Variant report

Variant	nsv1038487
Chromosome Location	chr9:140746220-140875798
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1276)
CpG islands
(count:1405)
Chromatin interactive
region (count:36)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1276 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:140761215-140761514	GM12878	blood:	n/a	n/a
2	ATF3	chr9:140851195-140851422	K562	blood:	n/a	n/a
3	ATF3	chr9:140772100-140772314	K562	blood:	n/a	chr9:140772176-140772196
4	ATF3	chr9:140772113-140772351	H1-hESC	embryonic stem cell:	n/a	chr9:140772176-140772196
5	BACH1	chr9:140778170-140778249	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:140773050-140773062	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr9:140747930-140748125	GM12878	blood:	n/a	n/a
8	BATF	chr9:140761031-140761428	GM12878	blood:	n/a	n/a
9	BATF	chr9:140768772-140769151	GM12878	blood:	n/a	n/a
10	BATF	chr9:140768794-140769134	GM12878	blood:	n/a	n/a
11	BCL11A	chr9:140768831-140769188	GM12878	blood:	n/a	n/a
12	BCL11A	chr9:140761035-140761355	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:140768767-140769277	GM12878	blood:	n/a	n/a
14	BCL3	chr9:140760724-140761478	GM12878	blood:	n/a	n/a
15	BHLHE40	chr9:140760778-140760955	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:140851159-140851515	K562	blood:	n/a	n/a
17	BHLHE40	chr9:140772955-140773232	K562	blood:	n/a	chr9:140773100-140773109
18	BHLHE40	chr9:140761159-140761359	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:140862896-140863013	K562	blood:	n/a	n/a
20	BHLHE40	chr9:140851209-140851501	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:140851240-140851513	HepG2	liver:	n/a	n/a
22	BHLHE40	chr9:140782765-140782847	K562	blood:	n/a	n/a
23	BRCA1	chr9:140841105-140841139	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr9:140761625-140761775	GM12878	blood:	n/a	n/a
25	CBX3	chr9:140778966-140779313	K562	blood:	n/a	n/a
26	CBX3	chr9:140851178-140851459	K562	blood:	n/a	n/a
27	CBX3	chr9:140839953-140840442	HCT-116	colon:	n/a	n/a
28	CCNT2	chr9:140773119-140773339	K562	blood:	n/a	chr9:140773196-140773205
29	CEBPB	chr9:140746402-140746765	MCF-7	breast:	n/a	n/a
30	CEBPB	chr9:140761024-140761478	GM12878	blood:	n/a	n/a
31	CEBPB	chr9:140768431-140768772	K562	blood:	n/a	n/a
32	CEBPB	chr9:140746103-140746326	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:140746423-140746547	A549	lung:	n/a	n/a
34	CEBPB	chr9:140746440-140746708	K562	blood:	n/a	n/a
35	CEBPB	chr9:140779145-140779214	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr9:140745962-140746844	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr9:140768460-140768776	Hela-S3	cervix:	n/a	n/a
38	CEBPZ	chr9:140840083-140840374	HepG2	liver:	n/a	n/a
39	CHD2	chr9:140779562-140779722	HepG2	liver:	n/a	n/a
40	CHD2	chr9:140785342-140785646	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr9:140783738-140783742	HepG2	liver:	n/a	n/a
42	CHD2	chr9:140773087-140773408	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr9:140785425-140785454	K562	blood:	n/a	n/a
44	CHD2	chr9:140784054-140784072	HepG2	liver:	n/a	n/a
45	CTBP2	chr9:140773019-140773492	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr9:140855140-140855290	GM12878	blood:	n/a	n/a
47	CTCF	chr9:140773079-140773266	HepG2	liver:	n/a	n/a
48	CTCF	chr9:140779040-140779190	MCF-7	breast:	n/a	n/a
49	CTCF	chr9:140778060-140778210	HEK293	kidney:	n/a	n/a
50	CTCF	chr9:140779933-140780063	GM19240	blood:	n/a	chr9:140780009-140780022

