Variant report

Variant	nsv904443
Chromosome Location	chr15:82553472-82571780
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:657)
CpG islands
(count:671)
Chromatin interactive
region (count:13)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:657 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:82554834-82555131	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:82555062-82555139	K562	blood:	n/a	n/a
3	ARID3A	chr15:82555714-82556193	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:82559315-82559851	K562	blood:	n/a	chr15:82559334-82559350
5	ATF1	chr15:82559461-82559850	K562	blood:	n/a	n/a
6	ATF1	chr15:82554221-82554539	K562	blood:	n/a	n/a
7	ATF1	chr15:82554940-82555263	K562	blood:	n/a	n/a
8	ATF2	chr15:82554787-82555221	GM12878	blood:	n/a	n/a
9	ATF3	chr15:82554649-82555249	A549	lung:	n/a	n/a
10	BATF	chr15:82554283-82554528	GM12878	blood:	n/a	n/a
11	BCL3	chr15:82554620-82555192	A549	lung:	n/a	chr15:82555168-82555176
12	BCLAF1	chr15:82554710-82555318	GM12878	blood:	n/a	chr15:82555168-82555176
13	BHLHE40	chr15:82554476-82555224	HepG2	liver:	n/a	chr15:82554950-82554966 chr15:82554640-82554649 chr15:82554639-82554648 chr15:82554640-82554649 chr15:82554634-82554655
14	BHLHE40	chr15:82554365-82555276	K562	blood:	n/a	chr15:82554950-82554966 chr15:82554640-82554649 chr15:82554639-82554648 chr15:82554640-82554649 chr15:82554634-82554655
15	BHLHE40	chr15:82554471-82555241	GM12878	blood:	n/a	chr15:82554950-82554966 chr15:82554640-82554649 chr15:82554639-82554648 chr15:82554640-82554649 chr15:82554634-82554655
16	BRCA1	chr15:82555006-82555196	HepG2	liver:	n/a	n/a
17	BRCA1	chr15:82554436-82554804	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr15:82555010-82555075	GM12878	blood:	n/a	n/a
19	BRCA1	chr15:82554360-82555242	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr15:82554755-82555383	K562	blood:	n/a	n/a
21	CCNT2	chr15:82559609-82559822	K562	blood:	n/a	n/a
22	CCNT2	chr15:82554793-82555276	K562	blood:	n/a	chr15:82554850-82554859
23	CEBPB	chr15:82556432-82556628	HepG2	liver:	n/a	chr15:82556467-82556478
24	CEBPB	chr15:82555738-82556072	HepG2	liver:	n/a	n/a
25	CEBPB	chr15:82554022-82554526	IMR90	lung:	n/a	n/a
26	CEBPB	chr15:82556396-82556592	K562	blood:	n/a	chr15:82556467-82556478
27	CEBPB	chr15:82554906-82555291	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr15:82554200-82554576	Hela-S3	cervix:	n/a	n/a
29	CEBPD	chr15:82554847-82555176	HepG2	liver:	n/a	n/a
30	CEBPD	chr15:82559426-82559961	K562	blood:	n/a	n/a
31	CHD1	chr15:82554670-82555165	GM12878	blood:	n/a	n/a
32	CHD2	chr15:82554347-82555222	HepG2	liver:	n/a	n/a
33	CHD2	chr15:82554196-82555321	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr15:82554846-82555263	GM12878	blood:	n/a	n/a
35	CHD2	chr15:82554492-82554619	GM12878	blood:	n/a	n/a
36	CHD2	chr15:82554425-82555290	K562	blood:	n/a	n/a
37	CHD2	chr15:82555697-82555999	HepG2	liver:	n/a	n/a
38	CHD2	chr15:82554422-82555298	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr15:82554741-82555422	HepG2	liver:	n/a	n/a
40	CREB1	chr15:82554764-82555383	A549	lung:	n/a	n/a
41	CREB1	chr15:82554785-82555283	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr15:82554765-82555451	GM12878	blood:	n/a	n/a
43	CREB1	chr15:82554854-82555302	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr15:82554879-82555274	A549	lung:	n/a	n/a
45	CTBP2	chr15:82554819-82555280	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr15:82554740-82554890	HCT-116	colon:	n/a	n/a
47	CTCF	chr15:82554432-82554469	GM19239	blood:	n/a	n/a
48	CTCF	chr15:82554389-82554466	GM19238	blood:	n/a	n/a
