Variant report

Variant	nsv892003
Chromosome Location	chr9:822594-863635
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:247)
CpG islands
(count:916)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:247 , 50 per page) page: 1 2 3 4 5

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	ATF2	chr9:859161-859692	GM12878	blood:	n/a	n/a
3	ATF2	chr9:859288-859680	GM12878	blood:	n/a	n/a
4	BACH1	chr9:841437-841715	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr9:847470-847844	GM12878	blood:	n/a	n/a
6	BATF	chr9:847504-847840	GM12878	blood:	n/a	n/a
7	BCL11A	chr9:859287-859598	GM12878	blood:	n/a	n/a
8	BCL11A	chr9:859277-859643	GM12878	blood:	n/a	n/a
9	BCL11A	chr9:840410-840568	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr9:852632-852864	GM12878	blood:	n/a	n/a
11	BHLHE40	chr9:859004-859714	GM12878	blood:	n/a	n/a
12	CEBPB	chr9:836594-836631	HepG2	liver:	n/a	chr9:836599-836610
13	CEBPB	chr9:838394-838547	MCF-7	breast:	n/a	chr9:838455-838466
14	CEBPB	chr9:856522-856717	A549	lung:	n/a	n/a
15	CEBPB	chr9:838431-838470	HepG2	liver:	n/a	chr9:838455-838466
16	CHD2	chr9:859215-859672	GM12878	blood:	n/a	n/a
17	CHD2	chr9:826666-826799	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr9:852634-852834	GM12878	blood:	n/a	n/a
19	CREB1	chr9:843173-843475	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTBP2	chr9:840294-840738	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr9:841342-842260	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr9:842540-843394	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr9:847040-847190	HCT-116	colon:	n/a	n/a
24	CTCF	chr9:830221-830241	LNCaP	prostate:	n/a	n/a
25	CTCF	chr9:826569-826889	H1-hESC	embryonic stem cell:	n/a	chr9:826760-826776
26	CTCF	chr9:826694-826820	MCF-7	breast:	n/a	chr9:826760-826776
27	CTCF	chr9:840460-840610	HRPEpiC	eye:	n/a	chr9:840475-840488
28	CTCF	chr9:840381-840550	HepG2	liver:	n/a	chr9:840475-840488
29	CTCF	chr9:840360-840510	HRE	kidney:	n/a	chr9:840475-840488
30	CTCF	chr9:826679-826824	MCF-7	breast:	n/a	chr9:826760-826776
31	CTCF	chr9:840460-840610	HCM	heart:	n/a	chr9:840475-840488
32	CTCF	chr9:847080-847230	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr9:840540-840690	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr9:847020-847170	GM12870	blood:	n/a	n/a
35	CTCF	chr9:826669-826858	H1-hESC	embryonic stem cell:	n/a	chr9:826760-826776
36	CTCF	chr9:840400-840550	GM12878	blood:	n/a	chr9:840475-840488
37	CTCF	chr9:847123-847143	MCF-7	breast:	n/a	n/a
38	CTCF	chr9:832625-832690	GM10248	blood:	n/a	n/a
39	CTCF	chr9:847082-847184	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr9:863320-863470	GM12875	blood:	n/a	n/a
41	CTCF	chr9:847065-847132	MCF-7	breast:	n/a	n/a
42	CTCF	chr9:841760-841910	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr9:840360-840510	HRPEpiC	eye:	n/a	chr9:840475-840488
44	CTCF	chr9:826749-826783	NHEK	skin:	n/a	chr9:826760-826776
45	CTCF	chr9:847020-847170	HepG2	liver:	n/a	n/a
