Variant report

Variant	nsv891941
Chromosome Location	chr9:84832-208549
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1136)
CpG islands
(count:1039)
Chromatin interactive
region (count:3)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1136 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:94438-94633	K562	blood:	n/a	chr9:94582-94598
2	ARID3A	chr9:95057-95158	K562	blood:	n/a	n/a
3	ATF1	chr9:94435-94576	K562	blood:	n/a	n/a
4	BACH1	chr9:207498-207603	K562	blood:	n/a	n/a
5	BACH1	chr9:114203-114262	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:113631-113796	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr9:116510-116717	GM12878	blood:	n/a	n/a
8	BATF	chr9:120835-121041	GM12878	blood:	n/a	n/a
9	BATF	chr9:185826-186168	GM12878	blood:	n/a	n/a
10	BATF	chr9:199669-200113	GM12878	blood:	n/a	n/a
11	BATF	chr9:183636-184093	GM12878	blood:	n/a	n/a
12	BATF	chr9:156921-157465	GM12878	blood:	n/a	n/a
13	BATF	chr9:122820-123095	GM12878	blood:	n/a	n/a
14	BATF	chr9:198812-199262	GM12878	blood:	n/a	chr9:198886-198895
15	BATF	chr9:160145-160379	GM12878	blood:	n/a	n/a
16	BATF	chr9:164778-164998	GM12878	blood:	n/a	n/a
17	BATF	chr9:156635-156839	GM12878	blood:	n/a	n/a
18	BATF	chr9:178082-178323	GM12878	blood:	n/a	n/a
19	BATF	chr9:184216-185020	GM12878	blood:	n/a	chr9:184501-184509
20	BATF	chr9:200387-200708	GM12878	blood:	n/a	chr9:200519-200530
21	BATF	chr9:178036-178376	GM12878	blood:	n/a	n/a
22	BATF	chr9:156608-156841	GM12878	blood:	n/a	n/a
23	BATF	chr9:167629-168111	GM12878	blood:	n/a	n/a
24	BATF	chr9:88665-89067	GM12878	blood:	n/a	chr9:88843-88853 chr9:88842-88853
25	BATF	chr9:178645-179348	GM12878	blood:	n/a	chr9:179069-179082
26	BATF	chr9:88649-88891	GM12878	blood:	n/a	chr9:88843-88853 chr9:88842-88853
27	BATF	chr9:184237-185449	GM12878	blood:	n/a	chr9:184501-184509
28	BATF	chr9:185844-186146	GM12878	blood:	n/a	n/a
29	BATF	chr9:167541-168102	GM12878	blood:	n/a	n/a
30	BATF	chr9:198874-199092	GM12878	blood:	n/a	chr9:198886-198895
31	BATF	chr9:183522-184128	GM12878	blood:	n/a	n/a
32	BATF	chr9:194727-194900	GM12878	blood:	n/a	n/a
33	BATF	chr9:152906-153110	GM12878	blood:	n/a	chr9:152982-152993
34	BATF	chr9:199639-200066	GM12878	blood:	n/a	n/a
35	BATF	chr9:156926-157447	GM12878	blood:	n/a	n/a
36	BATF	chr9:178394-179363	GM12878	blood:	n/a	chr9:179069-179082
37	BATF	chr9:185181-185422	GM12878	blood:	n/a	n/a
38	BATF	chr9:177184-177383	GM12878	blood:	n/a	n/a
39	BCL11A	chr9:164593-164855	GM12878	blood:	n/a	n/a
40	BCL11A	chr9:169277-169515	GM12878	blood:	n/a	n/a
41	BCL11A	chr9:153305-153607	GM12878	blood:	n/a	n/a
42	BCL11A	chr9:178105-179362	GM12878	blood:	n/a	n/a
43	BCL11A	chr9:198891-199091	GM12878	blood:	n/a	n/a
44	BCL11A	chr9:183794-184108	GM12878	blood:	n/a	n/a
45	BCL11A	chr9:160125-160430	GM12878	blood:	n/a	n/a
46	BCL11A	chr9:117598-117759	GM12878	blood:	n/a	n/a
47	BCL11A	chr9:185858-186302	GM12878	blood:	n/a	n/a
48	BCL11A	chr9:184246-185366	GM12878	blood:	n/a	n/a
49	BCL11A	chr9:156917-157457	GM12878	blood:	n/a	n/a
50	BCL11A	chr9:151681-151909	GM12878	blood:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:179409-179459	T-47D	breast:	n/a
2	chr9:113530-113580	ProgFib	skin:	n/a
3	chr9:179409-179459	T-47D	breast:	n/a
4	chr9:113530-113580	ProgFib	skin:	n/a
5	chr9:114434-114484	AG04449	skin:	fetal
6	chr9:114838-114888	Hepatocyte	liver:	n/a
7	chr9:117608-117658	BJ	skin:	n/a
8	chr9:109039-109089	HAEpiC	amniotic membrane:	n/a
9	chr9:112618-112668	HPAEpiC	pulmonary alveolar:	n/a
10	chr9:118091-118141	HPAEpiC	pulmonary alveolar:	n/a
11	chr9:112937-112987	SK-N-MC	brain:	n/a
12	chr9:112618-112668	MCF10A-Er-Src	breast:	n/a
13	chr9:112618-112668	ECC-1	luminal epithelium:	n/a
14	chr9:179409-179459	U87	brain:	n/a
15	chr9:118698-118748	GM19239	blood:	n/a
16	chr9:118698-118748	PFSK-1	brain:	n/a
17	chr9:118530-118580	NT2-D1	testis:	n/a
18	chr9:114434-114484	GM19239	blood:	n/a
19	chr9:118698-118748	Jurkat	blood:	n/a
20	chr9:104568-104618	HMEC	breast:	n/a
21	chr9:114140-114190	PFSK-1	brain:	n/a
22	chr9:118530-118580	K562	blood:	n/a
23	chr9:113530-113580	NHDF-neo	bronchial:	n/a
24	chr9:118530-118580	IMR90	lung:	fetal
25	chr9:114838-114888	SK-N-MC	brain:	n/a
26	chr9:118698-118748	SAEC	small airway:	n/a
27	chr9:117608-117658	NHDF-neo	bronchial:	n/a
28	chr9:114140-114190	SK-N-MC	brain:	n/a
29	chr9:168828-168878	HRCEpiC	kidney:	n/a
30	chr9:176893-176943	HUVEC	blood vessel:	n/a
31	chr9:114434-114484	PFSK-1	brain:	n/a
32	chr9:117044-117094	GM19239	blood:	n/a
33	chr9:117044-117094	K562	blood:	n/a
34	chr9:118698-118748	AG09319	gingival:	n/a
35	chr9:113530-113580	AG09319	gingival:	n/a
36	chr9:113530-113580	AG04449	skin:	fetal
37	chr9:118530-118580	GM19239	blood:	n/a
38	chr9:118091-118141	HEEpiC	esophagus:	n/a
39	chr9:179409-179459	IMR90	lung:	fetal
40	chr9:104568-104618	Hela-S3	cervix:	n/a
41	chr9:114838-114888	HEEpiC	esophagus:	n/a
42	chr9:179409-179459	HIPEpiC	eye:	n/a
43	chr9:114838-114888	GM19239	blood:	n/a
44	chr9:179409-179459	Jurkat	blood:	n/a
45	chr9:112618-112668	AG09309	skin:	n/a
46	chr9:113530-113580	HRE	kidney:	n/a
47	chr9:112937-112987	NHBE	bronchial:	n/a
48	chr9:179409-179459	HRE	kidney:	n/a
49	chr9:176893-176943	HMEC	breast:	n/a
50	chr9:179409-179459	H1-hESC	embryonic stem cell:	embryo

