Variant report

Variant	nsv569343
Chromosome Location	chr15:49531192-49547790
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	ATF1	chr15:49535098-49535236	K562	blood:	n/a	n/a
2	ATF3	chr15:49535104-49535341	K562	blood:	n/a	n/a
3	BACH1	chr15:49535125-49535374	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr15:49535202-49535371	K562	blood:	n/a	n/a
5	CEBPB	chr15:49535064-49535390	IMR90	lung:	n/a	n/a
6	CEBPB	chr15:49547716-49548421	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr15:49535180-49535330	HPF	lung:	n/a	n/a
8	CTCF	chr15:49535060-49535210	AG09319	gingival:	n/a	n/a
9	CTCF	chr15:49531440-49531590	SAEC	small airway:	n/a	n/a
10	CTCF	chr15:49533554-49533622	LNCaP	prostate:	n/a	n/a
11	CTCF	chr15:49535160-49535310	HPF	lung:	n/a	n/a
12	CTCF	chr15:49542318-49542350	Lung_OC	lung:	n/a	n/a
13	CTCF	chr15:49535140-49535290	HPAF	blood vessel:	n/a	n/a
14	CTCF	chr15:49535180-49535330	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr15:49535220-49535370	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr15:49535160-49535310	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr15:49535200-49535350	AG04450	lung:	n/a	n/a
18	CTCF	chr15:49535220-49535370	HBMEC	blood vessel:	n/a	n/a
19	CUX1	chr15:49537013-49537019	GM12878	blood:	n/a	n/a
20	EBF1	chr15:49536936-49536954	GM12878	blood:	n/a	n/a
21	EBF1	chr15:49541484-49541496	GM12878	blood:	n/a	n/a
22	EP300	chr15:49534748-49535905	SK-N-SH	brain:	n/a	n/a
23	EP300	chr15:49535000-49535356	K562	blood:	n/a	n/a
24	EP300	chr15:49534945-49535446	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr15:49529875-49532539	SK-N-SH	brain:	n/a	chr15:49531958-49531972 chr15:49530330-49530344
26	EP300	chr15:49535143-49535405	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr15:49534747-49535605	SK-N-SH	brain:	n/a	n/a
28	EP300	chr15:49534225-49534386	K562	blood:	n/a	n/a
29	FOS	chr15:49535152-49535398	MCF10A-Er-Src	breast:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
30	FOS	chr15:49535101-49535407	MCF10A-Er-Src	breast:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
31	FOS	chr15:49535137-49535318	MCF10A-Er-Src	breast:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
32	FOS	chr15:49535118-49535318	MCF10A-Er-Src	breast:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
33	FOSL1	chr15:49535051-49535486	K562	blood:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
34	FOSL2	chr15:49534870-49535797	SK-N-SH	brain:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
35	GATA3	chr15:49534535-49536032	SK-N-SH	brain:	n/a	chr15:49534711-49534721 chr15:49535268-49535275
36	GATA3	chr15:49546419-49546840	SK-N-SH	brain:	n/a	n/a
37	GATA3	chr15:49533679-49533850	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr15:49546155-49546232	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr15:49546222-49546752	SK-N-SH	brain:	n/a	n/a
40	GATA3	chr15:49534566-49535942	SK-N-SH	brain:	n/a	chr15:49534711-49534721 chr15:49535268-49535275
41	IRF1	chr15:49536988-49536993	K562	blood:	n/a	n/a
42	JUN	chr15:49534921-49535445	K562	blood:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
43	JUND	chr15:49535125-49535325	H1-hESC	embryonic stem cell:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
44	JUND	chr15:49534727-49536045	SK-N-SH	brain:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
45	JUND	chr15:49534817-49535607	SK-N-SH	brain:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
46	JUND	chr15:49534751-49536058	SK-N-SH	brain:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
47	JUND	chr15:49535069-49535443	K562	blood:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
48	MAFF	chr15:49534953-49535431	K562	blood:	n/a	n/a
49	MAFK	chr15:49534918-49535361	IMR90	lung:	n/a	n/a
50	MAFK	chr15:49535192-49535383	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:49534692-49534742	HCT-116	colon:	n/a
2	chr15:49535972-49536022	Hepatocyte	liver:	n/a
3	chr15:49534692-49534742	GM12878	blood:	n/a
4	chr15:49534692-49534742	BJ	skin:	n/a
5	chr15:49535972-49536022	AG09319	gingival:	n/a
6	chr15:49534692-49534742	T-47D	breast:	n/a
7	chr15:49535972-49536022	ovcar-3	ovarian:	n/a
8	chr15:49534692-49534742	H1-hESC	embryonic stem cell:	embryo
9	chr15:49534692-49534742	AG09319	gingival:	n/a
10	chr15:49534692-49534742	HRCEpiC	kidney:	n/a
11	chr15:49535972-49536022	BE2_C	brain:	n/a
12	chr15:49535972-49536022	LNCaP	prostate:	n/a
13	chr15:49535972-49536022	SAEC	small airway:	n/a
14	chr15:49535972-49536022	Jurkat	blood:	n/a
15	chr15:49535972-49536022	CMK	blood:	n/a
16	chr15:49534692-49534742	Hela-S3	cervix:	n/a
17	chr15:49535972-49536022	Caco-2	colon:	n/a
18	chr15:49535972-49536022	Hela-S3	cervix:	n/a
19	chr15:49534692-49534742	HL-60	blood:	n/a
20	chr15:49535972-49536022	HepG2	liver:	n/a
21	chr15:49534692-49534742	HUVEC	blood vessel:	n/a
22	chr15:49534692-49534742	SAEC	small airway:	n/a
23	chr15:49534692-49534742	NH-A	brain:	n/a
24	chr15:49535972-49536022	PANC-1	pancreas:	n/a
25	chr15:49534692-49534742	GM12892	blood:	n/a
26	chr15:49534692-49534742	HRE	kidney:	n/a
27	chr15:49535972-49536022	PrEC	prostate:	n/a
28	chr15:49534692-49534742	HCPEpiC	choroid plexus:	n/a
29	chr15:49534692-49534742	AG09309	skin:	n/a
30	chr15:49534692-49534742	HCF	heart:	n/a
31	chr15:49534692-49534742	HCM	heart:	n/a
