Variant report

Variant	nsv972637
Chromosome Location	chr9:93226-121450
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	ARID3A	chr9:95057-95158	K562	blood:	n/a	n/a
2	ARID3A	chr9:94438-94633	K562	blood:	n/a	chr9:94582-94598
3	ATF1	chr9:94435-94576	K562	blood:	n/a	n/a
4	BACH1	chr9:113631-113796	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:114203-114262	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr9:116510-116717	GM12878	blood:	n/a	n/a
7	BATF	chr9:120835-121041	GM12878	blood:	n/a	n/a
8	BCL11A	chr9:117598-117759	GM12878	blood:	n/a	n/a
9	CBX3	chr9:94943-95395	K562	blood:	n/a	n/a
10	CEBPB	chr9:94900-95314	K562	blood:	n/a	n/a
11	CEBPD	chr9:94950-95338	K562	blood:	n/a	n/a
12	CHD1	chr9:114025-114199	GM12878	blood:	n/a	n/a
13	CHD2	chr9:114017-114204	GM12878	blood:	n/a	n/a
14	CHD2	chr9:99965-100100	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr9:113094-114323	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr9:110507-110552	Medullo	brain:	n/a	n/a
17	CTCF	chr9:113860-114010	GM12865	blood:	n/a	n/a
18	CTCF	chr9:117460-117610	HEK293	kidney:	n/a	n/a
19	CTCF	chr9:109857-109897	A549	lung:	n/a	n/a
20	CTCF	chr9:114240-114390	GM12866	blood:	n/a	n/a
21	E2F4	chr9:94444-94576	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F6	chr9:113675-113908	K562	blood:	n/a	chr9:113808-113819
23	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
24	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
25	E2F6	chr9:114137-114314	K562	blood:	n/a	chr9:114296-114307 chr9:114260-114269
26	EBF1	chr9:117522-117937	GM12878	blood:	n/a	n/a
27	EBF1	chr9:116769-117403	GM12878	blood:	n/a	n/a
28	EGR1	chr9:113573-113921	K562	blood:	n/a	n/a
29	EGR1	chr9:113559-113853	K562	blood:	n/a	n/a
30	ELF1	chr9:113350-113851	GM12878	blood:	n/a	chr9:113564-113576 chr9:113821-113833 chr9:113625-113634
31	ELF1	chr9:113955-114347	GM12878	blood:	n/a	n/a
32	EP300	chr9:110065-110292	GM12878	blood:	n/a	n/a
33	EP300	chr9:94959-95297	K562	blood:	n/a	chr9:95130-95144
34	EP300	chr9:94395-94590	K562	blood:	n/a	chr9:94493-94502
35	FOS	chr9:94374-94636	MCF10A-Er-Src	breast:	n/a	chr9:94495-94502 chr9:94493-94502
36	FOS	chr9:94399-94636	MCF10A-Er-Src	breast:	n/a	chr9:94495-94502 chr9:94493-94502
37	FOS	chr9:94425-94625	HUVEC	blood vessel:	n/a	chr9:94495-94502 chr9:94493-94502
38	FOS	chr9:109685-109872	MCF10A-Er-Src	breast:	n/a	chr9:109751-109760 chr9:109750-109759
39	FOS	chr9:109672-109872	MCF10A-Er-Src	breast:	n/a	chr9:109751-109760 chr9:109750-109759
40	FOS	chr9:94374-94600	MCF10A-Er-Src	breast:	n/a	chr9:94495-94502 chr9:94493-94502
41	FOS	chr9:94375-94636	MCF10A-Er-Src	breast:	n/a	chr9:94495-94502 chr9:94493-94502
