Variant report

Variant	nsv892005
Chromosome Location	chr9:832711-853004
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:145)
CpG islands
(count:793)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:145 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:840342-840725	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr9:841437-841715	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr9:847504-847840	GM12878	blood:	n/a	n/a
4	BATF	chr9:847470-847844	GM12878	blood:	n/a	n/a
5	BCL11A	chr9:840410-840568	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr9:852632-852864	GM12878	blood:	n/a	n/a
7	CEBPB	chr9:838431-838470	HepG2	liver:	n/a	chr9:838455-838466
8	CEBPB	chr9:836594-836631	HepG2	liver:	n/a	chr9:836599-836610
9	CEBPB	chr9:838394-838547	MCF-7	breast:	n/a	chr9:838455-838466
10	CHD2	chr9:852634-852834	GM12878	blood:	n/a	n/a
11	CREB1	chr9:843173-843475	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTBP2	chr9:842540-843394	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTBP2	chr9:841342-842260	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTBP2	chr9:840294-840738	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr9:847080-847230	GM12866	blood:	n/a	n/a
16	CTCF	chr9:840434-840492	HUVEC	blood vessel:	n/a	chr9:840475-840488
17	CTCF	chr9:847060-847210	HEK293	kidney:	n/a	n/a
18	CTCF	chr9:847080-847230	GM12875	blood:	n/a	n/a
19	CTCF	chr9:847080-847230	MCF-7	breast:	n/a	n/a
20	CTCF	chr9:847060-847210	GM12865	blood:	n/a	n/a
21	CTCF	chr9:847120-847270	NHEK	skin:	n/a	n/a
22	CTCF	chr9:841760-841910	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr9:841719-841807	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr9:851460-851610	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr9:840460-840610	HRPEpiC	eye:	n/a	chr9:840475-840488
26	CTCF	chr9:847065-847132	MCF-7	breast:	n/a	n/a
27	CTCF	chr9:847082-847184	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr9:847020-847170	HepG2	liver:	n/a	n/a
29	CTCF	chr9:840540-840690	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr9:840381-840550	HepG2	liver:	n/a	chr9:840475-840488
31	CTCF	chr9:840360-840510	HRPEpiC	eye:	n/a	chr9:840475-840488
32	CTCF	chr9:840400-840550	GM12878	blood:	n/a	chr9:840475-840488
33	CTCF	chr9:847123-847143	MCF-7	breast:	n/a	n/a
34	CTCF	chr9:847080-847230	GM12874	blood:	n/a	n/a
35	CTCF	chr9:840340-840490	HCT-116	colon:	n/a	chr9:840475-840488
36	CTCF	chr9:847020-847170	GM12870	blood:	n/a	n/a
37	CTCF	chr9:840460-840610	HCM	heart:	n/a	chr9:840475-840488
38	CTCF	chr9:847080-847230	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr9:841680-841830	GM06990	blood:	n/a	chr9:841706-841719
40	CTCF	chr9:847020-847170	MCF-7	breast:	n/a	n/a
41	CTCF	chr9:847040-847190	HCT-116	colon:	n/a	n/a
42	CTCF	chr9:840470-840492	HepG2	liver:	n/a	chr9:840475-840488
43	CTCF	chr9:840500-840650	HepG2	liver:	n/a	n/a