32	chr15:49534692-49534742	HEK293	kidney:	embryo
33	chr15:49535972-49536022	T-47D	breast:	n/a
34	chr15:49534692-49534742	HepG2	liver:	n/a
35	chr15:49535972-49536022	HCPEpiC	choroid plexus:	n/a
36	chr15:49535972-49536022	HRE	kidney:	n/a
37	chr15:49534692-49534742	HPAEpiC	pulmonary alveolar:	n/a
38	chr15:49534692-49534742	GM06990	blood:	n/a
39	chr15:49534692-49534742	SK-N-SH_RA	brain:	n/a
40	chr15:49534692-49534742	GM19239	blood:	n/a
41	chr15:49535972-49536022	GM19239	blood:	n/a
42	chr15:49534692-49534742	IMR90	lung:	fetal
43	chr15:49535972-49536022	HL-60	blood:	n/a
44	chr15:49535972-49536022	HEEpiC	esophagus:	n/a
45	chr15:49535972-49536022	NHDF-neo	bronchial:	n/a
46	chr15:49535972-49536022	NH-A	brain:	n/a
47	chr15:49534692-49534742	NHDF-neo	bronchial:	n/a
48	chr15:49534692-49534742	LNCaP	prostate:	n/a
49	chr15:49535972-49536022	HMEC	breast:	n/a
50	chr15:49535972-49536022	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:49470915..49472999-chr15:49535845..49537993,2	K562	blood:
2	chr15:49461247..49464422-chr15:49530030..49534036,3	K562	blood:
3	chr15:49535482..49538280-chr15:49538929..49540490,2	K562	blood:
4	chr15:49541585..49543251-chr15:49545018..49547358,2	K562	blood:
5	chr15:49470039..49472415-chr15:49535845..49538837,2	K562	blood:
6	chr15:49533559..49535647-chr15:49536094..49538086,2	K562	blood:
7	chr15:49527986..49530632-chr15:49532231..49535128,2	K562	blood:
8	chr15:49535482..49538280-chr15:49538929..49540490,2	K562	blood:
9	chr15:49538461..49540714-chr15:49541925..49544059,3	K562	blood:
10	chr15:49541585..49543251-chr15:49545018..49547358,2	K562	blood:
11	chr15:49533559..49535647-chr15:49536094..49538086,2	K562	blood:
12	chr15:49538461..49540714-chr15:49541925..49544059,3	K562	blood:
13	chr15:49527930..49530105-chr15:49533812..49536591,2	MCF-7	breast:

Variant related genes	Relation type
GALK2	TF binding region
GALK2	CpG island
ENSG00000264210	chromatin interactions
ENSG00000259545	chromatin interactions
ENSG00000156958	chromatin interactions

Extended variants
information (count: 546 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:546 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs520949	chr15:49531192-49531193	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569080171	chr15:49531200-49531201	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs115965825	chr15:49531201-49531202	Weak transcription Flanking Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs550942328	chr15:49531202-49531203	Weak transcription Flanking Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs138635831	chr15:49531265-49531266	Weak transcription Flanking Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs557906413	chr15:49531333-49531334	Weak transcription Flanking Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs374091264	chr15:49531365-49531366	Weak transcription Flanking Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs199837168	chr15:49531406-49531407	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs148234101	chr15:49531427-49531428	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs372905837	chr15:49531438-49531439	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs201904223	chr15:49531485-49531486	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs531037984	chr15:49531492-49531493	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs573578687	chr15:49531510-49531511	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs374871677	chr15:49531526-49531527	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs544545223	chr15:49531534-49531535	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs141479055	chr15:49531537-49531538	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs201859172	chr15:49531571-49531572	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs200250817	chr15:49531603-49531604	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs201028160	chr15:49531605-49531606	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs376131074	chr15:49531643-49531644	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs533353269	chr15:49531671-49531672	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs111742323	chr15:49531705-49531706	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs76790767	chr15:49531713-49531714	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs74403369	chr15:49531714-49531715	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs552351082	chr15:49531731-49531732	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs543917303	chr15:49531733-49531734	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs181565072	chr15:49531738-49531739	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs185185062	chr15:49531755-49531756	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs561163340	chr15:49531774-49531775	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs531694969	chr15:49531779-49531780	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs190114826	chr15:49531816-49531817	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs569143603	chr15:49531934-49531935	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs539661959	chr15:49532024-49532025	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs551323121	chr15:49532025-49532026	