Variant report

Variant	nsv904441
Chromosome Location	chr15:82532963-82580736
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1029)
CpG islands
(count:855)
Chromatin interactive
region (count:20)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1029 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

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	chr15:82579685-82580009	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	ARID3A	chr15:82554834-82555131	HepG2	liver:	n/a	n/a
6	ATF1	chr15:82559461-82559850	K562	blood:	n/a	n/a
7	ATF1	chr15:82579653-82580093	K562	blood:	n/a	n/a
8	ATF1	chr15:82554221-82554539	K562	blood:	n/a	n/a
9	ATF1	chr15:82554940-82555263	K562	blood:	n/a	n/a
10	ATF2	chr15:82578573-82579183	GM12878	blood:	n/a	n/a
11	ATF2	chr15:82579381-82579874	GM12878	blood:	n/a	n/a
12	ATF2	chr15:82578497-82579260	GM12878	blood:	n/a	n/a
13	ATF2	chr15:82554787-82555221	GM12878	blood:	n/a	n/a
14	ATF3	chr15:82554649-82555249	A549	lung:	n/a	n/a
15	BATF	chr15:82578776-82579109	GM12878	blood:	n/a	n/a
16	BATF	chr15:82578722-82579110	GM12878	blood:	n/a	n/a
17	BATF	chr15:82536053-82536235	GM12878	blood:	n/a	n/a
18	BATF	chr15:82579428-82579685	GM12878	blood:	n/a	chr15:82579569-82579580
19	BATF	chr15:82535965-82536263	GM12878	blood:	n/a	n/a
20	BATF	chr15:82578169-82578348	GM12878	blood:	n/a	n/a
21	BATF	chr15:82554283-82554528	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:82578753-82579028	GM12878	blood:	n/a	n/a
23	BCL11A	chr15:82579447-82579672	GM12878	blood:	n/a	n/a
24	BCL11A	chr15:82578726-82579144	GM12878	blood:	n/a	n/a
25	BCL3	chr15:82578562-82579223	GM12878	blood:	n/a	n/a
26	BCL3	chr15:82554620-82555192	A549	lung:	n/a	chr15:82555168-82555176
27	BCLAF1	chr15:82578750-82579243	GM12878	blood:	n/a	n/a
28	BCLAF1	chr15:82554710-82555318	GM12878	blood:	n/a	chr15:82555168-82555176
29	BCLAF1	chr15:82578792-82579220	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:82554471-82555241	GM12878	blood:	n/a	chr15:82554950-82554966 chr15:82554640-82554649 chr15:82554639-82554648 chr15:82554640-82554649 chr15:82554634-82554655
31	BHLHE40	chr15:82554365-82555276	K562	blood:	n/a	chr15:82554950-82554966 chr15:82554640-82554649 chr15:82554639-82554648 chr15:82554640-82554649 chr15:82554634-82554655
32	BHLHE40	chr15:82554476-82555224	HepG2	liver:	n/a	chr15:82554950-82554966 chr15:82554640-82554649 chr15:82554639-82554648 chr15:82554640-82554649 chr15:82554634-82554655
33	BHLHE40	chr15:82578705-82579224	GM12878	blood:	n/a	n/a
34	BRCA1	chr15:82554436-82554804	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr15:82555010-82555075	GM12878	blood:	n/a	n/a
36	BRCA1	chr15:82554360-82555242	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr15:82555006-82555196	HepG2	liver:	n/a	n/a
38	CBX3	chr15:82554755-82555383	K562	blood:	n/a	n/a
39	CCNT2	chr15:82579685-82580075	K562	blood:	n/a	n/a
40	CCNT2	chr15:82559609-82559822	K562	blood:	n/a	n/a
41	CCNT2	chr15:82554793-82555276	K562	blood:	n/a	chr15:82554850-82554859
