Variant report

Variant	nsv976926
Chromosome Location	chr15:42202094-42217599
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:287)
CpG islands
(count:671)
Chromatin interactive
region (count:24)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:42209865-42210212	K562	blood:	n/a	n/a
2	ATF3	chr15:42209948-42210244	K562	blood:	n/a	n/a
3	ATF3	chr15:42209926-42210199	K562	blood:	n/a	n/a
4	BCL3	chr15:42211264-42211459	GM12878	blood:	n/a	n/a
5	BCL3	chr15:42210242-42210587	GM12878	blood:	n/a	n/a
6	BCL3	chr15:42210289-42210635	GM12878	blood:	n/a	n/a
7	BHLHE40	chr15:42209895-42210418	K562	blood:	n/a	chr15:42210169-42210185
8	CBX3	chr15:42209863-42210275	K562	blood:	n/a	n/a
9	CCNT2	chr15:42210018-42210207	K562	blood:	n/a	n/a
10	CEBPB	chr15:42202122-42202135	HepG2	liver:	n/a	n/a
11	CEBPB	chr15:42215724-42215988	IMR90	lung:	n/a	n/a
12	CEBPB	chr15:42214641-42214975	HepG2	liver:	n/a	chr15:42214823-42214834
13	CEBPB	chr15:42214696-42214903	HepG2	liver:	n/a	chr15:42214823-42214834
14	CEBPB	chr15:42207626-42207912	HepG2	liver:	n/a	n/a
15	CTCF	chr15:42208760-42208910	GM12864	blood:	n/a	chr15:42208852-42208860
16	CTCF	chr15:42208660-42208810	RPTEC	kidney:	n/a	n/a
17	CTCF	chr15:42208883-42208902	MCF-7	breast:	n/a	n/a
18	CTCF	chr15:42208840-42208990	GM12867	blood:	n/a	chr15:42208852-42208860
19	CTCF	chr15:42208811-42208919	GM10266	blood:	n/a	chr15:42208852-42208860
20	CTCF	chr15:42208844-42208903	GM19240	blood:	n/a	chr15:42208852-42208860
21	CTCF	chr15:42208725-42208984	GM12878	blood:	n/a	chr15:42208852-42208860
22	CTCF	chr15:42208700-42208850	K562	blood:	n/a	n/a
23	CTCF	chr15:42208760-42208910	GM12871	blood:	n/a	chr15:42208852-42208860
24	CTCF	chr15:42208780-42208930	HBMEC	blood vessel:	n/a	chr15:42208852-42208860
25	CTCF	chr15:42208340-42208490	HRE	kidney:	n/a	n/a
26	CTCF	chr15:42213220-42213370	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr15:42208740-42208890	HBMEC	blood vessel:	n/a	chr15:42208852-42208860
28	CTCF	chr15:42208815-42208874	GM12878	blood:	n/a	chr15:42208852-42208860
29	CTCF	chr15:42208800-42208950	GM12873	blood:	n/a	chr15:42208852-42208860
30	CTCF	chr15:42208760-42208910	GM12868	blood:	n/a	chr15:42208852-42208860
31	CTCF	chr15:42208860-42209010	HMEC	breast:	n/a	n/a
32	CTCF	chr15:42208814-42208951	GM12891	blood:	n/a	chr15:42208852-42208860
33	CTCF	chr15:42208440-42208590	HMEC	breast:	n/a	n/a
34	CTCF	chr15:42208740-42208890	GM12868	blood:	n/a	chr15:42208852-42208860
35	CTCF	chr15:42208780-42208930	GM12873	blood:	n/a	chr15:42208852-42208860
36	CTCF	chr15:42208800-42208950	GM12870	blood:	n/a	chr15:42208852-42208860
37	CTCF	chr15:42208760-42208910	HL-60	blood:	n/a	chr15:42208852-42208860
38	CTCF	chr15:42208740-42208890	GM12872	blood:	n/a	chr15:42208852-42208860
39	CTCF	chr15:42208780-42208930	HMEC	breast:	n/a	chr15:42208852-42208860
40	CTCF	chr15:42208777-42208895	Lung_OC	lung:	n/a	chr15:42208852-42208860
41	CTCF	chr15:42208783-42208980	GM19239	blood:	n/a	chr15:42208852-42208860
42	CTCF	chr15:42208760-42208910	GM12874	blood:	n/a	chr15:42208852-42208860
43	CTCF	chr15:42208783-42208950	Kidney_OC	kidney:	n/a	chr15:42208852-42208860
44	CTCF	chr15:42208780-42208930	HRE	kidney:	n/a	chr15:42208852-42208860
45	CTCF	chr15:42208760-42208910	GM12866	blood:	n/a	chr15:42208852-42208860
46	CTCF	chr15:42205399-42205489	GM12892	blood:	n/a	n/a
47	CTCF	chr15:42208800-42208950	GM12874	blood:	n/a	chr15:42208852-42208860
48	CTCF	chr15:42208720-42208870	GM12871	blood:	n/a	chr15:42208852-42208860
49	CTCF	chr15:42208769-42208930	GM10248	blood:	n/a	chr15:42208852-42208860
50	CTCF	chr15:42208820-42208970	GM12869	blood:	n/a	chr15:42208852-42208860

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42213760-42213810	LNCaP	prostate:	n/a
2	chr15:42209202-42209252	SK-N-SH_RA	brain:	n/a
3	chr15:42213760-42213810	NT2-D1	testis:	n/a
4	chr15:42209202-42209252	MCF10A-Er-Src	breast:	n/a
5	chr15:42211437-42211487	K562	blood:	n/a
6	chr15:42211581-42211631	PFSK-1	brain:	n/a
7	chr15:42211679-42211729	BJ	skin:	n/a
8	chr15:42211679-42211729	HAEpiC	amniotic membrane:	n/a
9	chr15:42211840-42211890	IMR90	lung:	fetal
