Variant report

Variant	nsv569906
Chromosome Location	chr15:72126034-72218036
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:416)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:72212595-72212649	K562	blood:	n/a	n/a
2	ARID3A	chr15:72213921-72213933	K562	blood:	n/a	n/a
3	ATF2	chr15:72206368-72206921	GM12878	blood:	n/a	n/a
4	BATF	chr15:72206431-72206854	GM12878	blood:	n/a	chr15:72206656-72206667
5	BATF	chr15:72172137-72172404	GM12878	blood:	n/a	n/a
6	BATF	chr15:72166614-72167024	GM12878	blood:	n/a	n/a
7	BATF	chr15:72206435-72206822	GM12878	blood:	n/a	chr15:72206656-72206667
8	BATF	chr15:72172158-72172394	GM12878	blood:	n/a	n/a
9	BCL11A	chr15:72206377-72206869	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:72206400-72206839	GM12878	blood:	n/a	n/a
11	BCL3	chr15:72206413-72206809	GM12878	blood:	n/a	n/a
12	BHLHE40	chr15:72168244-72168288	GM12878	blood:	n/a	n/a
13	BHLHE40	chr15:72183574-72183575	K562	blood:	n/a	n/a
14	BHLHE40	chr15:72166665-72166809	GM12878	blood:	n/a	n/a
15	CEBPB	chr15:72179288-72179290	A549	lung:	n/a	n/a
16	CEBPB	chr15:72157924-72158099	K562	blood:	n/a	n/a
17	CEBPB	chr15:72132445-72132548	HepG2	liver:	n/a	n/a
18	CEBPB	chr15:72142970-72143097	HepG2	liver:	n/a	chr15:72143057-72143068
19	CEBPB	chr15:72142982-72143174	HepG2	liver:	n/a	chr15:72143057-72143068
20	CEBPB	chr15:72142997-72143098	K562	blood:	n/a	chr15:72143057-72143068
21	CEBPB	chr15:72142902-72143176	H1-hESC	embryonic stem cell:	n/a	chr15:72143057-72143068
22	CEBPB	chr15:72144375-72144640	HepG2	liver:	n/a	n/a
23	CEBPB	chr15:72142983-72143105	IMR90	lung:	n/a	chr15:72143057-72143068
24	CEBPB	chr15:72142899-72143104	A549	lung:	n/a	chr15:72143057-72143068
25	CHD1	chr15:72166676-72166792	GM12878	blood:	n/a	n/a
26	CTCF	chr15:72142972-72143738	A549	lung:	n/a	n/a
27	CTCF	chr15:72143280-72143430	HCFaa	heart:	n/a	n/a
28	CTCF	chr15:72134040-72134190	MCF-7	breast:	n/a	n/a
29	CTCF	chr15:72143280-72143430	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr15:72143300-72143450	GM12875	blood:	n/a	n/a
31	CTCF	chr15:72143320-72143470	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr15:72143263-72143430	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr15:72134032-72134153	MCF-7	breast:	n/a	n/a
34	CTCF	chr15:72143260-72143410	K562	blood:	n/a	n/a
35	CTCF	chr15:72143280-72143430	Caco-2	colon:	n/a	n/a
36	CTCF	chr15:72143352-72143409	GM12892	blood:	n/a	n/a
37	CTCF	chr15:72143200-72143350	WI-38	lung:	n/a	n/a
38	CTCF	chr15:72143290-72143473	A549	lung:	n/a	n/a
39	CTCF	chr15:72143260-72143410	SAEC	small airway:	n/a	n/a
40	CTCF	chr15:72134120-72134270	HCT-116	colon:	n/a	n/a
41	CTCF	chr15:72143300-72143450	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr15:72143280-72143430	GM12874	blood:	n/a	n/a
43	CTCF	chr15:72143261-72143471	LNCaP	prostate:	n/a	n/a
44	CTCF	chr15:72143320-72143470	AG09309	skin:	n/a	n/a
45	CTCF	chr15:72143200-72143350	GM12878	blood:	n/a	n/a
46	CTCF	chr15:72143300-72143450	HPF	lung:	n/a	n/a
47	CTCF	chr15:72143300-72143450	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr15:72192683-72192728	GM13977	blood:	n/a	n/a
49	CTCF	chr15:72143300-72143450	BE2_C	brain:	n/a	n/a
50	CTCF	chr15:72143620-72143770	HPF	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:72178118-72178168	HUVEC	blood vessel:	n/a
2	chr15:72178118-72178168	HRE	kidney:	n/a
3	chr15:72178118-72178168	NT2-D1	testis:	n/a
4	chr15:72178118-72178168	HNPCEpiC	eye:	n/a
5	chr15:72178118-72178168	HL-60	blood:	n/a
6	chr15:72178118-72178168	HEK293	kidney:	embryo
7	chr15:72178118-72178168	MCF-7	breast:	n/a
8	chr15:72178118-72178168	GM12892	blood:	n/a
9	chr15:72178118-72178168	Hepatocyte	liver:	n/a
10	chr15:72178118-72178168	HPAEpiC	pulmonary alveolar:	n/a
11	chr15:72178118-72178168	MCF10A-Er-Src	breast:	n/a
12	chr15:72178118-72178168	GM19239	blood:	n/a
13	chr15:72178118-72178168	PFSK-1	brain:	n/a
14	chr15:72178118-72178168	HCT-116	colon:	n/a
15	chr15:72178118-72178168	IMR90	lung:	fetal
16	chr15:72178118-72178168	AG04449	skin:	fetal
17	chr15:72178118-72178168	HAEpiC	amniotic membrane:	n/a
18	chr15:72178118-72178168	PrEC	prostate:	n/a
19	chr15:72178118-72178168	HCPEpiC	choroid plexus:	n/a