42	CEBPB	chr15:82554200-82554576	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr15:82554022-82554526	IMR90	lung:	n/a	n/a
44	CEBPB	chr15:82576397-82576587	K562	blood:	n/a	n/a
45	CEBPB	chr15:82556396-82556592	K562	blood:	n/a	chr15:82556467-82556478
46	CEBPB	chr15:82554906-82555291	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr15:82555738-82556072	HepG2	liver:	n/a	n/a
48	CEBPB	chr15:82556432-82556628	HepG2	liver:	n/a	chr15:82556467-82556478
49	CEBPB	chr15:82579879-82580072	K562	blood:	n/a	n/a
50	CEBPD	chr15:82559426-82559961	K562	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:82574624-82574674	GM19239	blood:	n/a
2	chr15:82574624-82574674	GM19239	blood:	n/a
3	chr15:82554820-82554870	HepG2	liver:	n/a
4	chr15:82555456-82555506	HIPEpiC	eye:	n/a
5	chr15:82558555-82558605	SK-N-MC	brain:	n/a
6	chr15:82555552-82555602	AG10803	skin:	n/a
7	chr15:82555390-82555440	GM12892	blood:	n/a
8	chr15:82554902-82554952	AoSMC	blood vessel:	n/a
9	chr15:82558555-82558605	NT2-D1	testis:	n/a
10	chr15:82551086-82551136	AG09309	skin:	n/a
11	chr15:82551086-82551136	AG10803	skin:	n/a
12	chr15:82551086-82551136	MCF-7	breast:	n/a
13	chr15:82553671-82553721	AG04449	skin:	fetal
14	chr15:82553671-82553721	HPAEpiC	pulmonary alveolar:	n/a
15	chr15:82558555-82558605	U87	brain:	n/a
16	chr15:82553671-82553721	GM06990	blood:	n/a
17	chr15:82555552-82555602	GM19239	blood:	n/a
18	chr15:82574624-82574674	HUVEC	blood vessel:	n/a
19	chr15:82555456-82555506	PrEC	prostate:	n/a
20	chr15:82558555-82558605	K562	blood:	n/a
21	chr15:82574624-82574674	HCPEpiC	choroid plexus:	n/a
22	chr15:82554886-82554936	PrEC	prostate:	n/a
23	chr15:82555552-82555602	GM12891	blood:	n/a
24	chr15:82554820-82554870	Jurkat	blood:	n/a
25	chr15:82554886-82554936	Hela-S3	cervix:	n/a
26	chr15:82554886-82554936	U87	brain:	n/a
27	chr15:82554886-82554936	LNCaP	prostate:	n/a
28	chr15:82554820-82554870	HCM	heart:	n/a
29	chr15:82551086-82551136	HRCEpiC	kidney:	n/a
30	chr15:82554902-82554952	HUVEC	blood vessel:	n/a
31	chr15:82555552-82555602	MCF10A-Er-Src	breast:	n/a
32	chr15:82555336-82555386	HepG2	liver:	n/a
33	chr15:82554820-82554870	HRCEpiC	kidney:	n/a
34	chr15:82554820-82554870	NH-A	brain:	n/a
35	chr15:82554886-82554936	HAEpiC	amniotic membrane:	n/a
36	chr15:82555552-82555602	CMK	blood:	n/a
37	chr15:82555113-82555163	A549	lung:	n/a
38	chr15:82555390-82555440	H1-hESC	embryonic stem cell:	embryo
39	chr15:82575848-82575898	HCM	heart:	n/a
40	chr15:82555336-82555386	HRCEpiC	kidney:	n/a
41	chr15:82575848-82575898	Hela-S3	cervix:	n/a
42	chr15:82574624-82574674	Jurkat	blood:	n/a
43	chr15:82554886-82554936	HCPEpiC	choroid plexus:	n/a
44	chr15:82554820-82554870	AG09319	gingival:	n/a
45	chr15:82555456-82555506	GM19239	blood:	n/a
46	chr15:82554584-82554634	Jurkat	blood:	n/a
47	chr15:82574624-82574674	HEK293	kidney:	embryo
48	chr15:82558555-82558605	NHDF-neo	bronchial:	n/a
49	chr15:82551086-82551136	AG04450	lung:	fetal
50	chr15:82554902-82554952	IMR90	lung:	fetal

