Variant report

Variant	nsv569578
Chromosome Location	chr15:57495060-57559387
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:620)
CpG islands
(count:550)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:57505978-57506359	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:57513442-57513550	K562	blood:	n/a	n/a
3	ARID3A	chr15:57508438-57509141	K562	blood:	n/a	n/a
4	ATF1	chr15:57506050-57506415	K562	blood:	n/a	n/a
5	ATF1	chr15:57545357-57545655	K562	blood:	n/a	n/a
6	ATF1	chr15:57537532-57537731	K562	blood:	n/a	n/a
7	ATF2	chr15:57551562-57552061	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr15:57551652-57551978	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr15:57545350-57545682	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:57515774-57515890	K562	blood:	n/a	n/a
11	BCL11A	chr15:57529462-57529717	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr15:57506145-57506339	GM12878	blood:	n/a	n/a
13	BHLHE40	chr15:57520812-57520828	K562	blood:	n/a	n/a
14	BHLHE40	chr15:57515634-57515995	GM12878	blood:	n/a	n/a
15	CCNT2	chr15:57538181-57538342	K562	blood:	n/a	n/a
16	CCNT2	chr15:57508308-57508690	K562	blood:	n/a	n/a
17	CEBPB	chr15:57545311-57545691	K562	blood:	n/a	chr15:57545493-57545504
18	CEBPB	chr15:57505913-57506466	A549	lung:	n/a	n/a
19	CEBPB	chr15:57532992-57533138	IMR90	lung:	n/a	n/a
20	CEBPB	chr15:57555890-57555949	K562	blood:	n/a	n/a
21	CEBPB	chr15:57545329-57545629	ECC-1	luminal epithelium:	n/a	chr15:57545493-57545504
22	CEBPB	chr15:57542114-57542144	K562	blood:	n/a	n/a
23	CEBPB	chr15:57545228-57545678	H1-hESC	embryonic stem cell:	n/a	chr15:57545493-57545504
24	CEBPB	chr15:57545326-57545678	IMR90	lung:	n/a	chr15:57545493-57545504
25	CEBPB	chr15:57519752-57519771	K562	blood:	n/a	n/a
26	CEBPB	chr15:57506095-57506290	K562	blood:	n/a	n/a
27	CEBPB	chr15:57506025-57506388	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr15:57545376-57545586	K562	blood:	n/a	chr15:57545493-57545504
29	CEBPB	chr15:57528122-57528384	IMR90	lung:	n/a	n/a
30	CEBPB	chr15:57506039-57506402	HepG2	liver:	n/a	n/a
31	CEBPB	chr15:57506004-57506380	K562	blood:	n/a	n/a
32	CEBPB	chr15:57544222-57544607	IMR90	lung:	n/a	n/a
33	CEBPB	chr15:57506027-57506379	A549	lung:	n/a	n/a
34	CEBPB	chr15:57531920-57531938	A549	lung:	n/a	n/a
35	CEBPB	chr15:57545329-57545657	A549	lung:	n/a	chr15:57545493-57545504
36	CEBPB	chr15:57545352-57545665	HepG2	liver:	n/a	chr15:57545493-57545504
37	CEBPB	chr15:57511080-57511632	IMR90	lung:	n/a	n/a
38	CEBPB	chr15:57505981-57506328	A549	lung:	n/a	n/a
39	CEBPB	chr15:57505926-57506405	K562	blood:	n/a	n/a
40	CEBPB	chr15:57505982-57506352	MCF-7	breast:	n/a	n/a
41	CEBPB	chr15:57505970-57506467	MCF-7	breast:	n/a	n/a
42	CEBPB	chr15:57505963-57506377	IMR90	lung:	n/a	n/a
43	CEBPB	chr15:57545398-57545669	MCF-7	breast:	n/a	chr15:57545493-57545504
44	CEBPB	chr15:57545298-57545686	K562	blood:	n/a	chr15:57545493-57545504
45	CEBPB	chr15:57506004-57506326	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr15:57520727-57520766	K562	blood:	n/a	n/a
47	CHD1	chr15:57511110-57511118	GM12878	blood:	n/a	n/a
48	CHD1	chr15:57511374-57511694	GM12878	blood:	n/a	n/a
49	CHD1	chr15:57511348-57511755	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr15:57551731-57552167	GM12878	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:57519802-57519852	A549	lung:	n/a
2	chr15:57519802-57519852	A549	lung:	n/a
3	chr15:57537929-57537979	NHBE	bronchial:	n/a
4	chr15:57537929-57537979	GM12878	blood:	n/a
5	chr15:57537929-57537979	GM12891	blood:	n/a
6	chr15:57528690-57528740	HCM	heart:	n/a
7	chr15:57537929-57537979	ovcar-3	ovarian:	n/a
8	chr15:57510460-57510510	HEEpiC	esophagus:	n/a
9	chr15:57519802-57519852	SAEC	small airway:	n/a
10	chr15:57510284-57510334	GM12891	blood:	n/a
11	chr15:57510460-57510510	MCF10A-Er-Src	breast:	n/a
12	chr15:57544645-57544695	SAEC	small airway:	n/a
13	chr15:57544645-57544695	U87	brain:	n/a
14	chr15:57508437-57508487	GM19239	blood:	n/a
15	chr15:57510460-57510510	SK-N-SH	brain:	n/a
16	chr15:57508437-57508487	HEEpiC	esophagus:	n/a
17	chr15:57510575-57510625	LNCaP	prostate:	n/a
18	chr15:57510284-57510334	MCF10A-Er-Src	breast:	n/a
19	chr15:57537929-57537979	HL-60	blood:	n/a
20	chr15:57510284-57510334	HEEpiC	esophagus:	n/a
21	chr15:57510575-57510625	Hela-S3	cervix:	n/a
22	chr15:57510575-57510625	AG10803	skin:	n/a
23	chr15:57544645-57544695	K562	blood:	n/a
24	chr15:57544645-57544695	HMEC	breast:	n/a
