Variant report

Variant	nsv615641
Chromosome Location	chr9:136525306-136534031
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	chr9:136529921-136529986	LNCaP	prostate:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
2	CTCF	chr9:136529945-136529976	HUVEC	blood vessel:	n/a	chr9:136529963-136529976
3	CTCF	chr9:136529959-136530025	Lung_OC	lung:	n/a	chr9:136529963-136529976
4	CTCF	chr9:136529880-136530030	BE2_C	brain:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
5	CTCF	chr9:136529911-136530055	NHEK	skin:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
6	CTCF	chr9:136529920-136530070	HA-sp	spinal cord:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
7	CTCF	chr9:136529877-136530077	GM12891	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
8	CTCF	chr9:136529820-136529970	HUVEC	blood vessel:	n/a	chr9:136529939-136529947
9	CTCF	chr9:136529920-136530070	SAEC	small airway:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
10	CTCF	chr9:136529900-136530050	HCPEpiC	choroid plexus:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
11	CTCF	chr9:136529899-136530058	GM10248	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
12	CTCF	chr9:136529914-136530003	GM20000	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
13	CTCF	chr9:136529880-136530030	GM12875	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
14	CTCF	chr9:136529920-136530070	GM12871	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
15	CTCF	chr9:136529840-136529990	HCFaa	heart:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
16	CTCF	chr9:136529860-136530010	MCF-7	breast:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
17	CTCF	chr9:136529900-136530050	Hela-S3	cervix:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
18	CTCF	chr9:136529889-136530006	SK-N-SH_RA	brain:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
19	CTCF	chr9:136529900-136530050	HepG2	liver:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
20	CTCF	chr9:136530000-136530150	GM12868	blood:	n/a	n/a
21	CTCF	chr9:136529881-136530027	GM12878	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
22	CTCF	chr9:136529955-136530017	GM13977	blood:	n/a	chr9:136529963-136529976
23	CTCF	chr9:136529931-136530026	A549	lung:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
24	CTCF	chr9:136529860-136530010	RPTEC	kidney:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
25	CTCF	chr9:136529940-136530090	GM12872	blood:	n/a	chr9:136529963-136529976
26	CTCF	chr9:136529900-136530050	GM06990	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
27	CTCF	chr9:136529880-136530081	GM12892	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
28	CTCF	chr9:136529880-136530030	HCPEpiC	choroid plexus:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
29	CTCF	chr9:136529920-136530070	MCF-7	breast:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
30	CTCF	chr9:136529941-136530039	GM19239	blood:	n/a	chr9:136529963-136529976
31	CTCF	chr9:136529900-136530050	Caco-2	colon:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
32	CTCF	chr9:136529840-136530130	GM12866	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
33	CTCF	chr9:136529942-136529989	HepG2	liver:	n/a	chr9:136529963-136529976
34	CTCF	chr9:136529891-136529925	K562	blood:	n/a	n/a
35	CTCF	chr9:136529880-136530030	HEK293	kidney:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
36	CTCF	chr9:136529920-136530070	SK-N-SH_RA	brain:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
37	CTCF	chr9:136529940-136530090	HFF-Myc	foreskin:	n/a	chr9:136529963-136529976
38	CTCF	chr9:136529906-136530079	H1-hESC	embryonic stem cell:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
39	CTCF	chr9:136529954-136530070	GM10266	blood:	n/a	chr9:136529963-136529976
40	CTCF	chr9:136529900-136530050	HPAF	blood vessel:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
41	CTCF	chr9:136529860-136530010	HCM	heart:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
42	CTCF	chr9:136529860-136530010	HEK293	kidney:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
43	CTCF	chr9:136529863-136530100	MCF-7	breast:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
44	CTCF	chr9:136529940-136530090	HCT-116	colon:	n/a	chr9:136529963-136529976
45	CTCF	chr9:136529900-136530050	HBMEC	blood vessel:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
46	CTCF	chr9:136529860-136530010	AG09309	skin:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
47	CTCF	chr9:136529940-136530090	HA-sp	spinal cord:	n/a	chr9:136529963-136529976
48	CTCF	chr9:136529880-136530030	HVMF	connective:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
49	CTCF	chr9:136529872-136530089	MCF-7	breast:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
50	CTCF	chr9:136529860-136530010	HAc	cerebellar:	n/a	chr9:136529963-136529976 chr9:136529939-136529947

No.	Distal block	Cell Line	Cell type
1	chr9:136397976..136398826-chr9:136528405..136529390,2	MCF-7	breast:
2	chr9:136492846..136495441-chr9:136522709..136525633,2	MCF-7	breast:
3	chr9:136524956..136527895-chr9:136529322..136531931,3	MCF-7	breast:
4	chr9:136524956..136527895-chr9:136529322..136531931,3	MCF-7	breast:
5	chr9:136528592..136530737-chr9:136533318..136534835,2	K562	blood:
6	chr9:136518974..136520647-chr9:136523004..136525968,2	K562	blood:
7	chr9:136520134..136522462-chr9:136523738..136526239,2	MCF-7	breast:
8	chr9:136528562..136531390-chr9:136533335..136537164,3	K562	blood:
9	chr9:136406344..136408415-chr9:136524304..136526688,2	MCF-7	breast:
10	chr9:136528562..136531390-chr9:136533335..136537164,3	K562	blood:
11	chr9:136533491..136538951-chr9:136540367..136544630,5	MCF-7	breast:
12	chr9:136523144..136526065-chr9:136527921..136530216,2	MCF-7	breast:
13	chr9:136528532..136530062-chr9:136535645..136537164,2	K562	blood:
14	chr9:136518974..136521399-chr9:136523004..136525968,3	K562	blood:
15	chr9:136523144..136526065-chr9:136527921..136530216,2	MCF-7	breast:
16	chr9:136528592..136530737-chr9:136533318..136534835,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM163B-2	chr9:136529094-136529136	NONHSAT135335
2	lnc-FAM163B-2	chr9:136531857-136532245	NONHSAT135335