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

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

(count:3 , 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
3	lnc-GOLGA6L9-5	chr15:82573380-82573998	NONHSAT047774

No data

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

Extended variants
information (count: 1450 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1450 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3759800	chr15:82532963-82532964	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs113213841	chr15:82532987-82532988	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561230134	chr15:82532993-82532994	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144598167	chr15:82533011-82533012	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543826357	chr15:82533037-82533038	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563613130	chr15:82533078-82533079	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532679930	chr15:82533090-82533091	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552492465	chr15:82533191-82533192	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559524772	chr15:82533220-82533221	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12902624	chr15:82533236-82533237	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs145196057	chr15:82533268-82533269	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147488003	chr15:82533310-82533311	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536628578	chr15:82533333-82533334	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139950012	chr15:82533347-82533348	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
15	rs549514327	chr15:82533382-82533383	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142860980	chr15:82533414-82533415	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs151045855	chr15:82533441-82533442	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
18	rs553166951	chr15:82533491-82533492	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139687591	chr15:82533499-82533500	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535716198	chr15:82533585-82533586	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs199762500	chr15:82533590-82533591	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs200705379	chr15:82533597-82533598	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373734975	chr15:82533618-82533619	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs201679284	chr15:82533674-82533675	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201851277	chr15:82533683-82533684	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11548681	chr15:82533686-82533687	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs370998689	chr15:82533698-82533699	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368173835	chr15:82533700-82533701	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs187290995	chr15:82533719-82533720	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140669013	chr15:82533742-82533743	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547321659	chr15:82533779-82533780	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577220512	chr15:82533807-82533808	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs193060238	chr15:82533997-82533998	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs561099764	chr15:82534001-82534002	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72749601	chr15:82534008-82534009	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs141147786	chr15:82534018-82534019	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542053609	chr15:82534062-82534063	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138176100	chr15:82534076-82534077	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs72749602	chr15:82534158-82534159	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs550261804	chr15:82534191-82534192	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375504751	chr15:82534195-82534196	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532856369	chr15:82534248-82534249	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376121607	chr15:82534263-82534264	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79261075	chr15:82534284-82534285	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs62012051	chr15:82534317-82534318	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs189028249	chr15:82534334-82534335	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs193023864	chr15:82534347-82534348	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569052707	chr15:82534405-82534406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538144861	chr15:82534434-82534435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs113439262	chr15:82534446-82534447	Weak transcription Enhancers	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:1249 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

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	chr15:82497600-82536000	Weak transcription	Fetal Heart	heart
5	chr15:82499000-82550800	Weak transcription	HUVEC	blood vessel
6	chr15:82499400-82553000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr15:82501800-82544600	Weak transcription	Brain Angular Gyrus	brain
8	chr15:82503000-82542200	Weak transcription	Stomach Mucosa	stomach
9	chr15:82503200-82552800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr15:82503600-82553000	Weak transcription	Small Intestine	intestine
11	chr15:82503800-82553200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr15:82504200-82553200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr15:82507400-82553000	Weak transcription	NH-A	brain
14	chr15:82508200-82553800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr15:82510800-82554200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr15:82511800-82534800	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr15:82511800-82554200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr15:82512600-82539600	Weak transcription	Spleen	Spleen
19	chr15:82515800-82553600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr15:82520000-82553000	Weak transcription	Gastric	stomach
21	chr15:82520000-82553000	Weak transcription	Right Ventricle	heart
22	chr15:82520000-82553400	Weak transcription	Brain Hippocampus Middle	brain
23	chr15:82520000-82554200	Weak transcription	Pancreas	Pancrea
24	chr15:82520200-82533000	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr15:82520200-82553000	Weak transcription	Psoas Muscle	Psoas
26	chr15:82520200-82554400	Weak transcription	Esophagus	oesophagus
27	chr15:82523000-82550000	Weak transcription	Brain Anterior Caudate	brain
28	chr15:82523600-82553400	Weak transcription	Fetal Kidney	kidney
29	chr15:82524000-82545400	Weak transcription	Fetal Intestine Small	intestine
30	chr15:82524800-82552600	Weak transcription	K562	blood
31	chr15:82527800-82534400	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr15:82528600-82533400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr15:82528600-82534000	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr15:82528800-82533400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr15:82528800-82533800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr15:82529200-82533800	Strong transcription	Thymus	Thymus
37	chr15:82529600-82533000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr15:82529600-82533400	Strong transcription	Adipose Nuclei	Adipose
39	chr15:82529600-82533800	Strong transcription	Fetal Thymus	thymus
40	chr15:82529600-82534400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr15:82529600-82534400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr15:82529600-82534400	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr15:82529800-82533400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr15:82529800-82533400	Strong transcription	Fetal Muscle Leg	muscle
45	chr15:82529800-82533800	Strong transcription	HUES64 Cell Line	embryonic stem cell
46	chr15:82529800-82533800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr15:82530000-82533800	Strong transcription	Liver	Liver
48	chr15:82530000-82534400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr15:82530200-82533200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr15:82530200-82533400	Strong transcription	Primary T helper cells fromperipheralblood	blood

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