42	FOSL2	chr9:116314-119003	HepG2	liver:	n/a	n/a
43	FOSL2	chr9:115068-115454	HepG2	liver:	n/a	n/a
44	FOSL2	chr9:109517-109933	HepG2	liver:	n/a	chr9:109751-109760 chr9:109750-109759 chr9:109563-109572
45	FOSL2	chr9:120248-120494	HepG2	liver:	n/a	chr9:120255-120269
46	FOSL2	chr9:119045-119485	HepG2	liver:	n/a	n/a
47	FOXA2	chr9:119327-119826	A549	lung:	n/a	n/a
48	GABPA	chr9:119384-119568	Hela-S3	cervix:	n/a	n/a
49	GABPA	chr9:119448-119562	Hela-S3	cervix:	n/a	n/a
50	GATA1	chr9:116828-117049	PBDE	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:118698-118748	AG09309	skin:	n/a
2	chr9:112937-112987	SAEC	small airway:	n/a
3	chr9:118530-118580	HNPCEpiC	eye:	n/a
4	chr9:114359-114409	GM06990	blood:	n/a
5	chr9:113530-113580	MCF10A-Er-Src	breast:	n/a
6	chr9:118698-118748	AG09309	skin:	n/a
7	chr9:112937-112987	SAEC	small airway:	n/a
8	chr9:118530-118580	HNPCEpiC	eye:	n/a
9	chr9:114359-114409	GM06990	blood:	n/a
10	chr9:113530-113580	MCF10A-Er-Src	breast:	n/a
11	chr9:118530-118580	T-47D	breast:	n/a
12	chr9:109039-109089	Hepatocyte	liver:	n/a
13	chr9:113530-113580	SKMC	muscle:	n/a
14	chr9:114359-114409	ECC-1	luminal epithelium:	n/a
15	chr9:118530-118580	HUVEC	blood vessel:	n/a
16	chr9:118530-118580	HepG2	liver:	n/a
17	chr9:118698-118748	HepG2	liver:	n/a
18	chr9:118091-118141	HMEC	breast:	n/a
19	chr9:114838-114888	AG04449	skin:	fetal
20	chr9:117608-117658	BJ	skin:	n/a
21	chr9:114434-114484	A549	lung:	n/a
22	chr9:112937-112987	AG10803	skin:	n/a
23	chr9:109039-109089	AG10803	skin:	n/a
24	chr9:117044-117094	AoSMC	blood vessel:	n/a
25	chr9:118091-118141	HL-60	blood:	n/a
26	chr9:114838-114888	Hepatocyte	liver:	n/a
27	chr9:118530-118580	AG10803	skin:	n/a
28	chr9:118091-118141	RPTEC	kidney:	n/a
29	chr9:114359-114409	HEEpiC	esophagus:	n/a
30	chr9:114359-114409	RPTEC	kidney:	n/a
31	chr9:112618-112668	IMR90	lung:	fetal
32	chr9:112937-112987	PrEC	prostate:	n/a
33	chr9:117044-117094	SAEC	small airway:	n/a
34	chr9:117608-117658	HUVEC	blood vessel:	n/a
35	chr9:118530-118580	AG09309	skin:	n/a
36	chr9:114359-114409	PrEC	prostate:	n/a
37	chr9:114359-114409	ProgFib	skin:	n/a
38	chr9:114140-114190	Hela-S3	cervix:	n/a
39	chr9:112937-112987	AG04449	skin:	fetal
40	chr9:118698-118748	SAEC	small airway:	n/a
41	chr9:114140-114190	GM12891	blood:	n/a
42	chr9:112937-112987	ECC-1	luminal epithelium:	n/a
43	chr9:113530-113580	RPTEC	kidney:	n/a
44	chr9:109039-109089	NHDF-neo	bronchial:	n/a
45	chr9:104568-104618	BE2_C	brain:	n/a
46	chr9:118698-118748	HEK293	kidney:	embryo
47	chr9:114140-114190	GM12878	blood:	n/a
48	chr9:104568-104618	HRCEpiC	kidney:	n/a
49	chr9:109039-109089	HUVEC	blood vessel:	n/a
50	chr9:117608-117658	A549	lung:	n/a

