Variant report

Variant	nsv612982
Chromosome Location	chr9:95343-129899
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:188)
CpG islands
(count:855)
Chromatin interactive
region (count:0)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:188 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:113631-113796	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr9:114203-114262	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr9:122820-123095	GM12878	blood:	n/a	n/a
4	BATF	chr9:120835-121041	GM12878	blood:	n/a	n/a
5	BATF	chr9:116510-116717	GM12878	blood:	n/a	n/a
6	BCL11A	chr9:117598-117759	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:124340-124557	HepG2	liver:	n/a	n/a
8	CBX3	chr9:94943-95395	K562	blood:	n/a	n/a
9	CHD1	chr9:114025-114199	GM12878	blood:	n/a	n/a
10	CHD2	chr9:99965-100100	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr9:126864-126884	K562	blood:	n/a	n/a
12	CHD2	chr9:114017-114204	GM12878	blood:	n/a	n/a
13	CTBP2	chr9:113094-114323	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr9:113860-114010	GM12865	blood:	n/a	n/a
15	CTCF	chr9:109857-109897	A549	lung:	n/a	n/a
16	CTCF	chr9:114240-114390	GM12866	blood:	n/a	n/a
17	CTCF	chr9:110507-110552	Medullo	brain:	n/a	n/a
18	CTCF	chr9:117460-117610	HEK293	kidney:	n/a	n/a
19	E2F6	chr9:113675-113908	K562	blood:	n/a	chr9:113808-113819
20	E2F6	chr9:113608-114309	K562	blood:	n/a	chr9:113911-113921 chr9:113993-114005 chr9:114296-114307 chr9:113997-114004 chr9:114260-114269 chr9:113808-113819 chr9:113997-114004 chr9:113997-114004
21	E2F6	chr9:114137-114314	K562	blood:	n/a	chr9:114296-114307 chr9:114260-114269
22	E2F6	chr9:113609-114107	K562	blood:	n/a	chr9:113911-113921 chr9:113993-114005 chr9:113997-114004 chr9:113808-113819 chr9:113997-114004 chr9:113997-114004
23	EBF1	chr9:116769-117403	GM12878	blood:	n/a	n/a
24	EBF1	chr9:117522-117937	GM12878	blood:	n/a	n/a
25	EGR1	chr9:113573-113921	K562	blood:	n/a	n/a
26	EGR1	chr9:113559-113853	K562	blood:	n/a	n/a
27	ELF1	chr9:113955-114347	GM12878	blood:	n/a	n/a
28	ELF1	chr9:113350-113851	GM12878	blood:	n/a	chr9:113564-113576 chr9:113821-113833 chr9:113625-113634
29	EP300	chr9:122794-123086	GM12878	blood:	n/a	n/a
30	EP300	chr9:110065-110292	GM12878	blood:	n/a	n/a
31	EP300	chr9:121886-122120	GM12878	blood:	n/a	n/a
32	FOS	chr9:109685-109872	MCF10A-Er-Src	breast:	n/a	chr9:109751-109760 chr9:109750-109759
33	FOS	chr9:109672-109872	MCF10A-Er-Src	breast:	n/a	chr9:109751-109760 chr9:109750-109759
34	FOSL2	chr9:120248-120494	HepG2	liver:	n/a	chr9:120255-120269
35	FOSL2	chr9:116314-119003	HepG2	liver:	n/a	n/a
36	FOSL2	chr9:115068-115454	HepG2	liver:	n/a	n/a
37	FOSL2	chr9:119045-119485	HepG2	liver:	n/a	n/a
38	FOSL2	chr9:109517-109933	HepG2	liver:	n/a	chr9:109751-109760 chr9:109750-109759 chr9:109563-109572
