Variant report

Variant	nsv904442
Chromosome Location	chr15:82540174-82571046
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:686)
CpG islands
(count:735)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:686 , 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	chr15:82555062-82555139	K562	blood:	n/a	n/a
2	ARID3A	chr15:82559315-82559851	K562	blood:	n/a	chr15:82559334-82559350
3	ARID3A	chr15:82554834-82555131	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:82555714-82556193	HepG2	liver:	n/a	n/a
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	chr15:82554365-82555276	K562	blood:	n/a	chr15:82554950-82554966 chr15:82554640-82554649 chr15:82554639-82554648 chr15:82554640-82554649 chr15:82554634-82554655
14	BHLHE40	chr15:82554476-82555224	HepG2	liver:	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	chr15:82555010-82555075	GM12878	blood:	n/a	n/a
18	BRCA1	chr15:82554360-82555242	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr15:82554436-82554804	H1-hESC	embryonic stem cell:	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	chr15:82555738-82556072	HepG2	liver:	n/a	n/a
24	CEBPB	chr15:82556432-82556628	HepG2	liver:	n/a	chr15:82556467-82556478
25	CEBPB	chr15:82554906-82555291	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr15:82554200-82554576	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr15:82556396-82556592	K562	blood:	n/a	chr15:82556467-82556478
28	CEBPB	chr15:82554022-82554526	IMR90	lung:	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	chr15:82554196-82555321	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr15:82554492-82554619	GM12878	blood:	n/a	n/a
34	CHD2	chr15:82555697-82555999	HepG2	liver:	n/a	n/a
35	CHD2	chr15:82554347-82555222	HepG2	liver:	n/a	n/a
36	CHD2	chr15:82554846-82555263	GM12878	blood:	n/a	n/a
37	CHD2	chr15:82554425-82555290	K562	blood:	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	chr15:82554785-82555283	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr15:82554764-82555383	A549	lung:	n/a	n/a
42	CREB1	chr15:82554854-82555302	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr15:82554765-82555451	GM12878	blood:	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	chr15:82554900-82555050	AG04449	skin:	n/a	n/a
47	CTCF	chr15:82554280-82554430	HMEC	breast:	n/a	n/a
48	CTCF	chr15:82554349-82554534	Gliobla	brain:	n/a	n/a
49	CTCF	chr15:82554365-82554466	MCF-7	breast:	n/a	n/a
50	CTCF	chr15:82554410-82554442	GM19240	blood:	n/a	n/a