10	chr15:42211581-42211631	U87	brain:	n/a
11	chr15:42211581-42211631	BE2_C	brain:	n/a
12	chr15:42210119-42210169	Hela-S3	cervix:	n/a
13	chr15:42211437-42211487	T-47D	breast:	n/a
14	chr15:42213760-42213810	RPTEC	kidney:	n/a
15	chr15:42211689-42211739	HAEpiC	amniotic membrane:	n/a
16	chr15:42211520-42211570	HNPCEpiC	eye:	n/a
17	chr15:42209178-42209228	ovcar-3	ovarian:	n/a
18	chr15:42209178-42209228	HCT-116	colon:	n/a
19	chr15:42211509-42211559	AG10803	skin:	n/a
20	chr15:42211509-42211559	MCF-7	breast:	n/a
21	chr15:42211509-42211559	HCT-116	colon:	n/a
22	chr15:42209178-42209228	H1-hESC	embryonic stem cell:	embryo
23	chr15:42211520-42211570	AG10803	skin:	n/a
24	chr15:42210119-42210169	IMR90	lung:	fetal
25	chr15:42211679-42211729	HCF	heart:	n/a
26	chr15:42209178-42209228	HRCEpiC	kidney:	n/a
27	chr15:42209178-42209228	Hela-S3	cervix:	n/a
28	chr15:42211520-42211570	U87	brain:	n/a
29	chr15:42210119-42210169	HL-60	blood:	n/a
30	chr15:42211509-42211559	H1-hESC	embryonic stem cell:	embryo
31	chr15:42211679-42211729	AoSMC	blood vessel:	n/a
32	chr15:42211581-42211631	Caco-2	colon:	n/a
33	chr15:42211840-42211890	K562	blood:	n/a
34	chr15:42211689-42211739	NH-A	brain:	n/a
35	chr15:42211437-42211487	HEK293	kidney:	embryo
36	chr15:42210119-42210169	GM19239	blood:	n/a
37	chr15:42211679-42211729	AG10803	skin:	n/a
38	chr15:42210119-42210169	ECC-1	luminal epithelium:	n/a
39	chr15:42213760-42213810	HRE	kidney:	n/a
40	chr15:42209202-42209252	HNPCEpiC	eye:	n/a
41	chr15:42211689-42211739	GM12891	blood:	n/a
42	chr15:42211679-42211729	NH-A	brain:	n/a
43	chr15:42213760-42213810	AG04449	skin:	fetal
44	chr15:42213760-42213810	MCF-7	breast:	n/a
45	chr15:42211689-42211739	SK-N-SH_RA	brain:	n/a
46	chr15:42209202-42209252	NB4	blood:	n/a
47	chr15:42211509-42211559	Hepatocyte	liver:	n/a
48	chr15:42211840-42211890	HCM	heart:	n/a
49	chr15:42209178-42209228	NB4	blood:	n/a
50	chr15:42211509-42211559	Hela-S3	cervix:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:42203961..42205680-chr15:42206094..42208991,2	K562	blood:
2	chr15:42215883..42217701-chr15:42220776..42223208,2	K562	blood:
3	chr15:42212088..42214945-chr15:42215453..42219644,3	K562	blood:
4	chr15:42212123..42215123-chr15:42215453..42219644,4	K562	blood:
5	chr15:42200852..42203519-chr15:42209900..42211491,2	K562	blood:
6	chr15:42148784..42150939-chr15:42202289..42204151,2	MCF-7	breast:
7	chr15:42215835..42217701-chr15:42219642..42223208,3	K562	blood:
8	chr15:42202438..42205069-chr15:42210826..42212891,2	MCF-7	breast:
9	chr15:42200541..42203413-chr15:42204605..42206886,2	K562	blood:
10	chr15:42207550..42209850-chr15:42209914..42212582,2	MCF-7	breast:
11	chr15:42217107..42219437-chr15:42264184..42266098,2	MCF-7	breast:
12	chr15:42185754..42187828-chr15:42203844..42205813,2	K562	blood:
13	chr15:42208548..42210300-chr15:42220851..42222621,2	K562	blood:
14	chr15:42217369..42219216-chr15:42220643..42223205,3	MCF-7	breast:
15	chr15:42202438..42205069-chr15:42210826..42212891,2	MCF-7	breast:
16	chr15:42196907..42199684-chr15:42201909..42205293,3	K562	blood:
17	chr15:42207550..42209850-chr15:42209914..42212582,2	MCF-7	breast:
18	chr15:42209684..42211751-chr15:42216402..42218970,2	MCF-7	breast:
19	chr15:42186555..42188627-chr15:42217363..42219299,2	K562	blood:
20	chr15:42209684..42211751-chr15:42216402..42218970,2	MCF-7	breast:
21	chr15:42200852..42203519-chr15:42209900..42211491,2	K562	blood:
22	chr15:42182721..42185354-chr15:42206031..42208454,3	K562	blood:
23	chr15:42203961..42205680-chr15:42206094..42208991,2	K562	blood:
24	chr15:42200541..42203413-chr15:42204605..42206886,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-JMJD7-PLA2G4B-3	chr15:42213615-42213939	ENSG00000259883.1

No data

Variant related genes	Relation type
ENSG00000259883	TF binding region
ENSG00000259883	CpG island
ENSG00000259883	chromatin interactions
ENSG00000103966	chromatin interactions
ENSG00000174171	chromatin interactions
ENSG00000246740	chromatin interactions
ENSG00000137877	chromatin interactions

Extended variants