20	chr15:72178118-72178168	GM12878	blood:	n/a
21	chr15:72178118-72178168	SAEC	small airway:	n/a
22	chr15:72178118-72178168	HCF	heart:	n/a
23	chr15:72178118-72178168	Hela-S3	cervix:	n/a
24	chr15:72178118-72178168	LNCaP	prostate:	n/a
25	chr15:72178118-72178168	RPTEC	kidney:	n/a
26	chr15:72178118-72178168	HRPEpiC	eye:	n/a
27	chr15:72178118-72178168	Jurkat	blood:	n/a
28	chr15:72178118-72178168	Caco-2	colon:	n/a
29	chr15:72178118-72178168	SKMC	muscle:	n/a
30	chr15:72178118-72178168	GM06990	blood:	n/a
31	chr15:72178118-72178168	SK-N-SH_RA	brain:	n/a
32	chr15:72178118-72178168	SK-N-MC	brain:	n/a
33	chr15:72178118-72178168	T-47D	breast:	n/a
34	chr15:72178118-72178168	GM12891	blood:	n/a
35	chr15:72178118-72178168	NHDF-neo	bronchial:	n/a
36	chr15:72178118-72178168	BJ	skin:	n/a
37	chr15:72178118-72178168	AG09309	skin:	n/a
38	chr15:72178118-72178168	HCM	heart:	n/a
39	chr15:72178118-72178168	SK-N-SH	brain:	n/a
40	chr15:72178118-72178168	AG09319	gingival:	n/a
41	chr15:72178118-72178168	HepG2	liver:	n/a
42	chr15:72178118-72178168	HIPEpiC	eye:	n/a
43	chr15:72178118-72178168	A549	lung:	n/a
44	chr15:72178118-72178168	U87	brain:	n/a
45	chr15:72178118-72178168	NH-A	brain:	n/a
46	chr15:72178118-72178168	HMEC	breast:	n/a
47	chr15:72178118-72178168	AG04450	lung:	fetal
48	chr15:72178118-72178168	AoSMC	blood vessel:	n/a
49	chr15:72178118-72178168	PANC-1	pancreas:	n/a
50	chr15:72178118-72178168	HRCEpiC	kidney:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:72138309..72141068-chr15:72175580..72177408,2	MCF-7	breast:
2	chr15:72183241..72185017-chr15:72188166..72190098,2	MCF-7	breast:
3	chr15:72114514..72117570-chr15:72121768..72126233,5	K562	blood:
4	chr15:72187197..72189830-chr15:72197152..72199761,2	K562	blood:
5	chr15:72197435..72199145-chr15:72206196..72207927,2	K562	blood:
6	chr15:72180763..72183209-chr15:72189285..72191973,2	MCF-7	breast:
7	chr15:72183241..72185017-chr15:72188166..72190098,2	MCF-7	breast:
8	chr15:72204090..72205988-chr15:72208798..72210918,2	K562	blood:
9	chr15:72197435..72199145-chr15:72206196..72207927,2	K562	blood:
10	chr15:72132772..72134478-chr15:72147156..72150104,2	MCF-7	breast:
11	chr15:72114725..72116485-chr15:72127394..72129983,2	MCF-7	breast:
12	chr15:72168681..72170784-chr15:72179926..72181699,2	MCF-7	breast:
13	chr15:72137846..72140290-chr15:72140971..72143287,2	K562	blood:
14	chr15:72143069..72145942-chr15:72153528..72155127,2	K562	blood:
15	chr15:72138309..72141068-chr15:72175580..72177408,2	MCF-7	breast:
16	chr15:72176973..72179854-chr15:72407858..72409826,2	MCF-7	breast:
17	chr15:72173982..72176259-chr15:72181202..72184060,3	K562	blood:
18	chr15:72137846..72140290-chr15:72140971..72143287,2	K562	blood:
19	chr15:72180763..72183209-chr15:72189285..72191973,2	MCF-7	breast:
20	chr15:72177869..72180074-chr15:72180572..72182469,2	MCF-7	breast:
21	chr15:72187197..72189830-chr15:72197152..72199761,2	K562	blood:
22	chr15:72132772..72134478-chr15:72147156..72150104,2	MCF-7	breast:
23	chr15:72190232..72191910-chr15:72203994..72206448,2	MCF-7	breast:
24	chr15:72204090..72205988-chr15:72208798..72210918,2	K562	blood:
25	chr15:72173982..72176259-chr15:72181202..72184060,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THSD4-6	chr15:72132953-72133522	l_1185_chr15:72128517-72133047_colon
2	lnc-THSD4-6	chr15:72128518-72129537	l_1185_chr15:72128517-72133047_colon
3	lnc-GRAMD2-4	chr15:72189802-72190154	NONHSAT047057
4	lnc-GRAMD2-4	chr15:72185803-72186119	NONHSAT047057

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MYO9A	hsa-let-7c-5p	chr15:72183618-72183640

Variant related genes	Relation type
RNA5SP399	TF binding region
MYO9A	TF binding region
RNA5SP399	CpG island
MYO9A	CpG island
ENSG00000066933	chromatin interactions
ENSG00000166192	chromatin interactions

Extended variants
