Variant report

Variant	nsv974601
Chromosome Location	chr15:76139204-76160467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:127)
CpG islands
(count:63)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:127 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76156863-76157147	K562	blood:	n/a	n/a
2	ATF1	chr15:76155259-76155429	K562	blood:	n/a	n/a
3	ATF1	chr15:76148791-76148912	K562	blood:	n/a	n/a
4	ATF3	chr15:76156853-76157104	K562	blood:	n/a	n/a
5	BACH1	chr15:76139988-76140006	K562	blood:	n/a	n/a
6	BHLHE40	chr15:76156671-76156811	K562	blood:	n/a	n/a
7	BHLHE40	chr15:76157609-76157689	K562	blood:	n/a	n/a
8	CEBPB	chr15:76156753-76157196	K562	blood:	n/a	n/a
9	CEBPB	chr15:76156856-76157187	K562	blood:	n/a	n/a
10	CEBPB	chr15:76140340-76140526	K562	blood:	n/a	n/a
11	CEBPB	chr15:76156849-76157176	A549	lung:	n/a	n/a
12	CEBPB	chr15:76156820-76157355	IMR90	lung:	n/a	n/a
13	CEBPB	chr15:76156822-76157130	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr15:76156775-76157399	K562	blood:	n/a	n/a
15	CEBPB	chr15:76156825-76157180	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr15:76154283-76154347	IMR90	lung:	n/a	n/a
17	CREB1	chr15:76159655-76160102	GM12878	blood:	n/a	n/a
18	CTCF	chr15:76148456-76148530	Lung_OC	lung:	n/a	n/a
19	CTCF	chr15:76159968-76160050	GM20000	blood:	n/a	n/a
20	CTCF	chr15:76149857-76149878	GM20000	blood:	n/a	n/a
21	CTCF	chr15:76141304-76141355	GM13976	blood:	n/a	n/a
22	CTCF	chr15:76160360-76160510	GM12873	blood:	n/a	n/a
23	CUX1	chr15:76141527-76141688	K562	blood:	n/a	n/a
24	CUX1	chr15:76159868-76160068	GM12878	blood:	n/a	n/a
25	CUX1	chr15:76139838-76139954	GM12878	blood:	n/a	n/a
26	CUX1	chr15:76156704-76157071	K562	blood:	n/a	n/a
27	E2F4	chr15:76146275-76146537	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F6	chr15:76146399-76146509	K562	blood:	n/a	n/a
29	E2F6	chr15:76146295-76146624	H1-hESC	embryonic stem cell:	n/a	n/a
30	E2F6	chr15:76146220-76146645	H1-hESC	embryonic stem cell:	n/a	n/a
31	EBF1	chr15:76143529-76143596	GM12878	blood:	n/a	chr15:76143558-76143569
32	EP300	chr15:76155074-76155458	T-47D	breast:	n/a	n/a
33	EP300	chr15:76144972-76145009	GM12878	blood:	n/a	n/a
34	EP300	chr15:76156563-76157361	K562	blood:	n/a	chr15:76156992-76157006 chr15:76156950-76156964 chr15:76156951-76156965 chr15:76156949-76156963
35	EP300	chr15:76140306-76140398	GM12878	blood:	n/a	chr15:76140370-76140384 chr15:76140371-76140380
36	EP300	chr15:76141535-76141965	K562	blood:	n/a	chr15:76141704-76141718
37	FOS	chr15:76146285-76146485	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr15:76146396-76146482	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr15:76146322-76146492	MCF10A-Er-Src	breast:	n/a	n/a
40	FOXA1	chr15:76155183-76155613	T-47D	breast:	n/a	n/a
41	GATA1	chr15:76142403-76142933	PBDEFetal	blood:	n/a	n/a
42	GATA2	chr15:76155163-76155433	SH-SY5Y	brain:	n/a	chr15:76155277-76155284 chr15:76155277-76155286 chr15:76155270-76155291 chr15:76155277-76155284 chr15:76155278-76155295 chr15:76155277-76155284
43	GATA3	chr15:76155171-76155577	MCF-7	breast:	n/a	chr15:76155277-76155284 chr15:76155277-76155286 chr15:76155270-76155291 chr15:76155276-76155284 chr15:76155277-76155284 chr15:76155278-76155295 chr15:76155277-76155284
44	GATA3	chr15:76155157-76155638	MCF-7	breast:	n/a	chr15:76155277-76155284 chr15:76155277-76155286 chr15:76155270-76155291 chr15:76155276-76155284 chr15:76155277-76155284 chr15:76155278-76155295 chr15:76155277-76155284
45	GATA3	chr15:76150174-76150569	SK-N-SH	brain:	n/a	n/a
46	GATA3	chr15:76149504-76149681	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr15:76155583-76155729	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr15:76150184-76150537	MCF-7	breast:	n/a	n/a
49	GATA3	chr15:76155091-76155547	T-47D	breast:	n/a	chr15:76155277-76155284 chr15:76155277-76155286 chr15:76155270-76155291 chr15:76155276-76155284 chr15:76155277-76155284 chr15:76155278-76155295 chr15:76155277-76155284
50	GATA3	chr15:76139554-76139630	SH-SY5Y	brain:	n/a	n/a

(count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76159937-76159987	RPTEC	kidney:	n/a
2	chr15:76159937-76159987	SKMC	muscle:	n/a