information (count: 669 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151087664	chr15:42202095-42202096	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs533151785	chr15:42202119-42202120	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs549569556	chr15:42202120-42202121	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs563435318	chr15:42202125-42202126	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs376214140	chr15:42202130-42202131	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs528856549	chr15:42202142-42202143	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs548598437	chr15:42202169-42202170	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs566020729	chr15:42202192-42202193	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs528727793	chr15:42202205-42202206	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552073668	chr15:42202211-42202212	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376355842	chr15:42202234-42202235	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571702712	chr15:42202264-42202265	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537663203	chr15:42202272-42202273	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557165989	chr15:42202316-42202317	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs73408598	chr15:42202347-42202348	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536631133	chr15:42202350-42202351	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532629060	chr15:42202470-42202471	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140267050	chr15:42202568-42202569	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553368981	chr15:42202569-42202570	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs142586066	chr15:42202588-42202589	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541278241	chr15:42202639-42202640	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs74619394	chr15:42202643-42202644	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs28547280	chr15:42202647-42202648	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs543646780	chr15:42202672-42202673	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144281731	chr15:42202737-42202738	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528990428	chr15:42202747-42202748	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201982603	chr15:42202770-42202771	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542332461	chr15:42202792-42202793	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147806703	chr15:42202794-42202795	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528079667	chr15:42202842-42202843	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551748493	chr15:42202869-42202870	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571949845	chr15:42202892-42202893	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186883284	chr15:42202902-42202903	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141245426	chr15:42202956-42202957	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113730807	chr15:42202981-42202982	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554277596	chr15:42202986-42202987	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs200571133	chr15:42203010-42203011	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs201297683	chr15:42203021-42203022	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs199784508	chr15:42203027-42203028	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200907044	chr15:42203028-42203029	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs137906044	chr15:42203089-42203090	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191850423	chr15:42203140-42203141	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149100523	chr15:42203144-42203145	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567039668	chr15:42203166-42203167	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs78448989	chr15:42203178-42203179	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143205785	chr15:42203182-42203183	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557762673	chr15:42203280-42203281	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138664512	chr15:42203303-42203304	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141785577	chr15:42203382-42203383	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557086685	chr15:42203391-42203392	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	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