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:207715..211592-chr9:270281..275557,5	K562	blood:
2	chr9:207956..209819-chr9:211466..213662,2	MCF-7	breast:
3	chr9:207871..210695-chr9:212521..216858,5	MCF-7	breast:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXD4-5	chr9:154709-154795	NONHSAT129910
2	lnc-FOXD4-5	chr9:156481-156527	NONHSAT129910
3	lnc-FOXD4-3	chr9:114040-115772	NONHSAT129899
4	lnc-FOXD4-5	chr9:161567-161647	NONHSAT129910
5	lnc-FOXD4-2	chr9:109316-109471	NONHSAT129895
6	lnc-FOXD4-2	chr9:102740-102941	ENSG00000227917
7	lnc-FOXD4-4	chr9:90804-91304	NONHSAT129892
8	lnc-FOXD4-4	chr9:92473-92541	NONHSAT129893
9	lnc-FOXD4-1	chr9:112716-113067	ENSG00000231808
10	lnc-FOXD4-2	chr9:102473-102541	ENSG00000227917
11	lnc-FOXD4-4	chr9:92740-92850	NONHSAT129892
12	lnc-FOXD4-2	chr9:103694-103754	NONHSAT129896
13	lnc-FOXD4-3	chr9:113606-113656	NONHSAT129899
14	lnc-FOXD4-5	chr9:151745-152078	NONHSAT129910
15	lnc-FOXD4-4	chr9:92740-92941	ucscGeneNc_uc003zfy_2
16	lnc-FOXD4-4	chr9:92473-92541	ucscGeneNc_uc003zfy_2
17	lnc-FOXD4-2	chr9:108804-109469	NONHSAT129897
18	lnc-FOXD4-4	chr9:92740-92941	NONHSAT129893
19	lnc-FOXD4-2	chr9:101014-101304	NONHSAT129895
20	lnc-DOCK8-3	chr9:88742-88826	ENSG00000225655.1
21	lnc-FOXD4-2	chr9:109596-109842	NONHSAT129897
22	lnc-FOXD4-4	chr9:90995-91304	ucscGeneNc_uc003zfy_2
23	lnc-FOXD4-2	chr9:102716-103067	NONHSAT129896
24	lnc-FOXD4-2	chr9:102740-102850	NONHSAT129895
25	lnc-FOXD4-1	chr9:113694-113754	ENSG00000231808
26	lnc-FOXD4-2	chr9:101002-101304	ENSG00000227917
27	lnc-FOXD4-4	chr9:91002-91304	NONHSAT129893