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140775967-140776017	T-47D	breast:	n/a
2	chr9:140814587-140814637	PrEC	prostate:	n/a
3	chr9:140775967-140776017	T-47D	breast:	n/a
4	chr9:140814587-140814637	PrEC	prostate:	n/a
5	chr9:140780551-140780601	HIPEpiC	eye:	n/a
6	chr9:140771599-140771649	RPTEC	kidney:	n/a
7	chr9:140787445-140787495	SAEC	small airway:	n/a
8	chr9:140771599-140771649	AG04450	lung:	fetal
9	chr9:140775967-140776017	HRE	kidney:	n/a
10	chr9:140777406-140777456	Caco-2	colon:	n/a
11	chr9:140787445-140787495	ovcar-3	ovarian:	n/a
12	chr9:140816336-140816386	Hela-S3	cervix:	n/a
13	chr9:140771180-140771230	AG09319	gingival:	n/a
14	chr9:140773147-140773197	PFSK-1	brain:	n/a
15	chr9:140773129-140773179	K562	blood:	n/a
16	chr9:140780551-140780601	NH-A	brain:	n/a
17	chr9:140773129-140773179	NHDF-neo	bronchial:	n/a
18	chr9:140773129-140773179	HEK293	kidney:	embryo
19	chr9:140770915-140770965	AG10803	skin:	n/a
20	chr9:140771180-140771230	HRPEpiC	eye:	n/a
21	chr9:140850133-140850183	GM19239	blood:	n/a
22	chr9:140777406-140777456	AG04450	lung:	fetal
23	chr9:140816336-140816386	HRE	kidney:	n/a
24	chr9:140773147-140773197	CMK	blood:	n/a
25	chr9:140775041-140775091	AG09319	gingival:	n/a
26	chr9:140816336-140816386	HIPEpiC	eye:	n/a
27	chr9:140771990-140772040	HEEpiC	esophagus:	n/a
28	chr9:140814587-140814637	ProgFib	skin:	n/a
29	chr9:140778757-140778807	SAEC	small airway:	n/a
30	chr9:140773483-140773533	Jurkat	blood:	n/a
31	chr9:140770915-140770965	ProgFib	skin:	n/a
32	chr9:140771180-140771230	CMK	blood:	n/a
33	chr9:140815010-140815060	HPAEpiC	pulmonary alveolar:	n/a
34	chr9:140813541-140813591	Caco-2	colon:	n/a
35	chr9:140768247-140768297	K562	blood:	n/a
36	chr9:140775041-140775091	RPTEC	kidney:	n/a
37	chr9:140773129-140773179	A549	lung:	n/a
38	chr9:140787445-140787495	HRCEpiC	kidney:	n/a
39	chr9:140773147-140773197	HCT-116	colon:	n/a
40	chr9:140777406-140777456	GM12891	blood:	n/a
41	chr9:140850133-140850183	LNCaP	prostate:	n/a
42	chr9:140773129-140773179	AG09319	gingival:	n/a
43	chr9:140775967-140776017	GM06990	blood:	n/a
44	chr9:140772545-140772595	T-47D	breast:	n/a
45	chr9:140773147-140773197	PANC-1	pancreas:	n/a
46	chr9:140777406-140777456	ovcar-3	ovarian:	n/a
47	chr9:140773147-140773197	ovcar-3	ovarian:	n/a
48	chr9:140768247-140768297	HRCEpiC	kidney:	n/a
49	chr9:140777406-140777456	HRCEpiC	kidney:	n/a
50	chr9:140777406-140777456	GM12892	blood:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:149222900..149224638-chr9:140873623..140875123,3	MCF-7	breast:
2	chr9:140869140..140872298-chr9:140874733..140877130,3	MCF-7	breast:
3	chr9:140763820..140766702-chr9:140806866..140808617,2	K562	blood:
4	chr9:140471797..140473910-chr9:140767835..140770122,2	K562	blood:
5	chr9:140771023..140775053-chr9:140775846..140778577,6	MCF-7	breast:
6	chr9:140860566..140865150-chr9:140867846..140870803,4	MCF-7	breast:
7	chr9:140775069..140778564-chr9:140787877..140791721,3	MCF-7	breast:
8	chr9:140770577..140775862-chr9:140777147..140782162,8	K562	blood:
9	chr9:140778196..140781664-chr9:140782755..140784568,3	K562	blood:
10	chr9:140862016..140865668-chr9:140879753..140883106,4	MCF-7	breast:
11	chr9:140869140..140872298-chr9:140874733..140877130,3	MCF-7	breast:
12	chr9:140777999..140780667-chr9:140783373..140786900,7	MCF-7	breast:
13	chr9:140777999..140780667-chr9:140783373..140786900,7	MCF-7	breast:
14	chr9:140844057..140846982-chr9:140852715..140855154,2	MCF-7	breast:
15	chr1:149223801..149224429-chr9:140873103..140873623,7	MCF-7	breast:
16	chr9:140770577..140775397-chr9:140776407..140782162,11	K562	blood:
17	chr9:140797540..140799636-chr9:140804864..140807689,2	K562	blood:
18	chr9:140772539..140775418-chr9:140775684..140778164,5	MCF-7	breast:
19	chr1:149223037..149225339-chr9:140872123..140875123,7	MCF-7	breast:
20	chr9:140772539..140775418-chr9:140775684..140778164,5	MCF-7	breast:
21	chr9:140860566..140865150-chr9:140867846..140870803,4	MCF-7	breast:
22	chr9:140797540..140799636-chr9:140804864..140807689,2	K562	blood:
23	chr9:140763820..140766702-chr9:140806866..140808617,2	K562	blood:
24	chr9:140867124..140870002-chr9:140953480..140955243,2	MCF-7	breast:
25	chr9:140775069..140778564-chr9:140787877..140791721,3	MCF-7	breast:
26	chr9:140796431..140799040-chr9:140804864..140806682,2	K562	blood:
27	chr9:140865657..140867593-chr9:140877024..140879679,2	MCF-7	breast:
28	chr9:140864855..140867051-chr9:140878528..140880494,2	K562	blood:
29	chr14:100197709..100198229-chr9:140777193..140778054,2	MCF-7	breast:
30	chr9:140796431..140799040-chr9:140804864..140806682,2	K562	blood:
31	chr9:140841179..140843467-chr9:140845016..140846625,2	K562	blood:
32	chr9:140841179..140843467-chr9:140845016..140846625,2	K562	blood:
33	chr9:140778196..140781664-chr9:140782755..140784568,3	K562	blood:
34	chr1:149223401..149224369-chr9:140873101..140874123,8	MCF-7	breast:
35	chr9:140844057..140846982-chr9:140852715..140855154,2	MCF-7	breast:
36	chr9:140870732..140873052-chr9:140876120..140877929,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL772363.1-1	chr9:140768516-140768684	XLOC_007904
2	lnc-AL772363.1-1	chr9:140769915-140770132	ENSG00000203987.2
3	lnc-AL772363.1-1	chr9:140769915-140770844	XLOC_007904
4	lnc-AL772363.1-1	chr9:140777289-140777454	ENSG00000203987.2
5	lnc-AL772363.1-1	chr9:140784498-140787022	ENSG00000203987.2
6	lnc-AL772363.1-1	chr9:140769915-140770132	XLOC_007904
7	lnc-AL772363.1-1	chr9:140771009-140771749	XLOC_007904
8	lnc-AL772363.1-1	chr9:140769915-140770132	XLOC_007904
9	lnc-AL772363.1-1	chr9:140768516-140768684	XLOC_007904
10	lnc-AL772363.1-1	chr9:140762365-140762689	XLOC_007904
11	lnc-AL772363.1-1	chr9:140762379-140762689	ENSG00000203987.2
12	lnc-AL772363.1-1	chr9:140771009-140771749	XLOC_007904
13	lnc-AL772363.1-1	chr9:140768516-140768684	XLOC_007904
14	lnc-AL772363.1-1	chr9:140767616-140767710	XLOC_007904
15	lnc-AL772363.1-1	chr9:140768516-140768666	ENSG00000203987.2
16	lnc-AL772363.1-3	chr9:140843115-140843211	NONHSAT135761
17	lnc-AL772363.1-1	chr9:140762377-140762689	ENSG00000203987.2
18	lnc-AL772363.1-3	chr9:140843618-140844002	NONHSAT135761
19	lnc-AL772363.1-1	chr9:140767517-140767710	XLOC_007904