3	chr15:76159937-76159987	RPTEC	kidney:	n/a
4	chr15:76159937-76159987	SKMC	muscle:	n/a
5	chr15:76159937-76159987	Hela-S3	cervix:	n/a
6	chr15:76159937-76159987	ECC-1	luminal epithelium:	n/a
7	chr15:76159937-76159987	Jurkat	blood:	n/a
8	chr15:76159937-76159987	AG09319	gingival:	n/a
9	chr15:76159937-76159987	NHDF-neo	bronchial:	n/a
10	chr15:76159937-76159987	SK-N-MC	brain:	n/a
11	chr15:76159937-76159987	HEK293	kidney:	embryo
12	chr15:76159937-76159987	HCM	heart:	n/a
13	chr15:76159937-76159987	BE2_C	brain:	n/a
14	chr15:76159937-76159987	HMEC	breast:	n/a
15	chr15:76159937-76159987	NH-A	brain:	n/a
16	chr15:76159937-76159987	A549	lung:	n/a
17	chr15:76159937-76159987	NB4	blood:	n/a
18	chr15:76159937-76159987	PANC-1	pancreas:	n/a
19	chr15:76159937-76159987	GM19239	blood:	n/a
20	chr15:76159937-76159987	HUVEC	blood vessel:	n/a
21	chr15:76159937-76159987	U87	brain:	n/a
22	chr15:76159937-76159987	NT2-D1	testis:	n/a
23	chr15:76159937-76159987	HRPEpiC	eye:	n/a
24	chr15:76159937-76159987	HAEpiC	amniotic membrane:	n/a
25	chr15:76159937-76159987	AG10803	skin:	n/a
26	chr15:76159937-76159987	SAEC	small airway:	n/a
27	chr15:76159937-76159987	GM06990	blood:	n/a
28	chr15:76159937-76159987	HL-60	blood:	n/a
29	chr15:76159937-76159987	AG04449	skin:	fetal
30	chr15:76159937-76159987	HCT-116	colon:	n/a
31	chr15:76159937-76159987	HPAEpiC	pulmonary alveolar:	n/a
32	chr15:76159937-76159987	GM12878	blood:	n/a
33	chr15:76159937-76159987	T-47D	breast:	n/a
34	chr15:76159937-76159987	HCF	heart:	n/a
35	chr15:76159937-76159987	Hepatocyte	liver:	n/a
36	chr15:76159937-76159987	HRE	kidney:	n/a
37	chr15:76159937-76159987	PFSK-1	brain:	n/a
38	chr15:76159937-76159987	NHBE	bronchial:	n/a
39	chr15:76159937-76159987	SK-N-SH_RA	brain:	n/a
40	chr15:76159937-76159987	H1-hESC	embryonic stem cell:	embryo
41	chr15:76159937-76159987	IMR90	lung:	fetal
42	chr15:76159937-76159987	ProgFib	skin:	n/a
43	chr15:76159937-76159987	HNPCEpiC	eye:	n/a
44	chr15:76159937-76159987	HCPEpiC	choroid plexus:	n/a
45	chr15:76159937-76159987	AG09309	skin:	n/a
46	chr15:76159937-76159987	PrEC	prostate:	n/a
47	chr15:76159937-76159987	MCF-7	breast:	n/a
48	chr15:76159937-76159987	SK-N-SH	brain:	n/a
49	chr15:76159937-76159987	MCF10A-Er-Src	breast:	n/a
50	chr15:76159937-76159987	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:76136933..76140770-chr15:76154598..76157335,3	K562	blood:
2	chr15:76135011..76136849-chr15:76154600..76156725,2	K562	blood:
3	chr15:52310337..52312699-chr15:76160460..76162429,2	MCF-7	breast:
4	chr15:76150916..76153778-chr15:76157480..76159086,2	K562	blood:
5	chr15:76146991..76149009-chr15:76171055..76173285,2	MCF-7	breast:
6	chr15:76133681..76139746-chr15:76193985..76199740,23	MCF-7	breast:
7	chr15:76140669..76144139-chr15:76145486..76148047,3	MCF-7	breast:
8	chr15:76134659..76136703-chr15:76156027..76158190,3	MCF-7	breast:
9	chr15:76151970..76153778-chr15:76157385..76159086,2	K562	blood:
10	chr15:76134343..76136099-chr15:76152538..76154299,2	MCF-7	breast:
11	chr15:76135173..76137779-chr15:76157818..76161014,3	K562	blood:
12	chr15:76137352..76139853-chr15:76196046..76197847,3	MCF-7	breast:
13	chr15:76145771..76148111-chr15:76152063..76154131,2	MCF-7	breast:
14	chr15:76140669..76144139-chr15:76145486..76148047,3	MCF-7	breast:
15	chr15:76145071..76146601-chr15:76196281..76198612,2	K562	blood:
16	chr15:76154276..76157270-chr15:76157615..76160562,3	K562	blood:
17	chr15:76133451..76137775-chr15:76156108..76161375,6	MCF-7	breast:
18	chr15:76136933..76140770-chr15:76154598..76157335,3	K562	blood:
19	chr15:76134245..76136824-chr15:76150305..76152111,2	MCF-7	breast:
20	chr15:76156695..76159097-chr15:76174173..76176640,2	K562	blood:
21	chr15:76136467..76138938-chr15:76146625..76148978,2	MCF-7	breast:
22	chr15:76154276..76157270-chr15:76157615..76160562,3	K562	blood:
23	chr15:76157186..76158925-chr15:76160347..76162015,2	MCF-7	breast:
24	chr15:76135872..76137923-chr15:76143662..76145313,3	MCF-7	breast:

No data

Variant related genes	Relation type
UBE2Q2	TF binding region
UBE2Q2	CpG island
ENSG00000167196	chromatin interactions
ENSG00000140367	chromatin interactions
ENSG00000069956	chromatin interactions
