Variant report

Variant	nsv1041506
Chromosome Location	chr15:82496164-82581427
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1372)
CpG islands
(count:857)
Chromatin interactive
region (count:26)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1372 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:82524162-82524551	K562	blood:	n/a	n/a
2	ARID3A	chr15:82514032-82514105	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:82555062-82555139	K562	blood:	n/a	n/a
4	ARID3A	chr15:82554834-82555131	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:82555714-82556193	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:82559315-82559851	K562	blood:	n/a	chr15:82559334-82559350
7	ARID3A	chr15:82579685-82580009	K562	blood:	n/a	n/a
8	ATF1	chr15:82531947-82532068	K562	blood:	n/a	n/a
9	ATF1	chr15:82523950-82524615	K562	blood:	n/a	n/a
10	ATF1	chr15:82502554-82502603	K562	blood:	n/a	n/a
11	ATF1	chr15:82554221-82554539	K562	blood:	n/a	n/a
12	ATF1	chr15:82579653-82580093	K562	blood:	n/a	n/a
13	ATF1	chr15:82559461-82559850	K562	blood:	n/a	n/a
14	ATF1	chr15:82554940-82555263	K562	blood:	n/a	n/a
15	ATF2	chr15:82579381-82579874	GM12878	blood:	n/a	n/a
16	ATF2	chr15:82578497-82579260	GM12878	blood:	n/a	n/a
17	ATF2	chr15:82554787-82555221	GM12878	blood:	n/a	n/a
18	ATF2	chr15:82578573-82579183	GM12878	blood:	n/a	n/a
19	ATF3	chr15:82554649-82555249	A549	lung:	n/a	n/a
20	BATF	chr15:82578722-82579110	GM12878	blood:	n/a	n/a
21	BATF	chr15:82578776-82579109	GM12878	blood:	n/a	n/a
22	BATF	chr15:82554283-82554528	GM12878	blood:	n/a	n/a
23	BATF	chr15:82579428-82579685	GM12878	blood:	n/a	chr15:82579569-82579580
24	BATF	chr15:82536053-82536235	GM12878	blood:	n/a	n/a
25	BATF	chr15:82535965-82536263	GM12878	blood:	n/a	n/a
26	BATF	chr15:82578169-82578348	GM12878	blood:	n/a	n/a
27	BCL11A	chr15:82579447-82579672	GM12878	blood:	n/a	n/a
28	BCL11A	chr15:82578726-82579144	GM12878	blood:	n/a	n/a
29	BCL11A	chr15:82578753-82579028	GM12878	blood:	n/a	n/a
30	BCL3	chr15:82554620-82555192	A549	lung:	n/a	chr15:82555168-82555176
31	BCL3	chr15:82578562-82579223	GM12878	blood:	n/a	n/a
32	BCLAF1	chr15:82578750-82579243	GM12878	blood:	n/a	n/a
33	BCLAF1	chr15:82578792-82579220	GM12878	blood:	n/a	n/a
34	BCLAF1	chr15:82554710-82555318	GM12878	blood:	n/a	chr15:82555168-82555176
35	BHLHE40	chr15:82578705-82579224	GM12878	blood:	n/a	n/a
36	BHLHE40	chr15:82554476-82555224	HepG2	liver:	n/a	chr15:82554950-82554966 chr15:82554640-82554649 chr15:82554639-82554648 chr15:82554640-82554649 chr15:82554634-82554655
37	BHLHE40	chr15:82524039-82524518	K562	blood:	n/a	n/a
38	BHLHE40	chr15:82554471-82555241	GM12878	blood:	n/a	chr15:82554950-82554966 chr15:82554640-82554649 chr15:82554639-82554648 chr15:82554640-82554649 chr15:82554634-82554655
39	BHLHE40	chr15:82554365-82555276	K562	blood:	n/a	chr15:82554950-82554966 chr15:82554640-82554649 chr15:82554639-82554648 chr15:82554640-82554649 chr15:82554634-82554655
40	BRCA1	chr15:82555006-82555196	HepG2	liver:	n/a	n/a
41	BRCA1	chr15:82555010-82555075	GM12878	blood:	n/a	n/a
42	BRCA1	chr15:82554360-82555242	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr15:82554436-82554804	H1-hESC	embryonic stem cell:	n/a	n/a
44	CBX3	chr15:82502495-82503014	HCT-116	colon:	n/a	n/a
45	CBX3	chr15:82524106-82524560	K562	blood:	n/a	n/a
46	CBX3	chr15:82554755-82555383	K562	blood:	n/a	n/a
47	CBX3	chr15:82502457-82502885	K562	blood:	n/a	n/a
48	CCNT2	chr15:82559609-82559822	K562	blood:	n/a	n/a
49	CCNT2	chr15:82554793-82555276	K562	blood:	n/a	chr15:82554850-82554859
50	CCNT2	chr15:82579685-82580075	K562	blood:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:82554584-82554634	NH-A	brain:	n/a
2	chr15:82558555-82558605	PANC-1	pancreas:	n/a
3	chr15:82555456-82555506	SAEC	small airway:	n/a
4	chr15:82554584-82554634	NH-A	brain:	n/a
5	chr15:82558555-82558605	PANC-1	pancreas:	n/a
6	chr15:82555456-82555506	SAEC	small airway:	n/a
7	chr15:82558555-82558605	GM06990	blood:	n/a
8	chr15:82555113-82555163	PANC-1	pancreas:	n/a
9	chr15:82555113-82555163	HEEpiC	esophagus:	n/a
10	chr15:82553671-82553721	NHBE	bronchial:	n/a
