Variant report

Variant	nsv615640
Chromosome Location	chr9:136515297-136528721
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:305)
Chromatin interactive
region (count:19)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:161 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:136523744-136523833	HepG2	liver:	n/a	n/a
2	BACH1	chr9:136523856-136524290	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr9:136522095-136522108	HepG2	liver:	n/a	n/a
4	CEBPB	chr9:136523948-136524147	HepG2	liver:	n/a	chr9:136524109-136524120
5	CEBPB	chr9:136524014-136524140	Hela-S3	cervix:	n/a	chr9:136524109-136524120
6	CEBPD	chr9:136523381-136524320	HepG2	liver:	n/a	n/a
7	CHD2	chr9:136523633-136523998	HepG2	liver:	n/a	n/a
8	CHD2	chr9:136523850-136524056	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr9:136521700-136521850	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr9:136522540-136522712	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr9:136521652-136521882	HepG2	liver:	n/a	n/a
12	CTCF	chr9:136521642-136521910	T-47D	breast:	n/a	n/a
13	CTCF	chr9:136521736-136521776	GM12892	blood:	n/a	n/a
14	CTCF	chr9:136521739-136521834	Spleen_OC	spleen:	n/a	n/a
15	CTCF	chr9:136521736-136521809	Lung_OC	lung:	n/a	n/a
16	CTCF	chr9:136521731-136521806	MCF-7	breast:	n/a	n/a
17	CTCF	chr9:136521660-136521810	HepG2	liver:	n/a	n/a
18	CTCF	chr9:136522530-136522680	Lung_OC	lung:	n/a	n/a
19	CTCF	chr9:136521701-136521816	MCF-7	breast:	n/a	n/a
20	CTCF	chr9:136521724-136521806	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr9:136521720-136521870	HMEC	breast:	n/a	n/a
22	CTCF	chr9:136521702-136521828	NHEK	skin:	n/a	n/a
23	CTCF	chr9:136523000-136523150	BE2_C	brain:	n/a	n/a
24	CTCF	chr9:136521715-136521827	MCF-7	breast:	n/a	n/a
25	CTCF	chr9:136522578-136522713	Fibrobl	skin:	n/a	n/a
26	E2F4	chr9:136523839-136524011	MCF10A-Er-Src	breast:	n/a	n/a
27	EGR1	chr9:136523725-136524293	ECC-1	luminal epithelium:	n/a	n/a
28	EGR1	chr9:136523698-136524280	MCF-7	breast:	n/a	n/a
29	EGR1	chr9:136523733-136524228	ECC-1	luminal epithelium:	n/a	n/a
30	EGR1	chr9:136523810-136524119	K562	blood:	n/a	n/a
31	EGR1	chr9:136523524-136524350	HCT-116	colon:	n/a	n/a
32	EGR1	chr9:136523812-136524171	K562	blood:	n/a	n/a
33	EGR1	chr9:136523524-136524381	HCT-116	colon:	n/a	n/a
34	ELF1	chr9:136523657-136524019	HepG2	liver:	n/a	n/a
35	ELF1	chr9:136523782-136524015	K562	blood:	n/a	n/a
36	EP300	chr9:136523551-136524071	HepG2	liver:	n/a	n/a
37	EP300	chr9:136523720-136523920	HepG2	liver:	n/a	n/a
38	EP300	chr9:136523614-136524420	ECC-1	luminal epithelium:	n/a	n/a
39	FOSL2	chr9:136522577-136525475	HepG2	liver:	n/a	n/a
40	FOXA1	chr9:136523855-136524200	T-47D	breast:	n/a	n/a
41	FOXA1	chr9:136523478-136524230	HepG2	liver:	n/a	n/a
42	FOXA1	chr9:136523454-136524302	HepG2	liver:	n/a	n/a
43	FOXA1	chr9:136523484-136524060	HepG2	liver:	n/a	n/a
44	FOXA1	chr9:136523512-136524024	HepG2	liver:	n/a	n/a
45	FOXA1	chr9:136523936-136524170	ECC-1	luminal epithelium:	n/a	n/a
46	FOXA2	chr9:136523592-136523935	HepG2	liver:	n/a	n/a
47	FOXA2	chr9:136523950-136524272	HepG2	liver:	n/a	n/a
48	HA-E2F1	chr9:136523786-136524505	MCF-7	breast:	n/a	n/a
49	HDAC2	chr9:136523505-136524177	HepG2	liver:	n/a	n/a
50	HNF4A	chr9:136523488-136524054	HepG2	liver:	n/a	chr9:136523853-136523868

