857	MCF-7	breast:	n/a	chr15:55940747-55940755 chr15:55940743-55940759 chr15:55940744-55940765
44	CTCF	chr15:55940700-55940850	GM12864	blood:	n/a	chr15:55940747-55940755 chr15:55940743-55940759 chr15:55940744-55940765
45	CTCF	chr15:55940598-55940833	A549	lung:	n/a	chr15:55940747-55940755 chr15:55940743-55940759 chr15:55940744-55940765
46	CTCF	chr15:55940100-55940250	BJ	skin:	n/a	n/a
47	CTCF	chr15:55953447-55953471	Gliobla	brain:	n/a	n/a
48	CTCF	chr15:55933880-55934030	WI-38	lung:	n/a	chr15:55933994-55934010 chr15:55933995-55934008 chr15:55933988-55934009 chr15:55933993-55934011
49	CTCF	chr15:55940600-55940750	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr15:55940660-55940810	HVMF	connective:	n/a	chr15:55940747-55940755 chr15:55940743-55940759 chr15:55940744-55940765

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:55968870-55968920	AG04449	skin:	fetal
2	chr15:55968637-55968687	HCT-116	colon:	n/a
3	chr15:55944483-55944533	LNCaP	prostate:	n/a
4	chr15:55968870-55968920	HepG2	liver:	n/a
5	chr15:55968637-55968687	K562	blood:	n/a
6	chr15:55968870-55968920	GM12891	blood:	n/a
7	chr15:55944483-55944533	Hepatocyte	liver:	n/a
8	chr15:55968870-55968920	SKMC	muscle:	n/a
9	chr15:55944483-55944533	GM06990	blood:	n/a
10	chr15:55968637-55968687	SK-N-SH_RA	brain:	n/a
11	chr15:55968637-55968687	NHDF-neo	bronchial:	n/a
12	chr15:55944483-55944533	AG04449	skin:	fetal
13	chr15:55944483-55944533	ProgFib	skin:	n/a
14	chr15:55954199-55954249	GM06990	blood:	n/a
15	chr15:55968637-55968687	PFSK-1	brain:	n/a
16	chr15:55968637-55968687	HMEC	breast:	n/a
17	chr15:55968637-55968687	AoSMC	blood vessel:	n/a
18	chr15:55968870-55968920	AG09319	gingival:	n/a
19	chr15:55968870-55968920	AG09309	skin:	n/a
20	chr15:55968870-55968920	IMR90	lung:	fetal
21	chr15:55968637-55968687	GM12892	blood:	n/a
22	chr15:55968870-55968920	HUVEC	blood vessel:	n/a
23	chr15:55954199-55954249	HEK293	kidney:	embryo
24	chr15:55954199-55954249	PFSK-1	brain:	n/a
25	chr15:55968637-55968687	AG10803	skin:	n/a
26	chr15:55954199-55954249	NH-A	brain:	n/a
27	chr15:55954199-55954249	SK-N-SH	brain:	n/a
28	chr15:55968870-55968920	GM19239	blood:	n/a
29	chr15:55968637-55968687	Caco-2	colon:	n/a
30	chr15:55944483-55944533	GM12892	blood:	n/a
31	chr15:55944483-55944533	HEEpiC	esophagus:	n/a
32	chr15:55968870-55968920	GM06990	blood:	n/a
33	chr15:55968870-55968920	HRPEpiC	eye:	n/a
34	chr15:55968637-55968687	PANC-1	pancreas:	n/a
35	chr15:55954199-55954249	HIPEpiC	eye:	n/a
36	chr15:55954199-55954249	AG09309	skin:	n/a
37	chr15:55968870-55968920	LNCaP	prostate:	n/a
38	chr15:55944483-55944533	Hela-S3	cervix:	n/a
39	chr15:55954199-55954249	NT2-D1	testis:	n/a
40	chr15:55968870-55968920	HRE	kidney:	n/a
41	chr15:55944483-55944533	K562	blood:	n/a
42	chr15:55968637-55968687	NB4	blood:	n/a
43	chr15:55954199-55954249	Hepatocyte	liver:	n/a
44	chr15:55944483-55944533	SAEC	small airway:	n/a
45	chr15:55968637-55968687	HCM	heart:	n/a
46	chr15:55968870-55968920	HCM	heart:	n/a
47	chr15:55954199-55954249	NB4	blood:	n/a
48	chr15:55954199-55954249	HCF	heart:	n/a
49	chr15:55968637-55968687	GM19239	blood:	n/a
50	chr15:55954199-55954249	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:55955042..55958046-chr15:56034053..56035749,3	MCF-7	breast:
2	chr15:55957804..55959845-chr15:56026147..56028031,2	MCF-7	breast:
3	chr15:55940297..55941155-chr15:56138005..56138994,3	K562	blood:
4	chr15:55936558..55939197-chr15:55940435..55942868,2	K562	blood:
5	chr15:55948243..55950096-chr15:55952230..55953920,2	MCF-7	breast:
6	chr15:55818426..55819436-chr15:55933526..55934353,4	MCF-7	breast:
7	chr15:55940663..55943471-chr15:56092171..56094031,2	MCF-7	breast:
8	chr15:55940727..55941250-chr15:56344682..56345231,2	K562	blood:
9	chr15:55940251..55940793-chr15:56189676..56190326,2	K562	blood:
10	chr15:55805811..55806979-chr15:55933287..55934076,3	MCF-7	breast:
11	chr15:55940259..55941893-chr15:56091674..56092667,4	K562	blood:
12	chr15:55940303..55941439-chr15:56091892..56092613,4	MCF-7	breast:
13	chr15:55940282..55941119-chr15:56116751..56117288,2	MCF-7	breast:
14	chr15:55940286..55941226-chr15:56189659..56190472,2	MCF-7	breast:
15	chr15:55936558..55939197-chr15:55940435..55942868,2	K562	blood:
16	chr15:55940700..55941248-chr15:56066693..56067247,2	K562	blood:
17	chr15:55965960..55968011-chr15:56032220..56035162,2	MCF-7	breast:
18	chr15:55940442..55941185-chr15:56720975..56721740,2	K562	blood:
19	chr15:55948774..55951298-chr15:56033579..56035270,2	MCF-7	breast:
20	chr15:55808580..55811274-chr15:55928806..55931409,2	MCF-7	breast:
21	chr15:55940223..55941251-chr15:56138147..56138992,3	MCF-7	breast:
22	chr15:55938125..55940759-chr15:56034176..56036288,2	MCF-7	breast:
23	chr15:55956127..55957682-chr15:55978986..55980694,2	MCF-7	breast:
24	chr15:55945016..55946690-chr15:55947517..55950057,2	MCF-7	breast:
25	chr15:55951550..55954249-chr15:56034622..56036474,2	MCF-7	breast:
26	chr15:55959923..55962464-chr15:55970382..55973245,2	MCF-7	breast:
27	chr15:55963506..55965782-chr15:55969955..55972854,2	MCF-7	breast:
28	chr15:55939872..55941462-chr15:56091567..56092720,22	MCF-7	breast:
29	chr15:55936558..55938114-chr15:55939033..55941935,2	K562	blood:
30	chr15:55811685..55812599-chr15:55933611..55934492,2	MCF-7	breast:
31	chr15:55945016..55946690-chr15:55947517..55950057,2	MCF-7	breast:
32	chr15:55973838..55975695-chr15:56033955..56035878,2	MCF-7	breast:
33	chr15:55961153..55963651-chr15:56033694..56036455,3	MCF-7	breast:
34	chr15:55936558..55938114-chr15:55939033..55941935,2	K562	blood:
35	chr15:55818609..55819363-chr15:55933519..55934249,2	MCF-7	breast:
36	chr15:55948243..55950096-chr15:55952230..55953920,2	MCF-7	breast:
37	chr15:55956127..55957682-chr15:55978986..55980694,2	MCF-7	breast:
38	chr15:55940342..55940845-chr15:56538253..56538849,2	MCF-7	breast:

Variant related genes	Relation type
PRTG	TF binding region
ENSG00000259180	TF binding region
PRTG	CpG island
ENSG00000259180	CpG island
ENSG00000166450	chromatin interactions
ENSG00000259180	chromatin interactions

Extended variants
information (count: 1987 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1987 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs720509	chr15:55930542-55930543	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543632742	chr15:55930555-55930556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs489672	chr15:55930577-55930578	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs576915554	chr15:55930629-55930630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545838563	chr15:55930677-55930678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188801471	chr15:55930682-55930683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192682430	chr15:55930726-55930727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369121044	chr15:55930776-55930777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541283255	chr15:55930778-55930779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372875460	chr15:55930784-55930785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369525385	chr15:55930801-55930802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201846185	chr15:55930816-55930817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371188175	chr15:55930819-55930820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200941187	chr15:55930826-55930827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377409534	chr15:55930830-55930831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs61729647	chr15:55930835-55930836	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs375251863	chr15:55930884-55930885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368112528	chr15:55930897-55930898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371116403	chr15:55930911-55930912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185074341	chr15:55930926-55930927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188559138	chr15:55930984-55930985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532242403	chr15:55931024-55931025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540482161	chr15:55931042-55931043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552207252	chr15:55931078-55931079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142368109	chr15:55931106-55931107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377456966	chr15:55931117-55931118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535023557	chr15:55931126-55931127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145949885	chr15:55931128-55931129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74702941	chr15:55931153-55931154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561300520	chr15:55931154-55931155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568643869	chr15:55931157-55931158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571210627	chr15:55931161-55931162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539615327	chr15:55931179-55931180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs398027391	chr15:55931186-55931187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs398070667	chr15:55931189-55931190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74460741	chr15:55931205-55931206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557128126	chr15:55931243-55931244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79993336	chr15:55931268-55931269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546792671	