39	FOXA2	chr9:119327-119826	A549	lung:	n/a	n/a
40	GABPA	chr9:119384-119568	Hela-S3	cervix:	n/a	n/a
41	GABPA	chr9:119448-119562	Hela-S3	cervix:	n/a	n/a
42	GATA1	chr9:116828-117049	PBDE	blood:	n/a	n/a
43	GATA2	chr9:123655-123946	K562	blood:	n/a	n/a
44	GATA2	chr9:94813-95631	K562	blood:	n/a	n/a
45	HEY1	chr9:126023-126285	HepG2	liver:	n/a	n/a
46	HEY1	chr9:119097-119455	HepG2	liver:	n/a	n/a
47	HEY1	chr9:94973-95530	K562	blood:	n/a	n/a
48	HEY1	chr9:114047-114253	K562	blood:	n/a	n/a
49	HEY1	chr9:95006-95589	K562	blood:	n/a	n/a
50	IRF4	chr9:96498-96852	GM12878	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	chr9:114140-114190	HAEpiC	amniotic membrane:	n/a
2	chr9:114140-114190	HAEpiC	amniotic membrane:	n/a
3	chr9:114359-114409	SK-N-SH	brain:	n/a
4	chr9:112618-112668	HRPEpiC	eye:	n/a
5	chr9:113530-113580	HUVEC	blood vessel:	n/a
6	chr9:112618-112668	HAEpiC	amniotic membrane:	n/a
7	chr9:112937-112987	HRE	kidney:	n/a
8	chr9:112937-112987	H1-hESC	embryonic stem cell:	embryo
9	chr9:104568-104618	HCM	heart:	n/a
10	chr9:114838-114888	MCF-7	breast:	n/a
11	chr9:112937-112987	NB4	blood:	n/a
12	chr9:114359-114409	HMEC	breast:	n/a
13	chr9:117608-117658	AG10803	skin:	n/a
14	chr9:114434-114484	H1-hESC	embryonic stem cell:	embryo
15	chr9:114359-114409	HCT-116	colon:	n/a
16	chr9:114838-114888	HRPEpiC	eye:	n/a
17	chr9:112618-112668	ProgFib	skin:	n/a
18	chr9:112937-112987	PrEC	prostate:	n/a
19	chr9:118091-118141	AG04449	skin:	fetal
20	chr9:104568-104618	HAEpiC	amniotic membrane:	n/a
21	chr9:117044-117094	IMR90	lung:	fetal
22	chr9:117044-117094	HPAEpiC	pulmonary alveolar:	n/a
23	chr9:117608-117658	HEEpiC	esophagus:	n/a
24	chr9:117608-117658	HRPEpiC	eye:	n/a
25	chr9:112618-112668	SK-N-MC	brain:	n/a
26	chr9:114838-114888	HIPEpiC	eye:	n/a
27	chr9:109039-109089	ProgFib	skin:	n/a
28	chr9:114359-114409	AoSMC	blood vessel:	n/a
29	chr9:104568-104618	HCPEpiC	choroid plexus:	n/a
30	chr9:118698-118748	HUVEC	blood vessel:	n/a
31	chr9:113530-113580	HEEpiC	esophagus:	n/a
32	chr9:113530-113580	NH-A	brain:	n/a
33	chr9:114140-114190	HepG2	liver:	n/a
34	chr9:114140-114190	NHBE	bronchial:	n/a
35	chr9:117044-117094	HCT-116	colon:	n/a
36	chr9:117608-117658	GM12891	blood:	n/a
37	chr9:118530-118580	GM19239	blood:	n/a
38	chr9:112618-112668	K562	blood:	n/a
39	chr9:104568-104618	NB4	blood:	n/a
40	chr9:104568-104618	HMEC	breast:	n/a
41	chr9:112618-112668	PANC-1	pancreas:	n/a
42	chr9:109039-109089	LNCaP	prostate:	n/a
43	chr9:109039-109089	SK-N-MC	brain:	n/a
44	chr9:114838-114888	Hela-S3	cervix:	n/a
45	chr9:109039-109089	PrEC	prostate:	n/a
46	chr9:109039-109089	ovcar-3	ovarian:	n/a
47	chr9:109039-109089	HCPEpiC	choroid plexus:	n/a
48	chr9:114838-114888	T-47D	breast:	n/a
49	chr9:112618-112668	Jurkat	blood:	n/a
50	chr9:112618-112668	HNPCEpiC	eye:	n/a