25	chr15:57510460-57510510	ProgFib	skin:	n/a
26	chr15:57551709-57551759	ovcar-3	ovarian:	n/a
27	chr15:57510284-57510334	PFSK-1	brain:	n/a
28	chr15:57528690-57528740	AG10803	skin:	n/a
29	chr15:57528690-57528740	NHBE	bronchial:	n/a
30	chr15:57508437-57508487	SAEC	small airway:	n/a
31	chr15:57544645-57544695	HUVEC	blood vessel:	n/a
32	chr15:57510460-57510510	HCT-116	colon:	n/a
33	chr15:57508437-57508487	HRPEpiC	eye:	n/a
34	chr15:57508437-57508487	IMR90	lung:	fetal
35	chr15:57510460-57510510	HRCEpiC	kidney:	n/a
36	chr15:57510460-57510510	NT2-D1	testis:	n/a
37	chr15:57537929-57537979	Hepatocyte	liver:	n/a
38	chr15:57519802-57519852	SKMC	muscle:	n/a
39	chr15:57528690-57528740	SK-N-SH_RA	brain:	n/a
40	chr15:57544645-57544695	HepG2	liver:	n/a
41	chr15:57544645-57544695	HEEpiC	esophagus:	n/a
42	chr15:57508437-57508487	HL-60	blood:	n/a
43	chr15:57510284-57510334	NHBE	bronchial:	n/a
44	chr15:57510284-57510334	AG04449	skin:	fetal
45	chr15:57537929-57537979	AoSMC	blood vessel:	n/a
46	chr15:57510284-57510334	NHDF-neo	bronchial:	n/a
47	chr15:57537929-57537979	HepG2	liver:	n/a
48	chr15:57508437-57508487	HIPEpiC	eye:	n/a
49	chr15:57528690-57528740	T-47D	breast:	n/a
50	chr15:57528690-57528740	ECC-1	luminal epithelium:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:57499998..57502401-chr15:57504758..57507480,2	K562	blood:
2	chr15:57489296..57493196-chr15:57493593..57496438,4	K562	blood:
3	chr15:57514341..57517314-chr15:57518774..57520989,2	MCF-7	breast:
4	chr15:57514341..57517314-chr15:57518774..57520989,2	MCF-7	breast:
5	chr15:57510591..57512742-chr15:57523126..57525125,2	K562	blood:
6	chr15:57506333..57510182-chr15:57512015..57516171,5	K562	blood:
7	chr15:57501824..57503369-chr15:57505657..57507843,2	K562	blood:
8	chr15:57518271..57520593-chr15:57524473..57526151,2	K562	blood:
9	chr15:57548444..57552670-chr15:57553195..57556981,4	K562	blood:
10	chr15:57539799..57542087-chr15:57542689..57545478,3	K562	blood:
11	chr15:57516204..57519771-chr15:57520107..57524216,4	K562	blood:
12	chr15:57508073..57512585-chr15:57540435..57543693,4	K562	blood:
13	chr15:57485138..57486752-chr15:57494991..57496956,2	K562	blood:
14	chr15:57519601..57521233-chr15:57537567..57539134,2	K562	blood:
15	chr15:57507579..57509152-chr15:57511369..57513515,2	K562	blood:
16	chr15:57548795..57550797-chr15:57550821..57552901,2	K562	blood:
17	chr15:57501438..57503633-chr15:57503718..57505515,2	MCF-7	breast:
18	chr15:57549403..57551171-chr15:57553195..57555011,2	K562	blood:
19	chr15:57543333..57548085-chr15:57548138..57552930,5	K562	blood:
20	chr15:57523231..57525138-chr15:57581607..57583669,2	K562	blood:
21	chr15:57511815..57513845-chr15:57528916..57531041,2	K562	blood:
22	chr15:57543547..57545308-chr15:57547959..57549638,2	K562	blood:
23	chr15:57491334..57495003-chr15:57497716..57500211,4	K562	blood:
24	chr15:57516204..57519771-chr15:57520107..57524216,4	K562	blood:
25	chr15:57508073..57512585-chr15:57540435..57543693,4	K562	blood:
26	chr15:57511242..57514182-chr15:57522770..57524626,2	K562	blood:
27	chr15:57539046..57541393-chr15:57548730..57551429,2	MCF-7	breast:
28	chr15:57511490..57513273-chr15:57516497..57519012,2	K562	blood:
29	chr15:57546353..57548188-chr15:57549321..57552390,3	K562	blood:
30	chr15:57539799..57542087-chr15:57542689..57545478,3	K562	blood:
31	chr15:57546353..57548188-chr15:57549321..57552390,3	K562	blood:
32	chr15:57548795..57550797-chr15:57550821..57552901,2	K562	blood:
33	chr15:57549292..57551401-chr15:57555481..57557548,2	K562	blood:
34	chr15:57532165..57533067-chr3:23958389..23959122,2	NB4	blood:
35	chr15:57511815..57513845-chr15:57528916..57531041,2	K562	blood:
36	chr15:57524385..57526174-chr15:57527387..57529513,2	K562	blood:
37	chr15:57505273..57507869-chr15:57520265..57523117,2	K562	blood:
38	chr15:57548444..57552670-chr15:57553195..57556981,4	K562	blood:
39	chr15:57519601..57521233-chr15:57537567..57539134,2	K562	blood:
40	chr15:57210007..57212139-chr15:57506855..57509389,2	K562	blood:
41	chr15:57524385..57526174-chr15:57527387..57529513,2	K562	blood:
42	chr15:57506333..57510182-chr15:57512015..57516171,5	K562	blood:
43	chr15:57518271..57520593-chr15:57524473..57526151,2	K562	blood:
44	chr15:57549292..57551401-chr15:57555481..57557548,2	K562	blood:
45	chr15:57463088..57465756-chr15:57508585..57510347,2	K562	blood:
46	chr15:57501438..57503633-chr15:57503718..57505515,2	MCF-7	breast:
47	chr15:57549403..57551171-chr15:57553195..57555011,2	K562	blood:

No data

Variant related genes	Relation type
HNRNPA3P11	TF binding region
TCF12	TF binding region
HNRNPA3P11	CpG island
TCF12	CpG island
ENSG00000174748	chromatin interactions
ENSG00000197885	chromatin interactions
ENSG00000260689	chromatin interactions
ENSG00000140262	chromatin interactions
ENSG00000137871	chromatin interactions

Extended variants
information (count: 2636 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2636 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12050751	chr15:57495060-57495061	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190855680	chr15:57495080-57495081	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539824086	chr15:57495081-57495082	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs71478618	chr15:57495082-57495083	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560442843	chr15:57495090-57495091	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543614313	chr15:57495114-57495115	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148651752	chr15:57495130-57495131	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs12903115	chr15:57495151-57495152	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs2593223	chr15:57495154-57495155	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs112771389	chr15:57495190-57495191	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370730804	chr15:57495198-57495199	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530931396	chr15:57495248-57495249	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs16977306	chr15:57495252-57495253	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs570843837	chr15:57495253-57495254	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112321866	chr15:57495257-57495258	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111966310	chr15:57495266-57495267	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546677224	chr15:57495285-57495286	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115530068	chr15:57495291-57495292	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs114502507	chr15:57495292-57495293	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12050758	chr15:57495303-57495304	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs575878791	chr15:57495342-57495343	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538426207	chr15:57495398-57495399	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs557862107	chr15:57495419-57495420	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577660828	chr15:57495442-57495443	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79065819	chr15:57495465-57495466	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2703598	chr15:57495472-57495473	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559852431	chr15:57495482-57495483	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573599370	chr15:57495505-57495506	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116121593	chr15:57495511-57495512	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181912351	chr15:57495568-57495569	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531438672	chr15:57495586-57495587	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs9672565	chr15:57495595-57495596	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551267786	chr15:57495623-57495624	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2591068	chr15:57495687-57495688	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs150788826	chr15:57495703-57495704	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139211633	chr15:57495714-57495715	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372827876	chr15:57495725-57495726	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552792911	chr15:57495741-57495742	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566826289	chr15:57495783-57495784	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186940989	chr15:57495790-57495791	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2733309	chr15:57495813-57495814	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs35675279	chr15:57495818-57495819	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569549012	chr15:57495864-57495865	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191331898	chr15:57495885-57495886	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35954723	chr15:57495901-57495902	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558058752	chr15:57495939-57495940	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577676038	chr15:57495971-57495972	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183186144	chr15:57495972-57495973	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144191072	chr15:57495990-57495991	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375530464	chr15:57496065-57496066	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Gastrointestinal stromal cancer	16982739	CNVD
