Variant report

Variant	esv1008860
Chromosome Location	chr15:42113556-42117710
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	CEBPB	chr15:42117679-42117994	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr15:42115328-42115776	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
3	CTCF	chr15:42115440-42115590	HEK293	kidney:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
4	CTCF	chr15:42115460-42115610	HPAF	blood vessel:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
5	CTCF	chr15:42115487-42115562	GM12892	blood:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
6	CTCF	chr15:42115397-42115652	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
7	CTCF	chr15:42115400-42115550	Hela-S3	cervix:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
8	CTCF	chr15:42115389-42115645	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
9	CTCF	chr15:42115482-42115565	LNCaP	prostate:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
10	CTCF	chr15:42115446-42115578	GM19239	blood:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
11	CTCF	chr15:42115499-42115584	K562	blood:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
12	CTCF	chr15:42115487-42115579	GM12891	blood:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
13	CTCF	chr15:42115465-42115561	ProgFib	skin:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
14	CTCF	chr15:42115460-42115610	RPTEC	kidney:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
15	CTCF	chr15:42115453-42115599	HepG2	liver:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
16	CTCF	chr15:42115456-42115593	NHEK	skin:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
17	CTCF	chr15:42115460-42115610	BE2_C	brain:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
18	CTCF	chr15:42115437-42115610	Fibrobl	skin:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
19	CTCF	chr15:42115440-42115590	SAEC	small airway:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
20	CTCF	chr15:42115459-42115601	H1-hESC	embryonic stem cell:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
21	CTCF	chr15:42115296-42115722	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
22	CTCF	chr15:42115400-42115550	WERI-Rb-1	eye:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
23	CTCF	chr15:42115408-42115640	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
24	CTCF	chr15:42115460-42115610	HCPEpiC	choroid plexus:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
25	CTCF	chr15:42115480-42115630	WERI-Rb-1	eye:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
26	CTCF	chr15:42115553-42115565	HepG2	liver:	n/a	n/a
27	CTCF	chr15:42115394-42115643	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
28	CTCF	chr15:42115500-42115650	HCT-116	colon:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
29	CTCF	chr15:42115432-42115617	Hela-S3	cervix:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
30	CTCF	chr15:42115395-42115658	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
31	CTCF	chr15:42115431-42115607	Gliobla	brain:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
32	CTCF	chr15:42115420-42115570	HMEC	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
33	CTCF	chr15:42115400-42115550	HBMEC	blood vessel:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
34	CTCF	chr15:42115478-42115570	A549	lung:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
35	CTCF	chr15:42115400-42115550	HepG2	liver:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
36	CTCF	chr15:42115500-42115650	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
37	CTCF	chr15:42115440-42115590	NHEK	skin:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
38	EP300	chr15:42117666-42118614	ECC-1	luminal epithelium:	n/a	n/a
39	ESR1	chr15:42117670-42118420	ECC-1	luminal epithelium:	n/a	n/a
40	ESR1	chr15:42117705-42118411	ECC-1	luminal epithelium:	n/a	n/a
41	HMGN3	chr15:42115683-42115846	K562	blood:	n/a	n/a
42	MYC	chr15:42115390-42115653	MCF-7	breast:	n/a	n/a
43	NFIC	chr15:42117560-42118567	ECC-1	luminal epithelium:	n/a	n/a
44	POLR2A	chr15:42116451-42116993	GM12892	blood:	n/a	n/a
45	POLR2A	chr15:42114217-42114263	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr15:42117004-42117052	HepG2	liver:	n/a	n/a
47	POLR2A	chr15:42116609-42116700	Hela-S3	cervix:	n/a	n/a
48	RAD21	chr15:42115386-42115755	MCF-7	breast:	n/a	chr15:42115525-42115534 chr15:42115524-42115543
49	RAD21	chr15:42115467-42115522	Hela-S3	cervix:	n/a	n/a
50	RAD21	chr15:42115293-42115738	MCF-7	breast:	n/a	chr15:42115525-42115534 chr15:42115524-42115543