chr15:55931274-55931275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116689371	chr15:55931283-55931284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74462286	chr15:55931340-55931341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78636167	chr15:55931347-55931348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573521696	chr15:55931373-55931374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541838485	chr15:55931375-55931376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561274003	chr15:55931387-55931388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531611961	chr15:55931400-55931401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs180711393	chr15:55931431-55931432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374717748	chr15:55931432-55931433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566782655	chr15:55931461-55931462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139502680	chr15:55931470-55931471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55902200-55942200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr15:55908600-55945000	Weak transcription	Left Ventricle	heart
3	chr15:55908800-55938800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr15:55910400-55930800	Weak transcription	Fetal Lung	lung
5	chr15:55911000-55931000	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr15:55911800-55977000	Weak transcription	Fetal Intestine Small	intestine
7	chr15:55912400-55944000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr15:55916000-55938200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr15:55918600-55931200	Weak transcription	Ovary	ovary
10	chr15:55920600-55931600	Weak transcription	Lung	lung
11	chr15:55920600-55933600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr15:55920600-55940000	Weak transcription	Psoas Muscle	Psoas
13	chr15:55920600-55953400	Weak transcription	HUVEC	blood vessel
14	chr15:55920800-55935200	Weak transcription	HSMMtube	muscle
15	chr15:55920800-55944600	Weak transcription	Primary hematopoietic stem cells	blood
16	chr15:55920800-55987600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr15:55921000-55936200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr15:55921200-55941400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr15:55923400-55930800	Weak transcription	A549	lung
20	chr15:55924000-55931800	Weak transcription	Brain Substantia Nigra	brain
21	chr15:55924200-55930600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr15:55924400-55944800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr15:55924600-55934600	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr15:55924800-55934600	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr15:55927600-55931800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr15:55927600-55932800	Strong transcription	Hela-S3	cervix
27	chr15:55928600-55932800	Strong transcription	Stomach Smooth Muscle	stomach
28	chr15:55928600-55933400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr15:55928800-55931000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr15:55928800-55931000	Weak transcription	Fetal Kidney	kidney
31	chr15:55928800-55932800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr15:55929000-55931200	Weak transcription	Fetal Muscle Leg	muscle
33	chr15:55929200-55932000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr15:55929400-55932800	Strong transcription	Placenta Amnion	Placenta Amnion
35	chr15:55929600-55931200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr15:55929600-55931200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr15:55929600-55931200	Weak transcription	Fetal Muscle Trunk	muscle
38	chr15:55929600-55931200	Weak transcription	Fetal Stomach	stomach
39	chr15:55929600-55933800	Strong transcription	HUES64 Cell Line	embryonic stem cell
40	chr15:55929800-55931800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr15:55929800-55932800	Strong transcription	HUES6 Cell Line	embryonic stem cell
42	chr15:55930200-55932400	Strong transcription	Placenta	Placenta
43	chr15:55930200-55933400	Strong transcription	Fetal Intestine Large	intestine
44	chr15:55930200-55933400	Strong transcription	HepG2	liver
45	chr15:55930400-55932000	Strong transcription	Cortex derived primary cultured neurospheres	brain
46	chr15:55930400-55933000	Weak transcription	Right Ventricle	heart
47	chr15:55930600-55932800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr15:55930800-55932600	Strong transcription	Fetal Lung	lung
49	chr15:55930800-55932800	Strong transcription	A549	lung
50	chr15:55931000-55932600	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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