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs566639740	chr15:49532060-49532061	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs533699542	chr15:49532065-49532066	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs555430637	chr15:49532082-49532083	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs573311393	chr15:49532157-49532158	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs537403635	chr15:49532162-49532163	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs376861157	chr15:49532176-49532177	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs548751224	chr15:49532179-49532180	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs112552812	chr15:49532195-49532196	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs181892200	chr15:49532274-49532275	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs545273345	chr15:49532350-49532351	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs560568903	chr15:49532411-49532412	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs572589943	chr15:49532430-49532431	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs571074402	chr15:49532441-49532442	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs186583908	chr15:49532481-49532482	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs529731073	chr15:49532488-49532489	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs540268998	chr15:49532513-49532514	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	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
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Aromatase excess syndrome	21470988	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:49463600-49540200	Weak transcription	Colonic Mucosa	Colon
2	chr15:49487200-49531200	Weak transcription	HMEC	breast
3	chr15:49492000-49539400	Weak transcription	Small Intestine	intestine
4	chr15:49508800-49535800	Weak transcription	A549	lung
5	chr15:49510000-49541800	Weak transcription	NHEK	skin
6	chr15:49510200-49537000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr15:49510800-49534400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr15:49511800-49531400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr15:49511800-49532200	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr15:49516000-49531400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr15:49518000-49535400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr15:49518000-49541000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr15:49518200-49548600	Weak transcription	Aorta	Aorta
14	chr15:49518600-49532000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr15:49518600-49557600	Weak transcription	Esophagus	oesophagus
16	chr15:49518800-49539200	Weak transcription	Ovary	ovary
17	chr15:49520400-49595600	Weak transcription	Right Ventricle	heart
18	chr15:49520600-49531200	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr15:49520800-49531400	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr15:49522000-49534600	Weak transcription	Fetal Muscle Trunk	muscle
21	chr15:49522000-49537800	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr15:49522000-49538200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr15:49522000-49540400	Weak transcription	Stomach Mucosa	stomach
24	chr15:49522200-49531400	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr15:49522200-49535000	Weak transcription	Left Ventricle	heart
26	chr15:49522400-49559400	Weak transcription	Pancreas	Pancrea
27	chr15:49522600-49534400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr15:49522600-49535200	Weak transcription	Gastric	stomach
29	chr15:49522800-49531400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:49523800-49534800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr15:49523800-49540200	Weak transcription	Spleen	Spleen
32	chr15:49524600-49531400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr15:49524600-49531400	Weak transcription	Duodenum Mucosa	Duodenum
34	chr15:49524600-49531400	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr15:49524600-49535200	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr15:49524600-49535200	Weak transcription	Placenta	Placenta
37	chr15:49524600-49535200	Weak transcription	Thymus	Thymus
38	chr15:49524600-49539200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr15:49524600-49544800	Weak transcription	Lung	lung
40	chr15:49524800-49531400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr15:49525000-49531400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr15:49525000-49534600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr15:49525200-49531400	Weak transcription	Primary B cells from peripheral blood	blood
44	chr15:49525200-49531400	Weak transcription	HepG2	liver
45	chr15:49525200-49535000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr15:49525200-49535000	Weak transcription	Fetal Intestine Large	intestine
47	chr15:49525400-49535200	Weak transcription	Fetal Intestine Small	intestine
48	chr15:49526200-49531200	Weak transcription	Primary B cells from cord blood	blood
49	chr15:49526200-49531200	Weak transcription	Primary T cells from cord blood	blood
50	chr15:49526200-49534600	Weak transcription	K562	blood

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