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:82555336-82555386	K562	blood:	n/a
2	chr15:82555113-82555163	HAEpiC	amniotic membrane:	n/a
3	chr15:82554886-82554936	HCM	heart:	n/a
4	chr15:82555336-82555386	K562	blood:	n/a
5	chr15:82555113-82555163	HAEpiC	amniotic membrane:	n/a
6	chr15:82554886-82554936	HCM	heart:	n/a
7	chr15:82554886-82554936	Hepatocyte	liver:	n/a
8	chr15:82554584-82554634	ovcar-3	ovarian:	n/a
9	chr15:82551086-82551136	AoSMC	blood vessel:	n/a
10	chr15:82555113-82555163	AG04449	skin:	fetal
11	chr15:82554584-82554634	LNCaP	prostate:	n/a
12	chr15:82554902-82554952	HEEpiC	esophagus:	n/a
13	chr15:82554886-82554936	HPAEpiC	pulmonary alveolar:	n/a
14	chr15:82555552-82555602	HCT-116	colon:	n/a
15	chr15:82558555-82558605	MCF10A-Er-Src	breast:	n/a
16	chr15:82554584-82554634	SK-N-SH_RA	brain:	n/a
17	chr15:82551086-82551136	CMK	blood:	n/a
18	chr15:82558555-82558605	GM19239	blood:	n/a
19	chr15:82554584-82554634	AG10803	skin:	n/a
20	chr15:82555390-82555440	BE2_C	brain:	n/a
21	chr15:82555456-82555506	HEK293	kidney:	embryo
22	chr15:82551086-82551136	HMEC	breast:	n/a
23	chr15:82555390-82555440	SAEC	small airway:	n/a
24	chr15:82554820-82554870	HRCEpiC	kidney:	n/a
25	chr15:82555336-82555386	IMR90	lung:	fetal
26	chr15:82554820-82554870	K562	blood:	n/a
27	chr15:82555456-82555506	HepG2	liver:	n/a
28	chr15:82555456-82555506	HCF	heart:	n/a
29	chr15:82555113-82555163	SK-N-SH	brain:	n/a
30	chr15:82553671-82553721	A549	lung:	n/a
31	chr15:82551086-82551136	AG09319	gingival:	n/a
32	chr15:82554820-82554870	RPTEC	kidney:	n/a
33	chr15:82558555-82558605	HEEpiC	esophagus:	n/a
34	chr15:82553671-82553721	SK-N-SH_RA	brain:	n/a
35	chr15:82554584-82554634	HCT-116	colon:	n/a
36	chr15:82551086-82551136	MCF10A-Er-Src	breast:	n/a
37	chr15:82555113-82555163	A549	lung:	n/a
38	chr15:82555456-82555506	NHBE	bronchial:	n/a
39	chr15:82551086-82551136	NHBE	bronchial:	n/a
40	chr15:82554886-82554936	BE2_C	brain:	n/a
41	chr15:82554820-82554870	HCPEpiC	choroid plexus:	n/a
42	chr15:82555336-82555386	HUVEC	blood vessel:	n/a
43	chr15:82555336-82555386	GM12878	blood:	n/a
44	chr15:82555552-82555602	AoSMC	blood vessel:	n/a
45	chr15:82555336-82555386	LNCaP	prostate:	n/a
46	chr15:82551086-82551136	GM19239	blood:	n/a
47	chr15:82555552-82555602	A549	lung:	n/a
48	chr15:82554584-82554634	AG09319	gingival:	n/a
49	chr15:82554584-82554634	Jurkat	blood:	n/a
50	chr15:82555113-82555163	LNCaP	prostate:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:82557073..82558574-chr15:82565794..82567576,2	K562	blood:
2	chr15:82558957..82560704-chr15:82563268..82565317,2	K562	blood:
3	chr12:6862392..6862918-chr15:82554357..82555098,2	Hela-S3	cervix:
4	chr15:82556066..82557698-chr15:82564817..82567206,2	MCF-7	breast:
5	chr15:82544226..82545855-chr15:82550615..82553251,2	K562	blood:
6	chr15:82337966..82340144-chr15:82550811..82553189,2	MCF-7	breast:
7	chr15:82540150..82542827-chr15:82551322..82553905,2	K562	blood:
8	chr15:82556066..82557698-chr15:82564817..82567206,2	MCF-7	breast:
9	chr15:82540150..82542827-chr15:82551322..82553905,2	K562	blood:
10	chr15:82550191..82552669-chr15:82553526..82555918,3	MCF-7	breast:
11	chr15:82546241..82548403-chr15:82550539..82552952,2	MCF-7	breast:
12	chr1:242011083..242011828-chr15:82554163..82555047,2	Hela-S3	cervix:
13	chr15:82554331..82555047-chr17:39845080..39845674,3	Hela-S3	cervix:
14	chr15:82511968..82514595-chr15:82553137..82554662,2	K562	blood:
15	chr15:82546241..82548403-chr15:82550539..82552952,2	MCF-7	breast:
16	chr15:82550051..82552780-chr15:82552889..82555231,4	K562	blood:
17	chr15:82554707..82555430-chr17:57915266..57915873,2	MCF-7	breast:
18	chr15:82557073..82558574-chr15:82565794..82567576,2	K562	blood:
19	chr15:82557636..82558140-chr15:84740091..84741075,2	MCF-7	breast:
20	chr15:82558957..82560704-chr15:82563268..82565317,2	K562	blood:

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

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

No data

Variant related genes	Relation type
EFTUD1	TF binding region
FAM154B	TF binding region
EFTUD1	CpG island
FAM154B	CpG island
ENSG00000173812	chromatin interactions
ENSG00000188659	chromatin interactions
ENSG00000174371	chromatin interactions
ENSG00000089693	chromatin interactions
ENSG00000140598	chromatin interactions
ENSG00000183496	chromatin interactions
ENSG00000062716	chromatin interactions