11	chr15:82555390-82555440	PANC-1	pancreas:	n/a
12	chr15:82555456-82555506	ProgFib	skin:	n/a
13	chr15:82575848-82575898	HCF	heart:	n/a
14	chr15:82575848-82575898	AG10803	skin:	n/a
15	chr15:82553671-82553721	GM06990	blood:	n/a
16	chr15:82554886-82554936	GM12878	blood:	n/a
17	chr15:82575848-82575898	HEEpiC	esophagus:	n/a
18	chr15:82555552-82555602	HCM	heart:	n/a
19	chr15:82555113-82555163	Caco-2	colon:	n/a
20	chr15:82551086-82551136	GM12891	blood:	n/a
21	chr15:82554886-82554936	HNPCEpiC	eye:	n/a
22	chr15:82554584-82554634	AG10803	skin:	n/a
23	chr15:82555456-82555506	AG09319	gingival:	n/a
24	chr15:82555390-82555440	AG04449	skin:	fetal
25	chr15:82554902-82554952	PANC-1	pancreas:	n/a
26	chr15:82558555-82558605	AG10803	skin:	n/a
27	chr15:82554886-82554936	HEEpiC	esophagus:	n/a
28	chr15:82575848-82575898	NB4	blood:	n/a
29	chr15:82574624-82574674	T-47D	breast:	n/a
30	chr15:82555552-82555602	HL-60	blood:	n/a
31	chr15:82554820-82554870	AG04450	lung:	fetal
32	chr15:82555113-82555163	HPAEpiC	pulmonary alveolar:	n/a
33	chr15:82555390-82555440	SK-N-SH_RA	brain:	n/a
34	chr15:82554820-82554870	SK-N-SH_RA	brain:	n/a
35	chr15:82554584-82554634	CMK	blood:	n/a
36	chr15:82551086-82551136	GM12892	blood:	n/a
37	chr15:82554820-82554870	HCT-116	colon:	n/a
38	chr15:82554820-82554870	MCF10A-Er-Src	breast:	n/a
39	chr15:82575848-82575898	T-47D	breast:	n/a
40	chr15:82554886-82554936	U87	brain:	n/a
41	chr15:82551086-82551136	Hepatocyte	liver:	n/a
42	chr15:82555552-82555602	HNPCEpiC	eye:	n/a
43	chr15:82553671-82553721	SK-N-MC	brain:	n/a
44	chr15:82555390-82555440	NHBE	bronchial:	n/a
45	chr15:82554584-82554634	SAEC	small airway:	n/a
46	chr15:82574624-82574674	Hepatocyte	liver:	n/a
47	chr15:82555113-82555163	NHBE	bronchial:	n/a
48	chr15:82553671-82553721	SAEC	small airway:	n/a
49	chr15:82555336-82555386	PANC-1	pancreas:	n/a
50	chr15:82551086-82551136	HCM	heart:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:82544226..82545855-chr15:82550615..82553251,2	K562	blood:
2	chr15:82558957..82560704-chr15:82563268..82565317,2	K562	blood:
3	chr15:82540150..82542827-chr15:82551322..82553905,2	K562	blood:
4	chr15:82558957..82560704-chr15:82563268..82565317,2	K562	blood:
5	chr15:82495558..82497453-chr15:82498796..82500529,2	K562	blood:
6	chr15:82540150..82542827-chr15:82551322..82553905,2	K562	blood:
7	chr15:82524498..82526931-chr15:82528402..82530346,2	MCF-7	breast:
8	chr15:82511968..82514595-chr15:82553137..82554662,2	K562	blood:
9	chr15:82495558..82497453-chr15:82498796..82500529,2	K562	blood:
10	chr15:82514202..82516505-chr15:82518442..82521206,2	K562	blood:
11	chr1:242011083..242011828-chr15:82554163..82555047,2	Hela-S3	cervix:
12	chr12:6862392..6862918-chr15:82554357..82555098,2	Hela-S3	cervix:
13	chr15:82557636..82558140-chr15:84740091..84741075,2	MCF-7	breast:
14	chr15:82550191..82552669-chr15:82553526..82555918,3	MCF-7	breast:
15	chr15:82550051..82552780-chr15:82552889..82555231,4	K562	blood:
16	chr15:82554331..82555047-chr17:39845080..39845674,3	Hela-S3	cervix:
17	chr15:82337966..82340144-chr15:82550811..82553189,2	MCF-7	breast:
18	chr15:82546241..82548403-chr15:82550539..82552952,2	MCF-7	breast:
19	chr15:82556066..82557698-chr15:82564817..82567206,2	MCF-7	breast:
20	chr15:82556066..82557698-chr15:82564817..82567206,2	MCF-7	breast:
21	chr15:82511968..82514595-chr15:82553137..82554662,2	K562	blood:
22	chr15:82554707..82555430-chr17:57915266..57915873,2	MCF-7	breast:
23	chr15:82557073..82558574-chr15:82565794..82567576,2	K562	blood:
24	chr15:82546241..82548403-chr15:82550539..82552952,2	MCF-7	breast:
25	chr15:82514202..82516505-chr15:82518442..82521206,2	K562	blood:
26	chr15:82557073..82558574-chr15:82565794..82567576,2	K562	blood:

(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
FAM154B	TF binding region
EFTUD1	TF binding region
FAM154B	CpG island
EFTUD1	CpG island
ENSG00000183496	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000188659	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000174371	chromatin interactions
ENSG00000140598	chromatin interactions
ENSG00000089693	chromatin interactions

Extended variants