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42116798-42116848	HEK293	kidney:	embryo
2	chr15:42116798-42116848	HCF	heart:	n/a
3	chr15:42116798-42116848	HRPEpiC	eye:	n/a
4	chr15:42116798-42116848	HIPEpiC	eye:	n/a
5	chr15:42116798-42116848	PrEC	prostate:	n/a
6	chr15:42116798-42116848	CMK	blood:	n/a
7	chr15:42116798-42116848	MCF10A-Er-Src	breast:	n/a
8	chr15:42116798-42116848	HepG2	liver:	n/a
9	chr15:42116798-42116848	GM06990	blood:	n/a
10	chr15:42116798-42116848	GM12892	blood:	n/a
11	chr15:42116798-42116848	IMR90	lung:	fetal
12	chr15:42116798-42116848	NB4	blood:	n/a
13	chr15:42116798-42116848	Jurkat	blood:	n/a
14	chr15:42116798-42116848	GM19239	blood:	n/a
15	chr15:42116798-42116848	NHDF-neo	bronchial:	n/a
16	chr15:42116798-42116848	ovcar-3	ovarian:	n/a
17	chr15:42116798-42116848	HRE	kidney:	n/a
18	chr15:42116798-42116848	T-47D	breast:	n/a
19	chr15:42116798-42116848	GM12891	blood:	n/a
20	chr15:42116798-42116848	Caco-2	colon:	n/a
21	chr15:42116798-42116848	AG10803	skin:	n/a
22	chr15:42116798-42116848	HCPEpiC	choroid plexus:	n/a
23	chr15:42116798-42116848	HCT-116	colon:	n/a
24	chr15:42116798-42116848	SK-N-SH_RA	brain:	n/a
25	chr15:42116798-42116848	ECC-1	luminal epithelium:	n/a
26	chr15:42116798-42116848	GM12878	blood:	n/a
27	chr15:42116798-42116848	NT2-D1	testis:	n/a
28	chr15:42116798-42116848	NH-A	brain:	n/a
29	chr15:42116798-42116848	HL-60	blood:	n/a
30	chr15:42116798-42116848	MCF-7	breast:	n/a
31	chr15:42116798-42116848	HNPCEpiC	eye:	n/a
32	chr15:42116798-42116848	SAEC	small airway:	n/a
33	chr15:42116798-42116848	HUVEC	blood vessel:	n/a
34	chr15:42116798-42116848	ProgFib	skin:	n/a
35	chr15:42116798-42116848	H1-hESC	embryonic stem cell:	embryo
36	chr15:42116798-42116848	PANC-1	pancreas:	n/a
37	chr15:42116798-42116848	NHBE	bronchial:	n/a
38	chr15:42116798-42116848	HAEpiC	amniotic membrane:	n/a
39	chr15:42116798-42116848	RPTEC	kidney:	n/a
40	chr15:42116798-42116848	HMEC	breast:	n/a
41	chr15:42116798-42116848	AG09309	skin:	n/a
42	chr15:42116798-42116848	AG09319	gingival:	n/a
43	chr15:42116798-42116848	SK-N-MC	brain:	n/a
44	chr15:42116798-42116848	PFSK-1	brain:	n/a
45	chr15:42116798-42116848	SKMC	muscle:	n/a
46	chr15:42116798-42116848	A549	lung:	n/a
47	chr15:42116798-42116848	K562	blood:	n/a
48	chr15:42116798-42116848	BJ	skin:	n/a
49	chr15:42116798-42116848	Hepatocyte	liver:	n/a
50	chr15:42116798-42116848	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:42114563..42118600-chr15:42118704..42121383,3	K562	blood:
2	chr15:41951879..41954479-chr15:42115654..42117641,2	K562	blood:
3	chr15:42114988..42115997-chr15:42196197..42197506,6	MCF-7	breast:
4	chr15:42111390..42114154-chr15:42114914..42116415,2	K562	blood:
5	chr15:42116098..42118578-chr15:42118633..42120214,2	MCF-7	breast:
6	chr15:42115008..42115577-chr15:42196451..42197341,2	MCF-7	breast:
7	chr15:42116882..42118794-chr15:42146288..42147795,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-JMJD7-PLA2G4B-6	chr15:42114848-42115420	NONHSAT041966
2	lnc-JMJD7-PLA2G4B-6	chr15:42115645-42115674	NONHSAT041966
3	lnc-SPTBN5-1	chr15:42117297-42117571	ENSG00000250379.1

Variant related genes	Relation type
PLA2G4B	TF binding region
JMJD7-PLA2G4B	TF binding region
MAPKBP1	TF binding region
JMJD7	TF binding region
PLA2G4B	CpG island
JMJD7-PLA2G4B	CpG island
MAPKBP1	CpG island
JMJD7	CpG island
ENSG00000174197	chromatin interactions
ENSG00000137802	chromatin interactions
ENSG00000168970	chromatin interactions
ENSG00000250379	chromatin interactions
ENSG00000243789	chromatin interactions

