Variant report

Variant	nsv469906
Chromosome Location	chr9:136494566-136509083
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr9:136500660-136500810	SK-N-SH_RA	brain:	n/a	n/a
2	CTCF	chr9:136502620-136502770	SK-N-SH_RA	brain:	n/a	n/a
3	CTCF	chr9:136498020-136498170	SK-N-SH_RA	brain:	n/a	n/a
4	CTCF	chr9:136498000-136498150	SK-N-SH_RA	brain:	n/a	n/a
5	CTCF	chr9:136504860-136505010	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr9:136501440-136501590	SK-N-SH_RA	brain:	n/a	n/a
7	EP300	chr9:136496722-136504328	SK-N-SH	brain:	n/a	chr9:136503169-136503185 chr9:136499746-136499762 chr9:136501313-136501320 chr9:136497018-136497034 chr9:136499140-136499150
8	EP300	chr9:136500914-136501631	SK-N-SH_RA	brain:	n/a	chr9:136501313-136501320
9	EP300	chr9:136498075-136498359	SK-N-SH_RA	brain:	n/a	n/a
10	EP300	chr9:136498397-136498620	SK-N-SH_RA	brain:	n/a	n/a
11	EP300	chr9:136501003-136501593	SK-N-SH_RA	brain:	n/a	chr9:136501313-136501320
12	EP300	chr9:136498038-136498356	SK-N-SH_RA	brain:	n/a	n/a
13	EP300	chr9:136500223-136500521	SK-N-SH_RA	brain:	n/a	n/a
14	GABPA	chr9:136502721-136503336	H1-hESC	embryonic stem cell:	n/a	n/a
15	GATA2	chr9:136497880-136498383	SH-SY5Y	brain:	n/a	chr9:136498198-136498207
16	GATA2	chr9:136498862-136499440	SH-SY5Y	brain:	n/a	n/a
17	GATA2	chr9:136500996-136501527	SH-SY5Y	brain:	n/a	chr9:136501174-136501181
18	JUND	chr9:136502942-136503115	H1-hESC	embryonic stem cell:	n/a	n/a
19	JUND	chr9:136497727-136497826	HepG2	liver:	n/a	chr9:136497774-136497785
20	MAFK	chr9:136496650-136496713	HepG2	liver:	n/a	n/a
21	MAFK	chr9:136499059-136499168	K562	blood:	n/a	n/a
22	MAX	chr9:136502963-136503365	H1-hESC	embryonic stem cell:	n/a	chr9:136503189-136503199
23	MXI1	chr9:136500841-136504397	SK-N-SH	brain:	n/a	chr9:136501462-136501471 chr9:136502239-136502248
24	MXI1	chr9:136496535-136499781	SK-N-SH	brain:	n/a	n/a
25	MYC	chr9:136502164-136502261	MCF-7	breast:	n/a	chr9:136502250-136502259
26	PBX3	chr9:136501097-136501570	SK-N-SH	brain:	n/a	n/a
27	POLR2A	chr9:136501045-136501726	SK-N-SH	brain:	n/a	n/a
28	POLR2A	chr9:136501076-136501640	SK-N-SH	brain:	n/a	n/a
29	POLR2A	chr9:136498027-136498427	H1-neurons	neurons:	n/a	n/a
30	RAD21	chr9:136500975-136501443	SK-N-SH_RA	brain:	n/a	n/a
31	REST	chr9:136507470-136507779	H1-hESC	embryonic stem cell:	n/a	chr9:136507662-136507671 chr9:136507662-136507682 chr9:136507717-136507730
32	REST	chr9:136507545-136507815	H1-hESC	embryonic stem cell:	n/a	chr9:136507662-136507671 chr9:136507662-136507682 chr9:136507717-136507730
33	REST	chr9:136507394-136507890	ECC-1	luminal epithelium:	n/a	chr9:136507847-136507867 chr9:136507662-136507671 chr9:136507662-136507682 chr9:136507717-136507730
34	REST	chr9:136500982-136501824	SK-N-SH	brain:	n/a	chr9:136501240-136501249 chr9:136501083-136501103 chr9:136501442-136501456 chr9:136501085-136501095
35	REST	chr9:136507590-136507753	Hela-S3	cervix:	n/a	chr9:136507662-136507671 chr9:136507662-136507682 chr9:136507717-136507730
36	REST	chr9:136507606-136507718	HepG2	liver:	n/a	chr9:136507662-136507671 chr9:136507662-136507682
37	REST	chr9:136507530-136507743	PANC-1	pancreas:	n/a	chr9:136507662-136507671 chr9:136507662-136507682 chr9:136507717-136507730
38	REST	chr9:136497848-136498388	SK-N-SH	brain:	n/a	n/a
39	REST	chr9:136507581-136507726	HepG2	liver:	n/a	chr9:136507662-136507671 chr9:136507662-136507682
40	REST	chr9:136507483-136507890	ECC-1	luminal epithelium:	n/a	chr9:136507847-136507867 chr9:136507662-136507671 chr9:136507662-136507682 chr9:136507717-136507730
41	TCF12	chr9:136500932-136501704	SK-N-SH	brain:	n/a	chr9:136501337-136501347
42	TEAD4	chr9:136501081-136501536	SK-N-SH	brain:	n/a	n/a
43	UBTF	chr9:136507293-136507390	K562	blood:	n/a	n/a
44	UBTF	chr9:136503169-136503193	K562	blood:	n/a	n/a
45	UBTF	chr9:136502964-136503034	K562	blood:	n/a	n/a
46	UBTF	chr9:136507357-136507569	K562	blood:	n/a	n/a
47	UBTF	chr9:136499321-136499554	K562	blood:	n/a	n/a
48	USF1	chr9:136500992-136501304	SK-N-SH_RA	brain:	n/a	n/a
49	YY1	chr9:136501090-136501684	SK-N-SH_RA	brain:	n/a	n/a
50	YY1	chr9:136501057-136501865	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:136501772-136501822	NH-A	brain:	n/a
2	chr9:136499189-136499239	MCF-7	breast:	n/a
3	chr9:136499189-136499239	NT2-D1	testis:	n/a
4	chr9:136500234-136500284	SK-N-SH_RA	brain:	n/a
5	chr9:136499189-136499239	GM19239	blood:	n/a
6	chr9:136499189-136499239	HEEpiC	esophagus:	n/a
7	chr9:136500234-136500284	Hela-S3	cervix:	n/a
8	chr9:136499189-136499239	Hela-S3	cervix:	n/a
9	chr9:136501772-136501822	AG04449	skin:	fetal
10	chr9:136499189-136499239	T-47D	breast:	n/a
11	chr9:136501772-136501822	GM12878	blood:	n/a
12	chr9:136500234-136500284	PFSK-1	brain:	n/a
13	chr9:136500234-136500284	AG04450	lung:	fetal
14	chr9:136503185-136503235	NHDF-neo	bronchial:	n/a
15	chr9:136499189-136499239	SKMC	muscle:	n/a
16	chr9:136500855-136500905	HRE	kidney:	n/a
17	chr9:136501784-136501834	PANC-1	pancreas:	n/a
18	chr9:136500234-136500284	CMK	blood:	n/a
19	chr9:136503185-136503235	HIPEpiC	eye:	n/a
20	chr9:136499189-136499239	IMR90	lung:	fetal
21	chr9:136500855-136500905	AG09319	gingival:	n/a
22	chr9:136500234-136500284	HCT-116	colon:	n/a
23	chr9:136499189-136499239	HEK293	kidney:	embryo