information (count: 2841 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2841 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556179996	chr15:82496199-82496200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs150695380	chr15:82496232-82496233	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538735841	chr15:82496314-82496315	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs71410578	chr15:82496326-82496327	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs185141456	chr15:82496422-82496423	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147921354	chr15:82496503-82496504	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189848335	chr15:82496546-82496547	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574659930	chr15:82496600-82496601	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201686873	chr15:82496629-82496630	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562538195	chr15:82496653-82496654	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531633203	chr15:82496660-82496661	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182567457	chr15:82496662-82496663	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560612882	chr15:82496726-82496727	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565383369	chr15:82496727-82496728	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs34231343	chr15:82496739-82496740	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs115927638	chr15:82496775-82496776	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377461432	chr15:82496803-82496804	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567800266	chr15:82496830-82496831	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536924098	chr15:82496862-82496863	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550543439	chr15:82496889-82496890	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569660336	chr15:82496974-82496975	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538649147	chr15:82496980-82496981	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558339250	chr15:82497028-82497029	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188034671	chr15:82497030-82497031	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11853682	chr15:82497034-82497035	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs145164307	chr15:82497036-82497037	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574590173	chr15:82497058-82497059	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147588679	chr15:82497108-82497109	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556845625	chr15:82497150-82497151	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34300250	chr15:82497153-82497154	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2651697	chr15:82497163-82497164	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545024936	chr15:82497177-82497178	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565202689	chr15:82497180-82497181	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs527773372	chr15:82497182-82497183	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541195756	chr15:82497240-82497241	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142034870	chr15:82497277-82497278	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs151227208	chr15:82497293-82497294	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550458236	chr15:82497308-82497309	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs193076468	chr15:82497337-82497338	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2867622	chr15:82497350-82497351	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140363811	chr15:82497365-82497366	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2651696	chr15:82497400-82497401	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552133220	chr15:82497402-82497403	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183551271	chr15:82497410-82497411	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189043503	chr15:82497411-82497412	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192660468	chr15:82497414-82497415	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2651695	chr15:82497424-82497425	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567872396	chr15:82497464-82497465	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2651694	chr15:82497465-82497466	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2659160	chr15:82497473-82497474	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1970 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:82432600-82552800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr15:82456000-82510000	Weak transcription	Thymus	Thymus