46	CTCF	chr9:840434-840492	HUVEC	blood vessel:	n/a	chr9:840475-840488
47	CTCF	chr9:847060-847210	GM12875	blood:	n/a	n/a
48	CTCF	chr9:840340-840490	HCT-116	colon:	n/a	chr9:840475-840488
49	CTCF	chr9:847080-847230	GM12866	blood:	n/a	n/a
50	CTCF	chr9:847080-847230	GM12875	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:842799-842849	AG10803	skin:	n/a
2	chr9:842799-842849	AG10803	skin:	n/a
3	chr9:841632-841682	U87	brain:	n/a
4	chr9:839126-839176	PFSK-1	brain:	n/a
5	chr9:841636-841686	SAEC	small airway:	n/a
6	chr9:857563-857613	MCF10A-Er-Src	breast:	n/a
7	chr9:842914-842964	GM12878	blood:	n/a
8	chr9:845427-845477	HRE	kidney:	n/a
9	chr9:841850-841900	Jurkat	blood:	n/a
10	chr9:841436-841486	T-47D	breast:	n/a
11	chr9:843748-843798	MCF10A-Er-Src	breast:	n/a
12	chr9:841632-841682	IMR90	lung:	fetal
13	chr9:843179-843229	RPTEC	kidney:	n/a
14	chr9:841340-841390	IMR90	lung:	fetal
15	chr9:826657-826707	GM12892	blood:	n/a
16	chr9:845427-845477	HCPEpiC	choroid plexus:	n/a
17	chr9:841559-841609	AG09309	skin:	n/a
18	chr9:841340-841390	NHDF-neo	bronchial:	n/a
19	chr9:843748-843798	HepG2	liver:	n/a
20	chr9:842799-842849	BE2_C	brain:	n/a
21	chr9:843748-843798	GM12891	blood:	n/a
22	chr9:843179-843229	PFSK-1	brain:	n/a
23	chr9:841436-841486	HCF	heart:	n/a
24	chr9:842799-842849	AG09319	gingival:	n/a
25	chr9:841340-841390	NB4	blood:	n/a
26	chr9:841850-841900	HEK293	kidney:	embryo
27	chr9:826657-826707	SK-N-SH	brain:	n/a
28	chr9:857563-857613	HCT-116	colon:	n/a
29	chr9:841559-841609	PFSK-1	brain:	n/a
30	chr9:839557-839607	ovcar-3	ovarian:	n/a
31	chr9:845427-845477	HepG2	liver:	n/a
32	chr9:841436-841486	NHBE	bronchial:	n/a
33	chr9:841850-841900	AG09309	skin:	n/a
34	chr9:841559-841609	T-47D	breast:	n/a
35	chr9:843179-843229	HCPEpiC	choroid plexus:	n/a
36	chr9:839126-839176	HRE	kidney:	n/a
37	chr9:841436-841486	A549	lung:	n/a
38	chr9:842799-842849	PANC-1	pancreas:	n/a
39	chr9:857563-857613	CMK	blood:	n/a
40	chr9:843179-843229	Hepatocyte	liver:	n/a
41	chr9:841850-841900	T-47D	breast:	n/a
42	chr9:826657-826707	AG09309	skin:	n/a
43	chr9:839557-839607	PrEC	prostate:	n/a
44	chr9:843748-843798	HCT-116	colon:	n/a
45	chr9:841436-841486	HRPEpiC	eye:	n/a
46	chr9:843748-843798	Hela-S3	cervix:	n/a
47	chr9:839126-839176	Hepatocyte	liver:	n/a
48	chr9:845427-845477	MCF10A-Er-Src	breast:	n/a
49	chr9:839557-839607	SK-N-SH	brain:	n/a
50	chr9:841559-841609	AoSMC	blood vessel:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:829461..831177-chr9:832230..834782,2	MCF-7	breast:
2	chr9:826413..827016-chr9:1004866..1005745,2	MCF-7	breast:
3	chr9:852085..854136-chr9:910104..912950,2	K562	blood:
4	chr9:843269..845393-chr9:851272..854140,2	MCF-7	breast:
5	chr9:829461..831177-chr9:832230..834782,2	MCF-7	breast:
6	chr9:858181..863479-chr9:867333..871768,4	MCF-7	breast:
7	chr9:846543..848941-chr9:858349..860587,2	K562	blood:
8	chr9:843269..845393-chr9:851272..854140,2	MCF-7	breast:
9	chr9:845876..848526-chr9:868544..871068,2	MCF-7	breast:
10	chr9:846543..848941-chr9:858349..860587,2	K562	blood:

No data

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

Extended variants
information (count: 1389 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:1389 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10976813	chr9:825647-825648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547889508	chr9:825677-825678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528516528	chr9:825681-825682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376003545	chr9:825684-825685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568612354	chr9:825686-825687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537540007	chr9:825705-825706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201429117	chr9:825727-825728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150733092	chr9:825730-825731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370281124	chr9:825736-825737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141247406	chr9:825752-825753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571036414	chr9:825760-825761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557108390	chr9:825794-825795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533262225	chr9:826418-826419	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs374148569	chr9:826419-826420	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs10976818	chr9:826427-826428	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs151118221	chr9:826429-826430	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs535617985	chr9:826450-826451	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs549287898	chr9:826451-826452	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs569185629	chr9:826475-826476	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs184195968	chr9:826525-826526	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs556675477	chr9:826527-826528	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs555922403	chr9:826536-826537	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs142594144	chr9:826540-826541	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs11794700	chr9:826561-826562	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs553437589	chr9:826565-826566	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs573092645	chr9:826570-826571	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs199772280	chr9:826584-826585	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs368084273	chr9:826585-826586	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs575599826	chr9:826595-826596	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs544638242	chr9:826603-826604	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs534691091	chr9:826611-826612	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs369256665	chr9:826621-826622	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs190643240	chr9:826631-826632	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs533317174	chr9:826652-826653	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs72697172	chr9:826653-826654	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs4742449	chr9:826656-826657	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs139000811	chr9:826661-826662	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs4742450	chr9:826701-826702	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs549150662	chr9:826709-826710	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs80099296	chr9:826726-826727	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs181942776	chr9:826728-826729	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs569422953	chr9:826737-826738	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs552006228	chr9:826744-826745	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs570363854	chr9:826754-826755	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs539388011	chr9:826755-826756	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs10125000	chr9:826794-826795	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs73639429	chr9:826796-826797	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs74324459	chr9:826856-826857	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs10114044	chr9:826878-826879	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs372412230	chr9:826915-826916	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:825600-825800	Enhancers	HMEC	breast
2	chr9:826400-826800	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr9:826600-827200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:827000-827800	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr9:833400-833800	Enhancers	Aorta	Aorta
6	chr9:837600-837800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:840000-841800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:840200-840400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
9	chr9:840200-840400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
10	chr9:840200-840400	Bivalent Enhancer	Fetal Thymus	thymus
11	chr9:840200-840600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
12	chr9:840200-841000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
13	chr9:840200-841000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
14	chr9:840200-841200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
15	chr9:840200-841200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
16	chr9:840400-840600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
17	chr9:840400-840800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr9:840400-840800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr9:840400-840800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
20	chr9:840400-841600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr9:840600-840800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr9:840600-840800	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr9:840600-841000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr9:840600-841000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
25	chr9:840600-841000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr9:840600-841600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr9:840800-841000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
28	chr9:840800-841400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
29	chr9:841000-841200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
30	chr9:841000-841200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
31	chr9:841000-841400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr9:841000-841600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
33	chr9:841000-843400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
34	chr9:841200-841400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
35	chr9:841200-841400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
36	chr9:841200-841400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr9:841200-841400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr9:841200-841400	Bivalent Enhancer	Fetal Thymus	thymus
39	chr9:841200-841600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
40	chr9:841200-841600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr9:841200-841600	Flanking Bivalent TSS/Enh	A549	lung
42	chr9:841200-841800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr9:841200-841800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
44	chr9:841200-841800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr9:841200-842000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
46	chr9:841200-842400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr9:841200-843200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
48	chr9:841200-843200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr9:841200-843200	Bivalent Enhancer	Liver	Liver
50	chr9:841200-843400	Bivalent Enhancer	Fetal Muscle Leg	muscle

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