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:136522927-136522977	AG04450	lung:	fetal
2	chr9:136522716-136522766	SK-N-SH	brain:	n/a
3	chr9:136516616-136516666	HNPCEpiC	eye:	n/a
4	chr9:136520852-136520902	HUVEC	blood vessel:	n/a
5	chr9:136522662-136522712	GM12891	blood:	n/a
6	chr9:136520852-136520902	GM12878	blood:	n/a
7	chr9:136522662-136522712	HAEpiC	amniotic membrane:	n/a
8	chr9:136522716-136522766	T-47D	breast:	n/a
9	chr9:136520852-136520902	AG10803	skin:	n/a
10	chr9:136522662-136522712	LNCaP	prostate:	n/a
11	chr9:136520852-136520902	HRCEpiC	kidney:	n/a
12	chr9:136522662-136522712	IMR90	lung:	fetal
13	chr9:136522716-136522766	SK-N-SH_RA	brain:	n/a
14	chr9:136516616-136516666	SK-N-MC	brain:	n/a
15	chr9:136522662-136522712	PrEC	prostate:	n/a
16	chr9:136520852-136520902	CMK	blood:	n/a
17	chr9:136516616-136516666	GM19239	blood:	n/a
18	chr9:136520852-136520902	A549	lung:	n/a
19	chr9:136520852-136520902	LNCaP	prostate:	n/a
20	chr9:136520852-136520902	GM06990	blood:	n/a
21	chr9:136522662-136522712	ProgFib	skin:	n/a
22	chr9:136522662-136522712	HCF	heart:	n/a
23	chr9:136522662-136522712	BJ	skin:	n/a
24	chr9:136522716-136522766	HRE	kidney:	n/a
25	chr9:136520852-136520902	SKMC	muscle:	n/a
26	chr9:136522662-136522712	AoSMC	blood vessel:	n/a
27	chr9:136522927-136522977	HEEpiC	esophagus:	n/a
28	chr9:136522662-136522712	ovcar-3	ovarian:	n/a
29	chr9:136522716-136522766	HRCEpiC	kidney:	n/a
30	chr9:136520852-136520902	Hela-S3	cervix:	n/a
31	chr9:136522927-136522977	SAEC	small airway:	n/a
32	chr9:136522927-136522977	GM12878	blood:	n/a
33	chr9:136522927-136522977	MCF10A-Er-Src	breast:	n/a
34	chr9:136522662-136522712	HEEpiC	esophagus:	n/a
35	chr9:136522662-136522712	GM19239	blood:	n/a
36	chr9:136522716-136522766	Hepatocyte	liver:	n/a
37	chr9:136516616-136516666	HEK293	kidney:	embryo
38	chr9:136522662-136522712	HCT-116	colon:	n/a
39	chr9:136522716-136522766	BE2_C	brain:	n/a
40	chr9:136520852-136520902	HMEC	breast:	n/a
41	chr9:136522662-136522712	BE2_C	brain:	n/a
42	chr9:136522927-136522977	Jurkat	blood:	n/a
43	chr9:136516616-136516666	AG04450	lung:	fetal
44	chr9:136522927-136522977	H1-hESC	embryonic stem cell:	embryo
45	chr9:136522662-136522712	T-47D	breast:	n/a
46	chr9:136516616-136516666	AG09319	gingival:	n/a
47	chr9:136522927-136522977	AG10803	skin:	n/a
48	chr9:136522716-136522766	ProgFib	skin:	n/a
49	chr9:136522716-136522766	SAEC	small airway:	n/a
50	chr9:136522927-136522977	T-47D	breast:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:136523144..136526065-chr9:136527921..136530216,2	MCF-7	breast:
2	chr9:136397976..136398826-chr9:136528405..136529390,2	MCF-7	breast:
3	chr9:136528532..136530062-chr9:136535645..136537164,2	K562	blood:
4	chr9:136514740..136517614-chr9:136519360..136521535,2	K562	blood:
5	chr9:136492846..136495441-chr9:136522709..136525633,2	MCF-7	breast:
6	chr9:136528562..136531390-chr9:136533335..136537164,3	K562	blood:
7	chr9:136514740..136517614-chr9:136519360..136521535,2	K562	blood:
8	chr9:136508750..136511596-chr9:136514989..136519879,4	K562	blood:
9	chr9:136406344..136408415-chr9:136524304..136526688,2	MCF-7	breast:
10	chr9:136521310..136521871-chr9:136591160..136591908,2	MCF-7	breast:
11	chr9:136523144..136526065-chr9:136527921..136530216,2	MCF-7	breast:
12	chr9:136518974..136520647-chr9:136523004..136525968,2	K562	blood:
13	chr9:136518974..136520647-chr9:136523004..136525968,2	K562	blood:
14	chr9:136524956..136527895-chr9:136529322..136531931,3	MCF-7	breast:
15	chr9:136514960..136517246-chr9:136545398..136548011,2	K562	blood:
16	chr9:136518974..136521399-chr9:136523004..136525968,3	K562	blood:
17	chr9:136518974..136521399-chr9:136523004..136525968,3	K562	blood:
18	chr9:136520134..136522462-chr9:136523738..136526239,2	MCF-7	breast:
19	chr9:136528592..136530737-chr9:136533318..136534835,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SARDH-1	chr9:136522249-136522530	NR_102735
2	lnc-SARDH-1	chr9:136519708-136521659	ENSG00000225756.1
3	lnc-SARDH-1	chr9:136519708-136522571	NONHSAT135334
4	lnc-SARDH-1	chr9:136522249-136524916	NONHSAT135333
5	lnc-SARDH-1	chr9:136522249-136522435	ENSG00000225756.1
6	lnc-SARDH-1	chr9:136519317-136521659	NONHSAT135333
7	lnc-SARDH-1	chr9:136519709-136521659	NR_102735
8	lnc-SARDH-1	chr9:136522216-136525145	NONHSAT135332
9	lnc-SARDH-1	chr9:136519271-136521659	NONHSAT135332
10	lnc-SARDH-1	chr9:136522611-136522653	NONHSAT135334