3	chr15:82456400-82502200	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr15:82456400-82502400	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr15:82456400-82502600	Weak transcription	Duodenum Mucosa	Duodenum
6	chr15:82456400-82502800	Weak transcription	Gastric	stomach
7	chr15:82456400-82505400	Weak transcription	Dnd41	blood
8	chr15:82456400-82505600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr15:82456400-82505600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr15:82456600-82497400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr15:82456800-82509800	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr15:82458200-82504800	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr15:82458800-82502800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr15:82462000-82505800	Weak transcription	Primary B cells from cord blood	blood
15	chr15:82465000-82510000	Weak transcription	Placenta	Placenta
16	chr15:82471000-82502200	Weak transcription	NHEK	skin
17	chr15:82471000-82502800	Weak transcription	Fetal Stomach	stomach
18	chr15:82471000-82518600	Weak transcription	Right Ventricle	heart
19	chr15:82474800-82502600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr15:82474800-82502800	Weak transcription	Fetal Intestine Large	intestine
21	chr15:82475400-82502600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr15:82476000-82519200	Weak transcription	Pancreas	Pancrea
23	chr15:82476400-82502800	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr15:82476600-82502400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr15:82477000-82502600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr15:82477000-82510000	Weak transcription	HMEC	breast
27	chr15:82477000-82519200	Weak transcription	HSMMtube	muscle
28	chr15:82477400-82502600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr15:82477600-82522800	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr15:82479600-82496800	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr15:82479800-82510200	Weak transcription	Primary hematopoietic stem cells	blood
32	chr15:82480000-82502800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr15:82481800-82553000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr15:82484800-82502600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr15:82485800-82496800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr15:82485800-82497200	Weak transcription	NHLF	lung
37	chr15:82485800-82502400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr15:82485800-82510000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr15:82485800-82510400	Weak transcription	Osteobl	bone
40	chr15:82486000-82520400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr15:82488000-82519200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr15:82488200-82496600	Weak transcription	Lung	lung
43	chr15:82488200-82510200	Weak transcription	Left Ventricle	heart
44	chr15:82488200-82531200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr15:82488400-82502800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr15:82488600-82502800	Weak transcription	Esophagus	oesophagus
47	chr15:82488600-82505600	Weak transcription	Primary B cells from peripheral blood	blood
48	chr15:82489600-82511400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr15:82490400-82496200	Weak transcription	Fetal Heart	heart
50	chr15:82490400-82502600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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