24	chr9:136500855-136500905	AoSMC	blood vessel:	n/a
25	chr9:136501772-136501822	BJ	skin:	n/a
26	chr9:136501420-136501470	HIPEpiC	eye:	n/a
27	chr9:136500855-136500905	ovcar-3	ovarian:	n/a
28	chr9:136501784-136501834	BJ	skin:	n/a
29	chr9:136499189-136499239	K562	blood:	n/a
30	chr9:136501420-136501470	Hela-S3	cervix:	n/a
31	chr9:136500855-136500905	PrEC	prostate:	n/a
32	chr9:136500234-136500284	AG09319	gingival:	n/a
33	chr9:136500234-136500284	NT2-D1	testis:	n/a
34	chr9:136499189-136499239	ProgFib	skin:	n/a
35	chr9:136501772-136501822	HAEpiC	amniotic membrane:	n/a
36	chr9:136501772-136501822	Hepatocyte	liver:	n/a
37	chr9:136501420-136501470	HNPCEpiC	eye:	n/a
38	chr9:136500234-136500284	GM19239	blood:	n/a
39	chr9:136501420-136501470	PANC-1	pancreas:	n/a
40	chr9:136500855-136500905	HEEpiC	esophagus:	n/a
41	chr9:136500234-136500284	HUVEC	blood vessel:	n/a
42	chr9:136501772-136501822	NT2-D1	testis:	n/a
43	chr9:136501772-136501822	ovcar-3	ovarian:	n/a
44	chr9:136501772-136501822	HRPEpiC	eye:	n/a
45	chr9:136503185-136503235	HEK293	kidney:	embryo
46	chr9:136501420-136501470	Jurkat	blood:	n/a
47	chr9:136501420-136501470	NH-A	brain:	n/a
48	chr9:136503185-136503235	Caco-2	colon:	n/a
49	chr9:136499189-136499239	HIPEpiC	eye:	n/a
50	chr9:136499189-136499239	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:136500848..136502768-chr9:136506523..136508803,2	K562	blood:
2	chr9:136475965..136477693-chr9:136502084..136503686,2	MCF-7	breast:
3	chr9:136494850..136497208-chr9:136497940..136500332,2	MCF-7	breast:
4	chr9:136499615..136503712-chr9:136504144..136508485,4	K562	blood:
5	chr9:136492846..136495441-chr9:136522709..136525633,2	MCF-7	breast:
6	chr9:136508750..136511596-chr9:136514989..136519879,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM163B-1	chr9:136498109-136498221	ENSG00000261018.1

Variant related genes	Relation type
DBH	TF binding region
ENSG00000261018	TF binding region
DBH	CpG island
ENSG00000261018	CpG island
ENSG00000123454	chromatin interactions
ENSG00000261018	chromatin interactions

Extended variants
information (count: 798 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2519148	chr9:136494566-136494567	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141792905	chr9:136494593-136494594	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs3025369	chr9:136494594-136494595	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs3025370	chr9:136494623-136494624	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs35917724	chr9:136494644-136494645	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12337651	chr9:136494650-136494651	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs536409363	chr9:136494657-136494658	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554882145	chr9:136494691-136494692	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573258483	chr9:136494703-136494704	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534058035	chr9:136494718-136494719	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188060986	chr9:136494721-136494722	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577206223	chr9:136494765-136494766	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545317397	chr9:136494768-136494769	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147748366	chr9:136494779-136494780	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575618668	chr9:136494786-136494787	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377087145	chr9:136494801-136494802	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542808781	chr9:136494812-136494813	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552954638	chr9:136494817-136494818	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190980405	chr9:136494819-136494820	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560954307	chr9:136494825-136494826	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369648138	chr9:136494834-136494835	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539167294	chr9:136494886-136494887	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs372351815	chr9:136494889-136494890	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs546419893	chr9:136494895-136494896	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs564895095	chr9:136494994-136494995	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs531936692	chr9:136495008-136495009	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs550172219	chr9:136495014-136495015	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141080819	chr9:136495028-136495029	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs536572906	chr9:136495031-136495032	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs548739643	chr9:136495034-136495035	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs566985376	chr9:136495067-136495068	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs150199617	chr9:136495132-136495133	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs565777190	chr9:136495167-136495168	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs577417389	chr9:136495223-136495224	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs538201256	