Chronic lymphocytic leukemia	21546498	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
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2413 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57444400-57507400	Weak transcription	K562	blood
2	chr15:57453800-57524600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr15:57457200-57499400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr15:57458200-57505200	Strong transcription	Fetal Thymus	thymus
5	chr15:57478800-57526200	Weak transcription	Hela-S3	cervix
6	chr15:57479400-57524800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr15:57481800-57524600	Weak transcription	Right Ventricle	heart
8	chr15:57484800-57496200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr15:57484800-57502000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr15:57485000-57501000	Weak transcription	Spleen	Spleen
11	chr15:57485000-57501800	Weak transcription	Lung	lung
12	chr15:57485000-57506200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr15:57485600-57505000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr15:57486600-57496000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr15:57486800-57505800	Weak transcription	NHDF-Ad	bronchial
16	chr15:57487000-57496600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr15:57487000-57524400	Weak transcription	Placenta	Placenta
18	chr15:57487200-57503000	Weak transcription	Liver	Liver
19	chr15:57487200-57511200	Weak transcription	Fetal Muscle Trunk	muscle
20	chr15:57488200-57511600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr15:57488400-57496000	Weak transcription	Primary hematopoietic stem cells	blood
22	chr15:57488400-57496000	Weak transcription	Fetal Intestine Small	intestine
23	chr15:57489200-57496000	Weak transcription	Osteobl	bone
24	chr15:57489200-57506000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr15:57489400-57506200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr15:57490600-57505800	Weak transcription	NH-A	brain
27	chr15:57490800-57496400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr15:57491000-57501400	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr15:57491000-57505600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr15:57491000-57506000	Weak transcription	HMEC	breast
31	chr15:57491200-57508000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr15:57491400-57496000	Weak transcription	Ovary	ovary
33	chr15:57491400-57497200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr15:57491400-57497200	Weak transcription	Right Atrium	heart
35	chr15:57491400-57497800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr15:57491400-57500800	Weak transcription	Thymus	Thymus
37	chr15:57491400-57501200	Weak transcription	Primary B cells from cord blood	blood
38	chr15:57491400-57503000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr15:57491400-57503000	Weak transcription	Primary T cells from cord blood	blood
40	chr15:57491400-57503200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr15:57491400-57505800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr15:57491400-57505800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr15:57491400-57506000	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr15:57491400-57506200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr15:57491400-57510000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr15:57491400-57510000	Weak transcription	Psoas Muscle	Psoas
47	chr15:57491400-57510200	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr15:57491400-57511200	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr15:57491600-57496000	Weak transcription	Brain Cingulate Gyrus	brain
50	chr15:57491600-57498400	Weak transcription	Rectal Mucosa Donor 29	rectum

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