ENSG00000259438	chromatin interactions

Extended variants
information (count: 756 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:756 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549773327	chr15:76139219-76139220	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs556816506	chr15:76139414-76139415	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs199957708	chr15:76139473-76139474	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs2593300	chr15:76139534-76139535	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs546065014	chr15:76139624-76139625	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs150350007	chr15:76139708-76139709	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs528351985	chr15:76139739-76139740	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs138064160	chr15:76139741-76139742	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs559671564	chr15:76139743-76139744	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs538741130	chr15:76139838-76139839	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs575122535	chr15:76139848-76139849	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs530891262	chr15:76139930-76139931	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs532137836	chr15:76139964-76139965	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs530067962	chr15:76139991-76139992	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs570216309	chr15:76140002-76140003	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs548645986	chr15:76140021-76140022	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs142705825	chr15:76140027-76140028	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs530915350	chr15:76140055-76140056	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs552312995	chr15:76140079-76140080	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs71403520	chr15:76140080-76140081	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs182642413	chr15:76140148-76140149	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs188904140	chr15:76140155-76140156	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs536592218	chr15:76140186-76140187	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs8041834	chr15:76140197-76140198	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs535148191	chr15:76140220-76140221	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs557014366	chr15:76140236-76140237	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs575361667	chr15:76140262-76140263	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs138245278	chr15:76140297-76140298	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs557947306	chr15:76140344-76140345	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs1699270	chr15:76140356-76140357	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs1799634	chr15:76140372-76140373	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs142839755	chr15:76140391-76140392	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs34177262	chr15:76140401-76140402	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs35571341	chr15:76140406-76140407	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs376318944	chr15:76140414-76140415	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs540498135	chr15:76140424-76140425	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs1699269	chr15:76140441-76140442	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs193102995	chr15:76140446-76140447	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs367556226	chr15:76140449-76140450	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs28550045	chr15:76140486-76140487	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs1618530	chr15:76140489-76140490	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs541813519	chr15:76140512-76140513	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs146082062	chr15:76140513-76140514	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs530879358	chr15:76140611-76140612	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs183036099	chr15:76140640-76140641	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs564321620	chr15:76140642-76140643	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs528698733	chr15:76140676-76140677	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs187660368	chr15:76140689-76140690	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs148749625	chr15:76140695-76140696	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs12909182	chr15:76140860-76140861	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