No data

Variant related genes	Relation type
CACNA1B	TF binding region
ENSG00000203987	TF binding region
CACNA1B	CpG island
ENSG00000203987	CpG island
ENSG00000148399	chromatin interactions
ENSG00000148408	chromatin interactions
ENSG00000206737	chromatin interactions
PRRG1	miRNA target sites
ACIN1	miRNA target sites
GPM6A	miRNA target sites
AKAP11	miRNA target sites

Extended variants
information (count: 5444 )
Associated
traits (count: 19 )

Variant overlapped rSNPs/rCNVs (count:5444 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531747021	chr9:140746233-140746234	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs184607597	chr9:140746241-140746242	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562815139	chr9:140746274-140746275	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531637552	chr9:140746280-140746281	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566990172	chr9:140746288-140746289	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542101429	chr9:140746299-140746300	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78991594	chr9:140746342-140746343	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546254381	chr9:140746344-140746345	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371476436	chr9:140746370-140746371	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78818614	chr9:140746385-140746386	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547493301	chr9:140746442-140746443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538544417	chr9:140746458-140746459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558763508	chr9:140746476-140746477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35018431	chr9:140746547-140746548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570432730	chr9:140746566-140746567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73583348	chr9:140746568-140746569	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs114656280	chr9:140746591-140746592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555115885	chr9:140746592-140746593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76439748	chr9:140746602-140746603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34555141	chr9:140746688-140746689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7390244	chr9:140746691-140746692	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs560277409	chr9:140746692-140746693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187902062	chr9:140746701-140746702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552492734	chr9:140746705-140746706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs148043827	chr9:140746715-140746716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562804505	chr9:140746761-140746762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs116353587	chr9:140746765-140746766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191092881	chr9:140746773-140746774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs71510857	chr9:140746788-140746789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370958087	chr9:140746792-140746793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529183884	chr9:140746803-140746804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111735306	chr9:140746806-140746807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9410060	chr9:140746807-140746808	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs200288798	chr9:140746814-140746815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs7390029	chr9:140746865-140746866	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs566341678	chr9:140746866-140746867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541277846	chr9:140746946-140746947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113676474	chr9:140746957-140746958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568136341	chr9:140746978-140746979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569137528	chr9:140746981-140746982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs116921543	chr9:140746993-140746994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs145982408	chr9:140747017-140747018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369664414	chr9:140747042-140747043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534032111	chr9:140747049-140747050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373212507	chr9:140747074-140747075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112043796	chr9:140747081-140747082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183609889	chr9:140747089-140747090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115764238	chr9:140747118-140747119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116148550	chr9:140747119-140747120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139839735	chr9:140747198-140747199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:19)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	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
Mantle cell lymphoma	19029149	CNVD

Chromatin state (count:782 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140713000-140747200	Weak transcription	Stomach Mucosa	stomach
2	chr9:140745800-140747200	Enhancers	Hela-S3	cervix
3	chr9:140746000-140746600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr9:140746200-140746400	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr9:140746200-140746600	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr9:140750600-140751400	ZNF genes & repeats	Adipose Nuclei	Adipose
7	chr9:140750800-140751000	Bivalent/Poised TSS	Placenta	Placenta
8	chr9:140750800-140751400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:140751400-140761600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr9:140759800-140762400	Enhancers	GM12878-XiMat	blood
11	chr9:140760200-140760400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr9:140760600-140760800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr9:140760600-140760800	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr9:140761600-140761800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:140761800-140767800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:140766800-140767000	Bivalent Enhancer	K562	blood
17	chr9:140767800-140768400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr9:140768400-140768800	Bivalent Enhancer	K562	blood
19	chr9:140768600-140768800	Bivalent Enhancer	Hela-S3	cervix
20	chr9:140770000-140770600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr9:140770400-140770600	Bivalent Enhancer	Brain Germinal Matrix	brain
22	chr9:140770800-140771200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr9:140771200-140771400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr9:140771400-140771600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
25	chr9:140771400-140771600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr9:140771400-140771600	Bivalent Enhancer	Brain Germinal Matrix	brain
27	chr9:140771400-140773000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
28	chr9:140771600-140771800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr9:140771600-140772000	Bivalent Enhancer	Ovary	ovary
30	chr9:140771600-140772200	Enhancers	Fetal Brain Male	brain
31	chr9:140771600-140772200	Active TSS	Fetal Brain Female	brain
32	chr9:140771600-140772800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
33	chr9:140771600-140772800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr9:140771600-140773000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
35	chr9:140771600-140773000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
36	chr9:140771600-140773000	Bivalent Enhancer	Lung	lung
37	chr9:140771600-140773800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
38	chr9:140771600-140773800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
39	chr9:140771600-140773800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
40	chr9:140771800-140772000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
41	chr9:140771800-140772000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
42	chr9:140771800-140772000	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr9:140771800-140772000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr9:140771800-140772000	Bivalent Enhancer	Right Ventricle	heart
45	chr9:140771800-140772200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr9:140771800-140772200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr9:140771800-140772200	Bivalent/Poised TSS	Thymus	Thymus
48	chr9:140771800-140772400	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr9:140771800-140772600	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr9:140771800-140772800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell

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