49	CTCF	chr15:82554960-82555110	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr15:82554410-82554442	GM19240	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:82555336-82555386	NHDF-neo	bronchial:	n/a
2	chr15:82554886-82554936	Hela-S3	cervix:	n/a
3	chr15:82558555-82558605	HRPEpiC	eye:	n/a
4	chr15:82554584-82554634	CMK	blood:	n/a
5	chr15:82555456-82555506	NHBE	bronchial:	n/a
6	chr15:82554820-82554870	PFSK-1	brain:	n/a
7	chr15:82555552-82555602	HRE	kidney:	n/a
8	chr15:82555390-82555440	SK-N-SH	brain:	n/a
9	chr15:82554820-82554870	GM06990	blood:	n/a
10	chr15:82555552-82555602	A549	lung:	n/a
11	chr15:82555336-82555386	H1-hESC	embryonic stem cell:	embryo
12	chr15:82555336-82555386	ECC-1	luminal epithelium:	n/a
13	chr15:82554820-82554870	AG09319	gingival:	n/a
14	chr15:82554902-82554952	AG04450	lung:	fetal
15	chr15:82555336-82555386	GM12878	blood:	n/a
16	chr15:82554584-82554634	BE2_C	brain:	n/a
17	chr15:82554584-82554634	HEEpiC	esophagus:	n/a
18	chr15:82554886-82554936	MCF-7	breast:	n/a
19	chr15:82555552-82555602	H1-hESC	embryonic stem cell:	embryo
20	chr15:82555336-82555386	Hepatocyte	liver:	n/a
21	chr15:82554820-82554870	T-47D	breast:	n/a
22	chr15:82555552-82555602	LNCaP	prostate:	n/a
23	chr15:82555113-82555163	NH-A	brain:	n/a
24	chr15:82558555-82558605	HEEpiC	esophagus:	n/a
25	chr15:82555390-82555440	NH-A	brain:	n/a
26	chr15:82555113-82555163	HCM	heart:	n/a
27	chr15:82555552-82555602	HIPEpiC	eye:	n/a
28	chr15:82554584-82554634	Hepatocyte	liver:	n/a
29	chr15:82554584-82554634	AoSMC	blood vessel:	n/a
30	chr15:82555552-82555602	SAEC	small airway:	n/a
31	chr15:82553671-82553721	HUVEC	blood vessel:	n/a
32	chr15:82555456-82555506	IMR90	lung:	fetal
33	chr15:82553671-82553721	LNCaP	prostate:	n/a
34	chr15:82558555-82558605	PrEC	prostate:	n/a
35	chr15:82554886-82554936	CMK	blood:	n/a
36	chr15:82555336-82555386	A549	lung:	n/a
37	chr15:82555390-82555440	HRE	kidney:	n/a
38	chr15:82554902-82554952	SKMC	muscle:	n/a
39	chr15:82553671-82553721	NT2-D1	testis:	n/a
40	chr15:82555390-82555440	T-47D	breast:	n/a
41	chr15:82553671-82553721	H1-hESC	embryonic stem cell:	embryo
42	chr15:82554886-82554936	HEK293	kidney:	embryo
43	chr15:82555390-82555440	AG10803	skin:	n/a
44	chr15:82555552-82555602	PFSK-1	brain:	n/a
45	chr15:82558555-82558605	PFSK-1	brain:	n/a
46	chr15:82555552-82555602	HAEpiC	amniotic membrane:	n/a
47	chr15:82558555-82558605	SK-N-SH_RA	brain:	n/a
48	chr15:82553671-82553721	GM12878	blood:	n/a
49	chr15:82555456-82555506	HepG2	liver:	n/a
50	chr15:82555456-82555506	HRCEpiC	kidney:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:82556066..82557698-chr15:82564817..82567206,2	MCF-7	breast:
2	chr12:6862392..6862918-chr15:82554357..82555098,2	Hela-S3	cervix:
3	chr15:82556066..82557698-chr15:82564817..82567206,2	MCF-7	breast:
4	chr15:82558957..82560704-chr15:82563268..82565317,2	K562	blood:
5	chr15:82511968..82514595-chr15:82553137..82554662,2	K562	blood:
6	chr1:242011083..242011828-chr15:82554163..82555047,2	Hela-S3	cervix:
7	chr15:82557073..82558574-chr15:82565794..82567576,2	K562	blood:
8	chr15:82557636..82558140-chr15:84740091..84741075,2	MCF-7	breast:
9	chr15:82554331..82555047-chr17:39845080..39845674,3	Hela-S3	cervix:
10	chr15:82558957..82560704-chr15:82563268..82565317,2	K562	blood:
11	chr15:82540150..82542827-chr15:82551322..82553905,2	K562	blood:
12	chr15:82554707..82555430-chr17:57915266..57915873,2	MCF-7	breast:
13	chr15:82557073..82558574-chr15:82565794..82567576,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLGA6L9-6	chr15:82555485-82555529	NONHSAT047773
2	lnc-GOLGA6L9-6	chr15:82557014-82557230	NONHSAT047773