Extended variants
information (count: 246 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:246 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556505411	chr15:42113567-42113568	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573323650	chr15:42113573-42113574	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542244660	chr15:42113612-42113613	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559604607	chr15:42113614-42113615	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528825401	chr15:42113649-42113650	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530566387	chr15:42113651-42113652	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs565343412	chr15:42113721-42113722	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530996876	chr15:42113722-42113723	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368467291	chr15:42113727-42113728	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186653403	chr15:42113738-42113739	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200217460	chr15:42113740-42113741	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191883221	chr15:42113742-42113743	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377748398	chr15:42113766-42113767	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs267604191	chr15:42113791-42113792	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs267604192	chr15:42113794-42113795	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs267604193	chr15:42113795-42113796	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201138035	chr15:42113798-42113799	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs199864678	chr15:42113822-42113823	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139818532	chr15:42113874-42113875	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs142058349	chr15:42113884-42113885	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs202085658	chr15:42113888-42113889	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375174822	chr15:42113890-42113891	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369403507	chr15:42113921-42113922	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141865866	chr15:42113922-42113923	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139190271	chr15:42113938-42113939	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149937701	chr15:42113942-42113943	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373392024	chr15:42113960-42113961	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs201550328	chr15:42113975-42113976	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537121387	chr15:42113977-42113978	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369382235	chr15:42113978-42113979	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200595937	chr15:42113983-42113984	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370597630	chr15:42113984-42113985	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs377379452	chr15:42113998-42113999	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528343526	chr15:42114021-42114022	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535836919	chr15:42114026-42114027	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150269120	chr15:42114030-42114031	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138970087	chr15:42114044-42114045	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545389724	chr15:42114096-42114097	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544559537	chr15:42114105-42114106	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs199661010	chr15:42114120-42114121	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs376398422	chr15:42114123-42114124	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs199559079	chr15:42114133-42114134	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200719047	chr15:42114155-42114156	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368170815	chr15:42114156-42114157	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142133358	chr15:42114189-42114190	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184646552	chr15:42114194-42114195	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561350400	chr15:42114198-42114199	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371956245	chr15:42114203-42114204	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376580969	chr15:42114207-42114208	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368689139	chr15:42114215-42114216	Weak transcription Strong transcription Genic 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:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42083800-42119400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:42089400-42114800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr15:42097800-42119600	Weak transcription	Psoas Muscle	Psoas
4	chr15:42098200-42118800	Strong transcription	Fetal Stomach	stomach
5	chr15:42098800-42115600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr15:42100800-42118800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr15:42101800-42119000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr15:42101800-42119600	Weak transcription	Hela-S3	cervix
9	chr15:42102000-42118600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr15:42103200-42118200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr15:42103600-42114000	Strong transcription	Esophagus	oesophagus
12	chr15:42103600-42116600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr15:42103600-42117400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr15:42103600-42118200	Strong transcription	Placenta	Placenta
15	chr15:42103600-42118200	Strong transcription	NHEK	skin
16	chr15:42103600-42118800	Strong transcription	Spleen	Spleen
17	chr15:42103800-42118000	Strong transcription	Brain Anterior Caudate	brain
18	chr15:42103800-42118800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr15:42103800-42118800	Strong transcription	HMEC	breast
20	chr15:42104000-42117000	Weak transcription	Fetal Heart	heart
21	chr15:42104000-42117200	Strong transcription	Brain Angular Gyrus	brain
22	chr15:42104000-42118200	Strong transcription	Stomach Smooth Muscle	stomach
23	chr15:42104000-42118600	Strong transcription	NHLF	lung
24	chr15:42104000-42118800	Strong transcription	Cortex derived primary cultured neurospheres	brain
25	chr15:42104000-42119000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr15:42104000-42119000	Strong transcription	Fetal Muscle Leg	muscle
27	chr15:42104200-42113800	Strong transcription	Dnd41	blood
28	chr15:42104200-42117000	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr15:42104200-42117200	Strong transcription	Adipose Nuclei	Adipose
30	chr15:42104200-42117200	Strong transcription	Brain Cingulate Gyrus	brain
31	chr15:42104200-42117800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr15:42104200-42117800	Strong transcription	Fetal Thymus	thymus
33	chr15:42104200-42117800	Strong transcription	Ovary	ovary
34	chr15:42104200-42117800	Strong transcription	Right Ventricle	heart
35	chr15:42104200-42118200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr15:42104200-42118400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr15:42104200-42118600	Strong transcription	Thymus	Thymus
38	chr15:42104200-42118800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr15:42104200-42118800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr15:42104200-42119400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr15:42104200-42119600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr15:42104200-42119600	Weak transcription	K562	blood
43	chr15:42104400-42114000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr15:42104400-42118600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr15:42104400-42119000	Strong transcription	Fetal Brain Female	brain
46	chr15:42104600-42113600	Strong transcription	HUVEC	blood vessel
47	chr15:42104600-42116200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr15:42104600-42116200	Strong transcription	Left Ventricle	heart
49	chr15:42104600-42116800	Strong transcription	Primary T helper cells fromperipheralblood	blood
50	chr15:42104600-42117400	Strong transcription	Liver	Liver

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