No data

Variant related genes	Relation type
DBH-AS1	TF binding region
DBH-AS1	CpG island
ENSG00000225756	chromatin interactions

Extended variants
information (count: 817 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2283123	chr9:136515297-136515298	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572237350	chr9:136515324-136515325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2283124	chr9:136515330-136515331	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs564150239	chr9:136515339-136515340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78106270	chr9:136515394-136515395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561477589	chr9:136515458-136515459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543045096	chr9:136515493-136515494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561675430	chr9:136515549-136515550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs72088880	chr9:136515554-136515555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs59837456	chr9:136515555-136515556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs59091279	chr9:136515564-136515565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140359937	chr9:136515568-136515569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72293809	chr9:136515575-136515576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs61629543	chr9:136515580-136515581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200207629	chr9:136515581-136515582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540002449	chr9:136515586-136515587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146236948	chr9:136515589-136515590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548033594	chr9:136515596-136515597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs60456420	chr9:136515597-136515598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs71981752	chr9:136515603-136515604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs57809088	chr9:136515607-136515608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199903357	chr9:136515608-136515609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559640464	chr9:136515612-136515613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533327038	chr9:136515613-136515614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551592780	chr9:136515622-136515623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569805712	chr9:136515625-136515626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537598188	chr9:136515630-136515631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143162172	chr9:136515632-136515633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542698708	chr9:136515647-136515648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549212765	chr9:136515651-136515652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192981766	chr9:136515657-136515658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185217107	chr9:136515662-136515663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61689820	chr9:136515664-136515665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs386416409	chr9:136515674-136515675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572400469	chr9:136515685-136515686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs386416410	chr9:136515687-136515688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs5901024	chr9:136515688-136515689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs199680241	chr9:136515689-136515690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200843888	chr9:136515690-136515691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539630220	chr9:136515691-136515692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558027339	chr9:136515747-136515748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576205164	chr9:136515770-136515771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113505923	chr9:136515816-136515817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543461785	chr9:136515830-136515831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143996855	chr9:136515831-136515832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146431769	chr9:136515836-136515837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189427904	chr9:136515858-136515859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559602506	chr9:136515859-136515860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530784993	chr9:136515894-136515895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545193467	chr9:136515933-136515934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Melanoma	18172304	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Kleefstra Syndrome	21538692	CNVD
Disorders of sex development	22290220	CNVD
Cancer	21183584	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Abnormal phenotypes	18644119	CNVD
Ovarian cancer	21720365	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Hepatocellular carcinoma	22174799	CNVD
Bladder cancer	21909424	CNVD
Cancer	17160897	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20932292	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:393 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136513400-136516200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:136514400-136515400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:136515000-136523400	Weak transcription	Spleen	Spleen
4	chr9:136516200-136516400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr9:136516200-136517000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr9:136517000-136517200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:136517200-136520000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:136518400-136519000	Bivalent Enhancer	HepG2	liver
9	chr9:136518600-136518800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
10	chr9:136518600-136518800	Enhancers	Liver	Liver
11	chr9:136518600-136518800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
12	chr9:136518800-136519000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr9:136519600-136520200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr9:136519600-136521200	Enhancers	Primary T cells from cord blood	blood
15	chr9:136520000-136521600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:136520000-136522000	Bivalent Enhancer	Fetal Thymus	thymus
17	chr9:136520200-136520400	Enhancers	H9 Cell Line	embryonic stem cell
18	chr9:136520200-136520400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
19	chr9:136520200-136520400	Bivalent Enhancer	HMEC	breast
20	chr9:136520200-136520600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr9:136520200-136520600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr9:136520200-136521000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr9:136520200-136521800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr9:136520200-136521800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr9:136520200-136522400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:136520200-136522800	Enhancers	Brain Germinal Matrix	brain
27	chr9:136520200-136524200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr9:136520400-136520600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
29	chr9:136520400-136520600	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr9:136520400-136520600	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr9:136520400-136521200	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr9:136520400-136523600	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr9:136520400-136525800	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr9:136520600-136520800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr9:136520600-136521000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr9:136520600-136521000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
37	chr9:136520600-136521000	Weak transcription	Liver	Liver
38	chr9:136520600-136521000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr9:136520600-136521000	Bivalent Enhancer	Fetal Brain Female	brain
40	chr9:136520600-136521200	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr9:136520600-136521400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr9:136520600-136521800	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr9:136520600-136523000	Weak transcription	Right Atrium	heart
44	chr9:136520800-136521000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr9:136520800-136523400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr9:136521000-136521200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr9:136521000-136521200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr9:136521000-136521200	Bivalent Enhancer	Thymus	Thymus
49	chr9:136521000-136526600	Enhancers	Liver	Liver
50	chr9:136521200-136522200	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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