Extended variants
information (count: 1020 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1020 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8028284	chr15:82540174-82540175	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374585555	chr15:82540241-82540242	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149846466	chr15:82540242-82540243	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553248849	chr15:82540278-82540279	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs4778988	chr15:82540337-82540338	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs567902306	chr15:82540338-82540339	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4778673	chr15:82540411-82540412	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs192531028	chr15:82540431-82540432	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574800453	chr15:82540472-82540473	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537925281	chr15:82540475-82540476	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370701430	chr15:82540481-82540482	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546123278	chr15:82540487-82540488	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557021531	chr15:82540503-82540504	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148558290	chr15:82540524-82540525	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564418639	chr15:82540542-82540543	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545984103	chr15:82540658-82540659	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs34471747	chr15:82540673-82540674	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs528745347	chr15:82540683-82540684	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373642136	chr15:82540691-82540692	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542531100	chr15:82540699-82540700	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368106759	chr15:82540735-82540736	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562270373	chr15:82540784-82540785	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532027082	chr15:82540799-82540800	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs151227378	chr15:82540817-82540818	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550119216	chr15:82540909-82540910	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35786339	chr15:82540970-82540971	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs371571736	chr15:82541003-82541004	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150371984	chr15:82541111-82541112	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529766040	chr15:82541150-82541151	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75304191	chr15:82541211-82541212	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533060705	chr15:82541297-82541298	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184967712	chr15:82541318-82541319	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs61277938	chr15:82541348-82541349	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs199550834	chr15:82541365-82541366	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374772898	chr15:82541368-82541369	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546780447	chr15:82541398-82541399	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369763573	chr15:82541399-82541400	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189843453	chr15:82541421-82541422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535361650	chr15:82541456-82541457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566690475	chr15:82541464-82541465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138056274	chr15:82541466-82541467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569093249	chr15:82541472-82541473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117443990	chr15:82541499-82541500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181702862	chr15:82541505-82541506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576880115	chr15:82541514-82541515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539559990	chr15:82541517-82541518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553123156	chr15:82541547-82541548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184812173	chr15:82541549-82541550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573362851	chr15:82541575-82541576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542091622	chr15:82541584-82541585	Weak transcription Strong transcription	n/a	n/a	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:1021 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:82432600-82552800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr15:82481800-82553000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr15:82497000-82553600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr15:82499000-82550800	Weak transcription	HUVEC	blood vessel
5	chr15:82499400-82553000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr15:82501800-82544600	Weak transcription	Brain Angular Gyrus	brain
7	chr15:82503000-82542200	Weak transcription	Stomach Mucosa	stomach
8	chr15:82503200-82552800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr15:82503600-82553000	Weak transcription	Small Intestine	intestine
10	chr15:82503800-82553200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr15:82504200-82553200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr15:82507400-82553000	Weak transcription	NH-A	brain
13	chr15:82508200-82553800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr15:82510800-82554200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr15:82511800-82554200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr15:82515800-82553600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr15:82520000-82553000	Weak transcription	Gastric	stomach
18	chr15:82520000-82553000	Weak transcription	Right Ventricle	heart
19	chr15:82520000-82553400	Weak transcription	Brain Hippocampus Middle	brain
20	chr15:82520000-82554200	Weak transcription	Pancreas	Pancrea
21	chr15:82520200-82553000	Weak transcription	Psoas Muscle	Psoas
22	chr15:82520200-82554400	Weak transcription	Esophagus	oesophagus
23	chr15:82523000-82550000	Weak transcription	Brain Anterior Caudate	brain
24	chr15:82523600-82553400	Weak transcription	Fetal Kidney	kidney
25	chr15:82524000-82545400	Weak transcription	Fetal Intestine Small	intestine
26	chr15:82524800-82552600	Weak transcription	K562	blood
27	chr15:82531800-82543200	Weak transcription	Fetal Stomach	stomach
28	chr15:82532000-82554000	Weak transcription	Brain Cingulate Gyrus	brain
29	chr15:82532400-82549800	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr15:82532600-82543600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr15:82532600-82550600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr15:82532600-82552800	Weak transcription	Fetal Brain Female	brain
33	chr15:82532600-82553400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr15:82532800-82550400	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr15:82532800-82550600	Weak transcription	Stomach Smooth Muscle	stomach
36	chr15:82533000-82543200	Weak transcription	Placenta	Placenta
37	chr15:82533000-82544400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr15:82533000-82553000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr15:82533000-82553400	Weak transcription	Colon Smooth Muscle	Colon
40	chr15:82533200-82540800	Weak transcription	NHDF-Ad	bronchial
41	chr15:82533200-82545600	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr15:82533200-82545600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr15:82533200-82550800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr15:82533200-82552200	Weak transcription	Fetal Brain Male	brain
45	chr15:82533200-82553000	Weak transcription	NHLF	lung
46	chr15:82533200-82553200	Weak transcription	Brain Germinal Matrix	brain
47	chr15:82533200-82553200	Weak transcription	A549	lung
48	chr15:82533200-82553600	Weak transcription	Fetal Lung	lung
49	chr15:82533400-82543000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr15:82533400-82544600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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