No data

Variant related genes	Relation type
FAM154B	TF binding region
EFTUD1	TF binding region
FAM154B	CpG island
EFTUD1	CpG island
ENSG00000062716	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000174371	chromatin interactions
ENSG00000089693	chromatin interactions

Extended variants
information (count: 567 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1501366	chr15:82553472-82553473	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs373521342	chr15:82553489-82553490	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs115183249	chr15:82553507-82553508	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs538695224	chr15:82553530-82553531	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs576102813	chr15:82553538-82553539	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs559003362	chr15:82553550-82553551	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs181686838	chr15:82553556-82553557	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs67461403	chr15:82553560-82553561	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs541185868	chr15:82553598-82553599	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs117084180	chr15:82553667-82553668	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs185109629	chr15:82553671-82553672	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs573799535	chr15:82553753-82553754	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs190011167	chr15:82553755-82553756	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs28660473	chr15:82553773-82553774	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs142340329	chr15:82553834-82553835	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs2867648	chr15:82553948-82553949	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs146905221	chr15:82553972-82553973	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551933884	chr15:82553977-82553978	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs376786372	chr15:82553985-82553986	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs369213314	chr15:82553999-82554000	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs373675663	chr15:82554020-82554021	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs200183257	chr15:82554023-82554024	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs370108445	chr15:82554031-82554032	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs528186412	chr15:82554151-82554152	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs548372923	chr15:82554171-82554172	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs568286006	chr15:82554181-82554182	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs537275227	chr15:82554183-82554184	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs550882532	chr15:82554184-82554185	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs570700745	chr15:82554197-82554198	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs182283769	chr15:82554199-82554200	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs3032079	chr15:82554205-82554206	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs558690348	chr15:82554217-82554218	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs201167991	chr15:82554226-82554227	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs139302502	chr15:82554246-82554247	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs534813347	chr15:82554261-82554262	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs140557826	chr15:82554323-82554324	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs114006250	chr15:82554377-82554378	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs543650244	chr15:82554385-82554386	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs557629965	chr15:82554386-82554387	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs3973875	chr15:82554388-82554389	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs545745091	chr15:82554431-82554432	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs150447925	chr15:82554508-82554509	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs528167479	chr15:82554522-82554523	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs186493183	chr15:82554566-82554567	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs561804966	chr15:82554622-82554623	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs561271266	chr15:82554625-82554626	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs2867649	chr15:82554672-82554673	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs138259166	chr15:82554712-82554713	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs79531287	chr15:82554758-82554759	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs570685600	chr15:82554795-82554796	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Congenital diaphragmatic hernia	20921022	CNVD
abnormal development	18461090	CNVD
Intellectual disability	22102821	CNVD
renal disease	17924346	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:651 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:82497000-82553600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr15:82508200-82553800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr15:82510800-82554200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr15:82511800-82554200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr15:82515800-82553600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr15:82520000-82554200	Weak transcription	Pancreas	Pancrea
7	chr15:82520200-82554400	Weak transcription	Esophagus	oesophagus
8	chr15:82532000-82554000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr15:82533200-82553600	Weak transcription	Fetal Lung	lung
10	chr15:82533400-82553800	Weak transcription	Aorta	Aorta
11	chr15:82533400-82553800	Weak transcription	Brain Substantia Nigra	brain
12	chr15:82533400-82554000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr15:82533400-82554200	Weak transcription	Colonic Mucosa	Colon
14	chr15:82533800-82554200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr15:82537000-82554200	Weak transcription	Ovary	ovary
16	chr15:82538200-82554400	Weak transcription	Lung	lung
17	chr15:82541000-82554400	Weak transcription	Spleen	Spleen
18	chr15:82544800-82554000	Weak transcription	Brain Angular Gyrus	brain
19	chr15:82545600-82554000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr15:82545800-82553800	Weak transcription	Fetal Stomach	stomach
21	chr15:82545800-82554200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr15:82547000-82554400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr15:82549800-82553800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr15:82551200-82553800	Weak transcription	Stomach Smooth Muscle	stomach
25	chr15:82551200-82554000	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr15:82551200-82554200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr15:82551400-82553800	Weak transcription	Adipose Nuclei	Adipose
28	chr15:82551400-82553800	Weak transcription	Liver	Liver
29	chr15:82551400-82554000	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr15:82551400-82554000	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr15:82551400-82554200	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr15:82551400-82554200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr15:82551400-82554200	Weak transcription	Fetal Muscle Trunk	muscle
34	chr15:82551400-82554200	Weak transcription	Placenta	Placenta
35	chr15:82551600-82553800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr15:82551600-82554200	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr15:82551600-82554200	Weak transcription	Brain Anterior Caudate	brain
38	chr15:82551600-82554200	Weak transcription	Fetal Muscle Leg	muscle
39	chr15:82551800-82554000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr15:82552200-82553800	Enhancers	Fetal Brain Male	brain
41	chr15:82552400-82553600	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr15:82552400-82556800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr15:82552600-82554200	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr15:82552800-82553600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
45	chr15:82552800-82553600	Transcr. at gene 5' and 3'	Dnd41	blood
46	chr15:82552800-82553600	Flanking Active TSS	K562	blood
47	chr15:82552800-82553800	Enhancers	Primary T cells from cord blood	blood
48	chr15:82552800-82553800	Enhancers	Fetal Intestine Small	intestine
49	chr15:82552800-82554000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr15:82552800-82554000	Enhancers	HepG2	liver

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