information (count: 3092 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3092 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2625530	chr15:72126034-72126035	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556437758	chr15:72126067-72126068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373805319	chr15:72126094-72126095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549597234	chr15:72126174-72126175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200959521	chr15:72126254-72126255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577911302	chr15:72126297-72126298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189754402	chr15:72126359-72126360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560154618	chr15:72126370-72126371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527773221	chr15:72126377-72126378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532621705	chr15:72126607-72126608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561305931	chr15:72126632-72126633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375682426	chr15:72126782-72126783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12592401	chr15:72126793-72126794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576333189	chr15:72126801-72126802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183016786	chr15:72126852-72126853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115687952	chr15:72126859-72126860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs34754556	chr15:72126864-72126865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138125666	chr15:72126876-72126877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551389925	chr15:72126885-72126886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113334528	chr15:72126887-72126888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528666742	chr15:72126947-72126948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566520161	chr15:72127001-72127002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533851637	chr15:72127044-72127045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187586490	chr15:72127154-72127155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192969376	chr15:72127187-72127188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538046242	chr15:72127203-72127204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556141946	chr15:72127249-72127250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs79435784	chr15:72127258-72127259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565430573	chr15:72127267-72127268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184607546	chr15:72127268-72127269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544949107	chr15:72127273-72127274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553724891	chr15:72127314-72127315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572138773	chr15:72127358-72127359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2625531	chr15:72127364-72127365	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs149521013	chr15:72127369-72127370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531767412	chr15:72127383-72127384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544005676	chr15:72127388-72127389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12909770	chr15:72127407-72127408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12908450	chr15:72127408-72127409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374275700	chr15:72127455-72127456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143997418	chr15:72127566-72127567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35614030	chr15:72127587-72127588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532855751	chr15:72127738-72127739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548137527	chr15:72127739-72127740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560176844	chr15:72127749-72127750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527301702	chr15:72127771-72127772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549072661	chr15:72127794-72127795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567362611	chr15:72127804-72127805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537581324	chr15:72127805-72127806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142099078	chr15:72127880-72127881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	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
Lung cancer	18438408	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