chr9:136495227-136495228	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs113249250	chr9:136495229-136495230	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs71505214	chr9:136495230-136495231	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs79503762	chr9:136495239-136495240	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs3025371	chr9:136495248-136495249	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542591281	chr9:136495266-136495267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs561129396	chr9:136495293-136495294	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs138736632	chr9:136495314-136495315	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2519147	chr9:136495318-136495319	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs544366269	chr9:136495360-136495361	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs564789049	chr9:136495373-136495374	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs532096415	chr9:136495394-136495395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs182408818	chr9:136495404-136495405	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs554357961	chr9:136495417-136495418	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs562170430	chr9:136495450-136495451	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs530310387	chr9:136495471-136495472	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Schizophrenia	21346763	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:135 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136493600-136494600	Enhancers	Fetal Brain Male	brain
2	chr9:136494000-136494600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:136494200-136494600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
4	chr9:136494400-136494600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:136494400-136496600	Weak transcription	Fetal Brain Female	brain
6	chr9:136494600-136495200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:136494600-136498400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr9:136494600-136498800	Weak transcription	Fetal Brain Male	brain
9	chr9:136495200-136496400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr9:136496200-136496600	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr9:136496400-136500800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr9:136496600-136496800	Enhancers	Fetal Brain Female	brain
13	chr9:136496800-136497000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr9:136496800-136498800	Weak transcription	Fetal Brain Female	brain
15	chr9:136496800-136501200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
16	chr9:136497000-136498000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr9:136497200-136499800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:136497200-136501200	Enhancers	Fetal Thymus	thymus
19	chr9:136497400-136500800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr9:136497400-136501200	Bivalent Enhancer	Placenta	Placenta
21	chr9:136497800-136499000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:136497800-136500000	Enhancers	H9 Cell Line	embryonic stem cell
23	chr9:136497800-136500000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr9:136497800-136500600	Enhancers	Fetal Lung	lung
25	chr9:136497800-136500800	Enhancers	Brain Germinal Matrix	brain
26	chr9:136497800-136500800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
27	chr9:136498000-136499200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr9:136498000-136499600	Enhancers	Thymus	Thymus
29	chr9:136498000-136499800	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr9:136498000-136500000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr9:136498000-136500000	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr9:136498000-136500200	Enhancers	H1 Cell Line	embryonic stem cell
33	chr9:136498000-136500800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr9:136498000-136501000	Bivalent Enhancer	Fetal Muscle Leg	muscle
35	chr9:136498000-136501800	Bivalent Enhancer	Fetal Stomach	stomach
36	chr9:136498000-136501800	Enhancers	Spleen	Spleen
37	chr9:136498400-136499600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr9:136498400-136501400	Weak transcription	Right Atrium	heart
39	chr9:136498600-136499200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr9:136498800-136499200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr9:136498800-136499400	Enhancers	Fetal Brain Female	brain
42	chr9:136498800-136499600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr9:136498800-136499800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr9:136498800-136500000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr9:136498800-136500200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr9:136498800-136500400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr9:136498800-136500400	Enhancers	Liver	Liver
48	chr9:136498800-136500800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
49	chr9:136498800-136501800	Enhancers	Fetal Brain Male	brain
50	chr9:136499000-136499800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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