XY gonadal dysgenesis	20685758	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76134800-76140400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr15:76137000-76139400	Enhancers	Sigmoid Colon	Sigmoid Colon
3	chr15:76137000-76139800	Transcr. at gene 5' and 3'	K562	blood
4	chr15:76137200-76139400	Enhancers	Primary B cells from peripheral blood	blood
5	chr15:76137200-76140800	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr15:76137200-76166200	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr15:76137400-76139400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr15:76137400-76139400	Enhancers	Placenta	Placenta
9	chr15:76137400-76140000	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr15:76137600-76139400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr15:76137600-76141400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr15:76137600-76141600	Enhancers	Fetal Heart	heart
13	chr15:76137600-76147000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr15:76137600-76147600	Weak transcription	Fetal Intestine Small	intestine
15	chr15:76137600-76155400	Weak transcription	Stomach Mucosa	stomach
16	chr15:76137600-76165000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr15:76137800-76140400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr15:76137800-76140400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr15:76137800-76143000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr15:76137800-76152400	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr15:76137800-76165800	Weak transcription	Liver	Liver
22	chr15:76137800-76166000	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr15:76137800-76188400	Weak transcription	Brain Anterior Caudate	brain
24	chr15:76138000-76139400	Enhancers	Primary T cells fromperipheralblood	blood
25	chr15:76138000-76139400	Enhancers	Fetal Thymus	thymus
26	chr15:76138000-76139800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr15:76138000-76140000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr15:76138000-76140000	Enhancers	Fetal Brain Male	brain
29	chr15:76138000-76140000	Enhancers	HepG2	liver
30	chr15:76138000-76141200	Enhancers	Fetal Lung	lung
31	chr15:76138000-76141400	Enhancers	Primary T cells from cord blood	blood
32	chr15:76138000-76146000	Weak transcription	Right Ventricle	heart
33	chr15:76138000-76146800	Weak transcription	Osteobl	bone
34	chr15:76138000-76151000	Weak transcription	Primary B cells from cord blood	blood
35	chr15:76138000-76179600	Weak transcription	Small Intestine	intestine
36	chr15:76138200-76139400	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr15:76138200-76139400	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr15:76138200-76139600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr15:76138200-76139600	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr15:76138200-76139800	Enhancers	HMEC	breast
41	chr15:76138200-76140000	Enhancers	NHEK	skin
42	chr15:76138200-76140600	Weak transcription	Colonic Mucosa	Colon
43	chr15:76138200-76141000	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr15:76138200-76141800	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr15:76138200-76141800	Weak transcription	Ovary	ovary
46	chr15:76138200-76142200	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr15:76138200-76142200	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr15:76138200-76143600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr15:76138200-76143600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr15:76138200-76145200	Enhancers	Primary T helper cells PMA-I stimulated	--

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