No data

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXD4-3	chr9:114040-115772	NONHSAT129899
2	lnc-FOXD4-2	chr9:109596-109842	NONHSAT129897
3	lnc-FOXD4-2	chr9:109316-109471	NONHSAT129895
4	lnc-FOXD4-3	chr9:113606-113656	NONHSAT129899
5	lnc-FOXD4-2	chr9:101002-101304	ENSG00000227917
6	lnc-FOXD4-1	chr9:112716-113067	ENSG00000231808
7	lnc-FOXD4-1	chr9:113694-113754	ENSG00000231808
8	lnc-FOXD4-2	chr9:102740-102850	NONHSAT129895
9	lnc-FOXD4-2	chr9:101014-101304	NONHSAT129895
10	lnc-FOXD4-2	chr9:102740-102941	ENSG00000227917
11	lnc-FOXD4-2	chr9:108804-109469	NONHSAT129897
12	lnc-FOXD4-2	chr9:102716-103067	NONHSAT129896
13	lnc-FOXD4-2	chr9:102473-102541	ENSG00000227917
14	lnc-FOXD4-2	chr9:103694-103754	NONHSAT129896

No data

Variant related genes	Relation type
ENSG00000231808	TF binding region
FOXD4	TF binding region
ENSG00000227917	TF binding region
CBWD1	TF binding region
ENSG00000231808	CpG island
FOXD4	CpG island
ENSG00000227917	CpG island
CBWD1	CpG island

Extended variants
information (count: 970 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:970 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9408743	chr9:95343-95344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2811118	chr9:95353-95354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115805219	chr9:95385-95386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112834062	chr9:95438-95439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544987307	chr9:95520-95521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149438654	chr9:95533-95534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527558774	chr9:95546-95547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548798434	chr9:95553-95554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141575069	chr9:95574-95575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531354983	chr9:95582-95583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200086301	chr9:95584-95585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549803904	chr9:95593-95594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571166833	chr9:95613-95614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538594666	chr9:95627-95628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552125631	chr9:95662-95663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567200479	chr9:95673-95674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534481775	chr9:95675-95676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556042917	chr9:95687-95688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574237997	chr9:95708-95709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537962861	chr9:95757-95758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs201016932	chr9:95780-95781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146185791	chr9:95787-95788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577974863	chr9:95799-95800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181414710	chr9:98001-98002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559462679	chr9:98036-98037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529790705	chr9:98075-98076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541878739	chr9:98097-98098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563126855	chr9:98098-98099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532076671	chr9:98115-98116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186490349	chr9:98116-98117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550163316	chr9:98126-98127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150977810	chr9:98139-98140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532536874	chr9:98145-98146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547509116	chr9:98175-98176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs62532139	chr9:98194-98195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565864844	chr9:98255-98256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs200544582	chr9:98303-98304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140408941	chr9:98326-98327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569949270	chr9:98335-98336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537359468	chr9:98339-98340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558537182	chr9:98443-98444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529362353	chr9:98475-98476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188582569	chr9:98492-98493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181062233	chr9:98555-98556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs78327442	chr9:98560-98561	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
46	rs566227594	chr9:98590-98591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545148929	chr9:98657-98658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574623804	chr9:98728-98729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2257954	chr9:101026-101027	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs568968775	chr9:101033-101034	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD
Intracranial ependymoma	16609018	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94000-95600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr9:95000-95800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr9:95200-95600	Enhancers	K562	blood
4	chr9:98000-98400	Enhancers	Primary T cells fromperipheralblood	blood
5	chr9:98000-98600	Enhancers	Primary B cells from peripheral blood	blood
6	chr9:98000-98600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr9:98000-98800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
8	chr9:102600-102800	ZNF genes & repeats	Lung	lung
9	chr9:108800-109000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
10	chr9:108800-109000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
11	chr9:108800-109000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
12	chr9:108800-109000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr9:109200-109400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
14	chr9:109200-109400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:109200-109400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr9:109200-110000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
17	chr9:112800-113000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
18	chr9:112800-113000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
19	chr9:112800-113000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
20	chr9:112800-113000	Bivalent Enhancer	Brain Hippocampus Middle	brain
21	chr9:112800-113000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
22	chr9:112800-113000	Bivalent Enhancer	K562	blood
23	chr9:112800-113200	Bivalent Enhancer	Fetal Muscle Leg	muscle
24	chr9:112800-113400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
25	chr9:112800-113400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
26	chr9:112800-113400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
27	chr9:112800-113400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
28	chr9:112800-113400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr9:112800-113400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr9:112800-113400	Bivalent Enhancer	Adipose Nuclei	Adipose
31	chr9:112800-113400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
32	chr9:112800-113400	Bivalent/Poised TSS	Right Ventricle	heart
33	chr9:112800-113400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
34	chr9:112800-113600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
35	chr9:112800-113600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr9:112800-113800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
37	chr9:112800-113800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
38	chr9:112800-114000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
39	chr9:112800-115200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
40	chr9:112800-115400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
41	chr9:113000-113200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:113000-113200	Active TSS	Primary hematopoietic stem cells short term culture	blood
43	chr9:113000-113200	Bivalent Enhancer	Fetal Intestine Large	intestine
44	chr9:113000-113400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
45	chr9:113000-113400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
46	chr9:113000-113400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr9:113000-113400	Bivalent Enhancer	Brain Germinal Matrix	brain
48	chr9:113000-113800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
49	chr9:113000-113800	Bivalent Enhancer	Placenta	Placenta
50	chr9:113000-114400	Active TSS	K562	blood

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