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

Extended variants
information (count: 463 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs129919	chr9:136525306-136525307	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541366303	chr9:136525314-136525315	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs555115912	chr9:136525339-136525340	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573244154	chr9:136525343-136525344	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs34770100	chr9:136525362-136525363	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs558951613	chr9:136525366-136525367	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577153884	chr9:136525373-136525374	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs569124535	chr9:136525409-136525410	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs370221965	chr9:136525411-136525412	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs60646488	chr9:136525422-136525423	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs544933061	chr9:136525465-136525466	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs563216970	chr9:136525471-136525472	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs575115036	chr9:136525474-136525475	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs184445884	chr9:136525486-136525487	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs555337613	chr9:136525525-136525526	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs543796346	chr9:136525535-136525536	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs528234587	chr9:136525569-136525570	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs546366646	chr9:136525599-136525600	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs564927162	chr9:136525651-136525652	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs397835174	chr9:136525653-136525654	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs129920	chr9:136525654-136525655	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs116807965	chr9:136525757-136525758	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs144649112	chr9:136525863-136525864	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs201921566	chr9:136525873-136525874	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs536846291	chr9:136525918-136525919	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs548848256	chr9:136525945-136525946	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs182442868	chr9:136525973-136525974	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs10993950	chr9:136525988-136525989	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs187006750	chr9:136526011-136526012	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs577192938	chr9:136526046-136526047	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs191029452	chr9:136526097-136526098	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs556848115	chr9:136526119-136526120	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs575151273	chr9:136526187-136526188	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs542508251	chr9:136526188-136526189	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs180819543	chr9:136526189-136526190	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs148047312	chr9:136526190-136526191	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs141632920	chr9:136526199-136526200	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs374471354	chr9:136526233-136526234	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs564799284	chr9:136526251-136526252	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs563867077	chr9:136526259-136526260	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs532148653	chr9:136526264-136526265	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs571957958	chr9:136526291-136526292	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs147130976	chr9:136526332-136526333	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs534217846	chr9:136526334-136526335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4979629	chr9:136526388-136526389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530458530	chr9:136526407-136526408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529458232	chr9:136526438-136526439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564270092	chr9:136526442-136526443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548884954	chr9:136526466-136526467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111422860	chr9:136526469-136526470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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	17122850	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136520400-136525800	Enhancers	Primary T helper cells PMA-I stimulated	--
2	chr9:136521000-136526600	Enhancers	Liver	Liver
3	chr9:136522400-136525400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
4	chr9:136522400-136526000	Bivalent Enhancer	Fetal Thymus	thymus
5	chr9:136523000-136525400	Enhancers	Primary T cells from cord blood	blood
6	chr9:136523600-136525400	Enhancers	Esophagus	oesophagus
7	chr9:136524000-136526000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:136524400-136525400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
9	chr9:136524400-136525400	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
10	chr9:136524400-136527800	Weak transcription	Ovary	ovary
11	chr9:136524400-136541200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr9:136524600-136528800	Weak transcription	Spleen	Spleen
13	chr9:136524600-136530800	Weak transcription	Lung	lung
14	chr9:136524800-136525400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr9:136524800-136535600	Weak transcription	HepG2	liver
16	chr9:136524800-136537000	Weak transcription	Fetal Lung	lung
17	chr9:136524800-136542800	Weak transcription	Right Atrium	heart
18	chr9:136524800-136555600	Weak transcription	HSMM	muscle
19	chr9:136525000-136525400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
20	chr9:136525000-136527800	Weak transcription	Pancreas	Pancrea
21	chr9:136525000-136530800	Weak transcription	Brain Germinal Matrix	brain
22	chr9:136525000-136556800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr9:136525200-136525600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr9:136525200-136526000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:136525200-136527800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr9:136525200-136531000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr9:136525200-136534000	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr9:136525200-136534600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr9:136525400-136525600	Enhancers	Primary hematopoietic stem cells	blood
30	chr9:136525400-136528600	Weak transcription	Primary T cells from cord blood	blood
31	chr9:136525400-136534600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr9:136525800-136526000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr9:136525800-136536200	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr9:136526000-136527000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr9:136526000-136527000	Weak transcription	Fetal Stomach	stomach
36	chr9:136526000-136534400	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr9:136526000-136534800	Weak transcription	Fetal Intestine Small	intestine
38	chr9:136526200-136529800	Weak transcription	Thymus	Thymus
39	chr9:136526600-136527400	Weak transcription	Liver	Liver
40	chr9:136527000-136527200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr9:136527000-136527200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
42	chr9:136527000-136528000	Enhancers	Fetal Thymus	thymus
43	chr9:136527000-136528200	Enhancers	Fetal Muscle Leg	muscle
44	chr9:136527000-136528400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr9:136527000-136529800	Strong transcription	Fetal Stomach	stomach
46	chr9:136527200-136527400	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr9:136527200-136527400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr9:136527200-136528200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:136527400-136527600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr9:136527400-136527600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland

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