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
Autism	20678247	CNVD
Retinoblastoma	21504564	CNVD
Matthew-Wood syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Urothelial cell carcinoma	18451213	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Mental retardation	17621639	CNVD
Autism	20808228	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	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
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1634 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72114600-72190600	Weak transcription	Pancreas	Pancrea
2	chr15:72115800-72147000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr15:72116000-72140800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr15:72116000-72142000	Weak transcription	Hela-S3	cervix
5	chr15:72116400-72147000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr15:72117000-72142800	Weak transcription	Stomach Mucosa	stomach
7	chr15:72118800-72131400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr15:72119200-72171800	Weak transcription	Psoas Muscle	Psoas
9	chr15:72119400-72130200	Weak transcription	HUVEC	blood vessel
10	chr15:72119400-72142400	Weak transcription	Fetal Thymus	thymus
11	chr15:72119600-72139000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr15:72119800-72140800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr15:72119800-72142200	Weak transcription	Spleen	Spleen
14	chr15:72120200-72138400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr15:72120200-72139000	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr15:72120400-72131400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr15:72120400-72138600	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr15:72120400-72142400	Weak transcription	GM12878-XiMat	blood
19	chr15:72120600-72139800	Weak transcription	HMEC	breast
20	chr15:72120600-72147400	Weak transcription	Small Intestine	intestine
21	chr15:72120800-72142200	Weak transcription	Colonic Mucosa	Colon
22	chr15:72122200-72138400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr15:72122200-72139000	Weak transcription	Fetal Brain Male	brain
24	chr15:72122200-72189400	Weak transcription	Right Ventricle	heart
25	chr15:72122400-72131000	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr15:72122400-72136000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr15:72122400-72136000	Weak transcription	HSMMtube	muscle
28	chr15:72122400-72137200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr15:72122400-72137400	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr15:72122400-72139200	Weak transcription	Fetal Brain Female	brain
31	chr15:72122400-72140200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr15:72122400-72141800	Weak transcription	NH-A	brain
33	chr15:72122400-72142200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr15:72122400-72195000	Weak transcription	NHEK	skin
35	chr15:72122600-72128000	Weak transcription	Colon Smooth Muscle	Colon
36	chr15:72122600-72130800	Weak transcription	Primary T cells from cord blood	blood
37	chr15:72122600-72131400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr15:72122600-72131400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr15:72122600-72131600	Weak transcription	Adipose Nuclei	Adipose
40	chr15:72122600-72131800	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr15:72122600-72132400	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr15:72122600-72132600	Weak transcription	Left Ventricle	heart
43	chr15:72122600-72133200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr15:72122600-72134800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr15:72122600-72135200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr15:72122600-72135200	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr15:72122600-72135400	Weak transcription	Fetal Intestine Small	intestine
48	chr15:72122600-72135600	Weak transcription	Brain Germinal Matrix	brain
49	chr15:72122600-72136000	Weak transcription	Liver	Liver
50	chr15:72122600-72136800	Weak transcription	Monocytes-CD14+_RO01746	blood

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