44	CTCF	chr9:840360-840510	HRE	kidney:	n/a	chr9:840475-840488
45	CTCF	chr9:846960-847110	GM12867	blood:	n/a	n/a
46	CTCF	chr9:847040-847190	GM12871	blood:	n/a	n/a
47	CTCF	chr9:840440-840590	HBMEC	blood vessel:	n/a	chr9:840475-840488
48	CTCF	chr9:847060-847210	GM12875	blood:	n/a	n/a
49	CTCF	chr9:846980-847130	GM12872	blood:	n/a	n/a
50	E2F6	chr9:842447-842856	H1-hESC	embryonic stem cell:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:841559-841609	GM12891	blood:	n/a
2	chr9:842799-842849	HMEC	breast:	n/a
3	chr9:841636-841686	MCF10A-Er-Src	breast:	n/a
4	chr9:839126-839176	HUVEC	blood vessel:	n/a
5	chr9:841636-841686	AG09309	skin:	n/a
6	chr9:841850-841900	NHDF-neo	bronchial:	n/a
7	chr9:845427-845477	MCF10A-Er-Src	breast:	n/a
8	chr9:841636-841686	HCT-116	colon:	n/a
9	chr9:841436-841486	HCT-116	colon:	n/a
10	chr9:839126-839176	GM12891	blood:	n/a
11	chr9:839126-839176	SK-N-SH	brain:	n/a
12	chr9:845427-845477	NHBE	bronchial:	n/a
13	chr9:841636-841686	PFSK-1	brain:	n/a
14	chr9:839557-839607	Jurkat	blood:	n/a
15	chr9:843748-843798	GM12892	blood:	n/a
16	chr9:841636-841686	NB4	blood:	n/a
17	chr9:841340-841390	SK-N-MC	brain:	n/a
18	chr9:841340-841390	T-47D	breast:	n/a
19	chr9:841340-841390	Hepatocyte	liver:	n/a
20	chr9:841559-841609	GM12878	blood:	n/a
21	chr9:841632-841682	MCF-7	breast:	n/a
22	chr9:842799-842849	HNPCEpiC	eye:	n/a
23	chr9:839557-839607	HIPEpiC	eye:	n/a
24	chr9:842914-842964	NHDF-neo	bronchial:	n/a
25	chr9:843179-843229	T-47D	breast:	n/a
26	chr9:843179-843229	HCT-116	colon:	n/a
27	chr9:843748-843798	ovcar-3	ovarian:	n/a
28	chr9:839557-839607	ovcar-3	ovarian:	n/a
29	chr9:841436-841486	AG09319	gingival:	n/a
30	chr9:842914-842964	NT2-D1	testis:	n/a
31	chr9:845427-845477	NH-A	brain:	n/a
32	chr9:841340-841390	HepG2	liver:	n/a
33	chr9:841436-841486	GM06990	blood:	n/a
34	chr9:841636-841686	RPTEC	kidney:	n/a
35	chr9:842799-842849	HL-60	blood:	n/a
36	chr9:841636-841686	HMEC	breast:	n/a
37	chr9:843748-843798	GM06990	blood:	n/a
38	chr9:841636-841686	HUVEC	blood vessel:	n/a
39	chr9:839557-839607	HMEC	breast:	n/a
40	chr9:843748-843798	AG10803	skin:	n/a
41	chr9:839557-839607	HAEpiC	amniotic membrane:	n/a
42	chr9:839557-839607	CMK	blood:	n/a
43	chr9:841850-841900	SAEC	small airway:	n/a
44	chr9:841632-841682	SK-N-SH_RA	brain:	n/a
45	chr9:845427-845477	HEK293	kidney:	embryo
46	chr9:841436-841486	U87	brain:	n/a
47	chr9:839126-839176	PFSK-1	brain:	n/a
48	chr9:842799-842849	SK-N-SH_RA	brain:	n/a
49	chr9:841340-841390	SK-N-SH	brain:	n/a
50	chr9:841340-841390	PrEC	prostate:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:852085..854136-chr9:910104..912950,2	K562	blood:
2	chr9:843269..845393-chr9:851272..854140,2	MCF-7	breast:
3	chr9:829461..831177-chr9:832230..834782,2	MCF-7	breast:
4	chr9:846543..848941-chr9:858349..860587,2	K562	blood:
5	chr9:843269..845393-chr9:851272..854140,2	MCF-7	breast:
6	chr9:845876..848526-chr9:868544..871068,2	MCF-7	breast:

No data

Variant related genes	Relation type
DMRT1	TF binding region
DMRT1	CpG island

Extended variants
information (count: 769 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:769 , 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	rs532682454	chr9:833400-833401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191494746	chr9:833416-833417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539008195	chr9:833437-833438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566095558	chr9:833449-833450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368049081	chr9:833455-833456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535294793	chr9:833499-833500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148873283	chr9:833507-833508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143618846	chr9:833539-833540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182241001	chr9:833551-833552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148059906	chr9:833553-833554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs118180754	chr9:833570-833571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186627671	chr9:833574-833575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538365790	chr9:833584-833585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558093321	chr9:833607-833608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140745666	chr9:833615-833616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541070514	chr9:833635-833636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561019046	chr9:833650-833651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574711068	chr9:833652-833653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543231177	chr9:833655-833656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552689412	chr9:833680-833681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192711177	chr9:833683-833684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115709978	chr9:833694-833695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145724711	chr9:833707-833708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs16924644	chr9:833708-833709	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs185480345	chr9:833715-833716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188785144	chr9:833729-833730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10815800	chr9:833740-833741	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs117493483	chr9:833745-833746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs60448411	chr9:833755-833756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570725385	chr9:833757-833758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138726899	chr9:833792-833793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192223803	chr9:837613-837614	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs565678144	chr9:837657-837658	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs534598831	chr9:837700-837701	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs547908301	chr9:837701-837702	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs568335830	chr9:837703-837704	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs182936894	chr9:837715-837716	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs55946147	chr9:837721-837722	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs577111855	chr9:837733-837734	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs61571667	chr9:837765-837766	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs12337483	chr9:837775-837776	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs7854211	chr9:838395-838396	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs34202154	chr9:838396-838397	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs112415972	chr9:838414-838415	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs7860095	chr9:838422-838423	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs571956468	chr9:838436-838437	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs574146969	chr9:838460-838461	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs138475406	chr9:838461-838462	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs561748031	chr9:838464-838465	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs189449446	chr9:838471-838472	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	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
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
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	21272361	CNVD
Ependymoma	20639864	CNVD
Non-small cell lung cancer	16651412	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:219 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:833400-833800	Enhancers	Aorta	Aorta
2	chr9:837600-837800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:840000-841800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:840200-840400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
5	chr9:840200-840400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
6	chr9:840200-840400	Bivalent Enhancer	Fetal Thymus	thymus
7	chr9:840200-840600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
8	chr9:840200-841000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
9	chr9:840200-841000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
10	chr9:840200-841200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
11	chr9:840200-841200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
12	chr9:840400-840600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
13	chr9:840400-840800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:840400-840800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:840400-840800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
16	chr9:840400-841600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:840600-840800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr9:840600-840800	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr9:840600-841000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr9:840600-841000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
21	chr9:840600-841000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr9:840600-841600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr9:840800-841000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
24	chr9:840800-841400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
25	chr9:841000-841200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
26	chr9:841000-841200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
27	chr9:841000-841400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr9:841000-841600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
29	chr9:841000-843400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
30	chr9:841200-841400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
31	chr9:841200-841400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
32	chr9:841200-841400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr9:841200-841400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr9:841200-841400	Bivalent Enhancer	Fetal Thymus	thymus
35	chr9:841200-841600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
36	chr9:841200-841600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr9:841200-841600	Flanking Bivalent TSS/Enh	A549	lung
38	chr9:841200-841800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr9:841200-841800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
40	chr9:841200-841800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr9:841200-842000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
42	chr9:841200-842400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr9:841200-843200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
44	chr9:841200-843200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr9:841200-843200	Bivalent Enhancer	Liver	Liver
46	chr9:841200-843400	Bivalent Enhancer	Fetal Muscle Leg	muscle
47	chr9:841200-843400	Bivalent Enhancer	Placenta	Placenta
48	chr9:841400-841600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
49	chr9:841400-841600	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr9:841400-841600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum

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