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

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

Extended variants
information (count: 752 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:752 , 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	rs530965328	chr9:93259-93260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371473192	chr9:93310-93311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564393524	chr9:93367-93368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528566157	chr9:93372-93373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547052973	chr9:93412-93413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568458411	chr9:93421-93422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145650527	chr9:93432-93433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535638418	chr9:93438-93439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7033040	chr9:93440-93441	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
10	rs569043699	chr9:93465-93466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539224768	chr9:93470-93471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9408741	chr9:93480-93481	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
13	rs371465127	chr9:93558-93559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111567539	chr9:93560-93561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182832343	chr9:93561-93562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554990436	chr9:93563-93564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188202095	chr9:93579-93580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542124791	chr9:93643-93644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563792630	chr9:93720-93721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575814742	chr9:93758-93759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535280032	chr9:93791-93792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546111578	chr9:93825-93826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564688315	chr9:93826-93827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375103347	chr9:93864-93865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547115795	chr9:93941-93942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562067319	chr9:93969-93970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529264597	chr9:94010-94011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2492163	chr9:94018-94019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372138497	chr9:94041-94042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569030113	chr9:94135-94136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539704145	chr9:94146-94147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191399094	chr9:94147-94148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142466132	chr9:94159-94160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs151244373	chr9:94167-94168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555000764	chr9:94172-94173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140470254	chr9:94197-94198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537418316	chr9:94241-94242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556099995	chr9:94266-94267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200727570	chr9:94308-94309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575885482	chr9:94390-94391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546469330	chr9:94392-94393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558118129	chr9:94428-94429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573430051	chr9:94440-94441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540740648	chr9:94473-94474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562130041	chr9:94481-94482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576901717	chr9:94488-94489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544308205	chr9:94530-94531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147682809	chr9:94552-94553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533121122	chr9:94559-94560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551604684	chr9:94575-94576	Enhancers Weak transcription	n/a	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:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:88600-94000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr9:94000-94200	Enhancers	K562	blood
3	chr9:94000-95600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:94200-95200	Weak transcription	K562	blood
5	chr9:95000-95800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr9:95200-95600	Enhancers	K562	blood
7	chr9:98000-98400	Enhancers	Primary T cells fromperipheralblood	blood
8	chr9:98000-98600	Enhancers	Primary B cells from peripheral blood	blood
9	chr9:98000-98600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr9:98000-98800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
11	chr9:102600-102800	ZNF genes & repeats	Lung	lung
12	chr9:108800-109000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
13	chr9:108800-109000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:108800-109000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
15	chr9:108800-109000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr9:109200-109400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
17	chr9:109200-109400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr9:109200-109400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr9:109200-110000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
20	chr9:112800-113000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
21	chr9:112800-113000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
22	chr9:112800-113000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
23	chr9:112800-113000	Bivalent Enhancer	Brain Hippocampus Middle	brain
24	chr9:112800-113000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
25	chr9:112800-113000	Bivalent Enhancer	K562	blood
26	chr9:112800-113200	Bivalent Enhancer	Fetal Muscle Leg	muscle
27	chr9:112800-113400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
28	chr9:112800-113400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
29	chr9:112800-113400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
30	chr9:112800-113400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
31	chr9:112800-113400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr9:112800-113400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr9:112800-113400	Bivalent Enhancer	Adipose Nuclei	Adipose
34	chr9:112800-113400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
35	chr9:112800-113400	Bivalent/Poised TSS	Right Ventricle	heart
36	chr9:112800-113400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
37	chr9:112800-113600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
38	chr9:112800-113600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr9:112800-113800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
40	chr9:112800-113800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
41	chr9:112800-114000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
42	chr9:112800-115200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
43	chr9:112800-115400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
44	chr9:113000-113200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr9:113000-113200	Active TSS	Primary hematopoietic stem cells short term culture	blood
46	chr9:113000-113200	Bivalent Enhancer	Fetal Intestine Large	intestine
47	chr9:113000-113400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
48	chr9:113000-113400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
49	chr9:113000-113400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr9:113000-113400	Bivalent Enhancer	Brain Germinal Matrix	brain

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