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
ENSG00000235880	chromatin interactions
ENSG00000107099	chromatin interactions
ENSG00000183784	chromatin interactions

Extended variants
information (count: 3546 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:3546 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2811095	chr9:86435-86436	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537529489	chr9:86460-86461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555777075	chr9:86469-86470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375939573	chr9:86480-86481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs56191501	chr9:86485-86486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192677420	chr9:86495-86496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527667467	chr9:86521-86522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs28537397	chr9:86545-86546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184510436	chr9:86548-86549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570876565	chr9:86553-86554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540444821	chr9:86568-86569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562246092	chr9:86601-86602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529442142	chr9:86647-86648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200937059	chr9:86656-86657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140698043	chr9:86668-86669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs202222721	chr9:86684-86685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551085043	chr9:86705-86706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562873904	chr9:86716-86717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533133545	chr9:86735-86736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551668007	chr9:86775-86776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs28738812	chr9:86784-86785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534070879	chr9:86792-86793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527627369	chr9:87827-87828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548859900	chr9:87832-87833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549970592	chr9:87841-87842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149151454	chr9:87969-87970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181922103	chr9:87970-87971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs55876001	chr9:88000-88001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148314554	chr9:88011-88012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs56706531	chr9:88022-88023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184825310	chr9:88054-88055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571228833	chr9:88091-88092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs56091827	chr9:88120-88121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs59314848	chr9:88122-88123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2811102	chr9:88130-88131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374474726	chr9:88161-88162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553522858	chr9:88187-88188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141470825	chr9:88205-88206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2811103	chr9:88210-88211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374940288	chr9:88211-88212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534271289	chr9:88215-88216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556055379	chr9:88219-88220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs59820801	chr9:88229-88230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569906079	chr9:88233-88234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370905533	chr9:88237-88238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138845971	chr9:88238-88239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs374537962	chr9:88241-88242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368829200	chr9:88245-88246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2811104	chr9:88254-88255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544786928	chr9:88267-88268	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Myelodysplastic syndrome	21251322	CNVD
Primary immunodeficiency	22942019	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:804 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:86400-86800	Enhancers	Fetal Thymus	thymus
2	chr9:87800-88600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:88400-88600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:88600-94000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr9:94000-94200	Enhancers	K562	blood
6	chr9:94000-95600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:94200-95200	Weak transcription	K562	blood
8	chr9:95000-95800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr9:95200-95600	Enhancers	K562	blood
10	chr9:98000-98400	Enhancers	Primary T cells fromperipheralblood	blood
11	chr9:98000-98600	Enhancers	Primary B cells from peripheral blood	blood
12	chr9:98000-98600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr9:98000-98800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr9:102600-102800	ZNF genes & repeats	Lung	lung
15	chr9:108800-109000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
16	chr9:108800-109000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
17	chr9:108800-109000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
18	chr9:108800-109000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr9:109200-109400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
20	chr9:109200-109400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr9:109200-109400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr9:109200-110000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
23	chr9:112800-113000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
24	chr9:112800-113000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
25	chr9:112800-113000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
26	chr9:112800-113000	Bivalent Enhancer	Brain Hippocampus Middle	brain
27	chr9:112800-113000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
28	chr9:112800-113000	Bivalent Enhancer	K562	blood
29	chr9:112800-113200	Bivalent Enhancer	Fetal Muscle Leg	muscle
30	chr9:112800-113400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
31	chr9:112800-113400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
32	chr9:112800-113400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
33	chr9:112800-113400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
34	chr9:112800-113400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr9:112800-113400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr9:112800-113400	Bivalent Enhancer	Adipose Nuclei	Adipose
37	chr9:112800-113400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
38	chr9:112800-113400	Bivalent/Poised TSS	Right Ventricle	heart
39	chr9:112800-113400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
40	chr9:112800-113600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
41	chr9:112800-113600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr9:112800-113800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
43	chr9:112800-113800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
44	chr9:112800-114000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
45	chr9:112800-115200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
46	chr9:112800-115400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
47	chr9:113000-113200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr9:113000-113200	Active TSS	Primary hematopoietic stem cells short term culture	blood
49	chr9:113000-113200	Bivalent Enhancer	Fetal Intestine Large	intestine
50	chr9:113000-113400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell

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