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:936 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42187200-42211800	Weak transcription	Small Intestine	intestine
2	chr15:42187600-42209800	Weak transcription	Colon Smooth Muscle	Colon
3	chr15:42187800-42206800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr15:42188600-42209600	Strong transcription	NHEK	skin
5	chr15:42189800-42208400	Strong transcription	HUVEC	blood vessel
6	chr15:42190200-42209800	Weak transcription	Hela-S3	cervix
7	chr15:42190400-42218600	Weak transcription	Fetal Lung	lung
8	chr15:42192600-42204000	Strong transcription	Esophagus	oesophagus
9	chr15:42195800-42209000	Strong transcription	Sigmoid Colon	Sigmoid Colon
10	chr15:42197200-42202600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr15:42197200-42204800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr15:42197200-42209800	Weak transcription	A549	lung
13	chr15:42197200-42210400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr15:42197200-42210800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr15:42197200-42218600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr15:42197400-42205200	Weak transcription	Brain Angular Gyrus	brain
17	chr15:42197400-42206600	Strong transcription	NHLF	lung
18	chr15:42197400-42206800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr15:42197400-42208200	Strong transcription	HSMM	muscle
20	chr15:42197400-42209600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr15:42197400-42218600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr15:42197600-42202200	Strong transcription	Duodenum Smooth Muscle	Duodenum
23	chr15:42197600-42202800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr15:42197600-42202800	Strong transcription	HSMMtube	muscle
25	chr15:42197600-42204000	Weak transcription	Right Atrium	heart
26	chr15:42197600-42206400	Weak transcription	Psoas Muscle	Psoas
27	chr15:42197800-42202600	Strong transcription	Liver	Liver
28	chr15:42197800-42206800	Strong transcription	Primary T cells from cord blood	blood
29	chr15:42197800-42208200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr15:42198000-42202200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr15:42198200-42202200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr15:42198200-42202600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr15:42198200-42206600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr15:42198200-42207000	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr15:42198200-42212000	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr15:42198400-42203200	Strong transcription	Fetal Muscle Leg	muscle
37	chr15:42198600-42202200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
38	chr15:42198600-42202200	Strong transcription	H9 Cell Line	embryonic stem cell
39	chr15:42198600-42202200	Strong transcription	Colonic Mucosa	Colon
40	chr15:42198600-42202200	Strong transcription	Stomach Smooth Muscle	stomach
41	chr15:42198600-42202200	Strong transcription	Osteobl	bone
42	chr15:42198600-42202400	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr15:42198600-42202400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
44	chr15:42198600-42202600	Strong transcription	Primary T helper cells PMA-I stimulated	--
45	chr15:42198600-42204600	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr15:42198800-42202200	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr15:42198800-42202200	Strong transcription	Duodenum Mucosa	Duodenum
48	chr15:42198800-42202400	Strong transcription	HMEC	breast
49	chr15:42198800-42204000	Strong transcription	Primary B cells from cord blood	blood
50	chr15:42198800-42212000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood

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