Variant report

Variant	nsv1032349
Chromosome Location	chr9:44192208-44855725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2640)
CpG islands
(count:732)
Chromatin interactive
region (count:1)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2640 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:44799676-44800004	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:44781098-44781371	K562	blood:	n/a	n/a
3	ATF1	chr9:44781241-44781724	K562	blood:	n/a	n/a
4	BACH1	chr9:44227184-44227631	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:44227257-44227630	K562	blood:	n/a	n/a
6	BATF	chr9:44402875-44403302	GM12878	blood:	n/a	n/a
7	BATF	chr9:44605070-44605809	GM12878	blood:	n/a	n/a
8	BATF	chr9:44606159-44606345	GM12878	blood:	n/a	n/a
9	BATF	chr9:44265544-44265770	GM12878	blood:	n/a	n/a
10	BATF	chr9:44645234-44645529	GM12878	blood:	n/a	chr9:44645403-44645414
11	BATF	chr9:44645280-44645491	GM12878	blood:	n/a	chr9:44645403-44645414
12	BATF	chr9:44577809-44578267	GM12878	blood:	n/a	chr9:44577967-44577975
13	BATF	chr9:44528122-44528281	GM12878	blood:	n/a	n/a
14	BATF	chr9:44306098-44306362	GM12878	blood:	n/a	n/a
15	BATF	chr9:44212521-44212907	GM12878	blood:	n/a	chr9:44212712-44212723
16	BATF	chr9:44292314-44292554	GM12878	blood:	n/a	n/a
17	BATF	chr9:44212515-44212942	GM12878	blood:	n/a	chr9:44212712-44212723
18	BATF	chr9:44556841-44557602	GM12878	blood:	n/a	n/a
19	BATF	chr9:44836556-44836749	GM12878	blood:	n/a	n/a
20	BATF	chr9:44434613-44435054	GM12878	blood:	n/a	n/a
21	BATF	chr9:44551132-44551329	GM12878	blood:	n/a	n/a
22	BATF	chr9:44401329-44401837	GM12878	blood:	n/a	n/a
23	BATF	chr9:44552199-44552435	GM12878	blood:	n/a	n/a
24	BATF	chr9:44419769-44419966	GM12878	blood:	n/a	n/a
25	BATF	chr9:44552225-44552444	GM12878	blood:	n/a	n/a
26	BATF	chr9:44367161-44367437	GM12878	blood:	n/a	n/a
27	BATF	chr9:44305341-44305592	GM12878	blood:	n/a	n/a
28	BATF	chr9:44539620-44540220	GM12878	blood:	n/a	n/a
29	BATF	chr9:44280452-44280759	GM12878	blood:	n/a	n/a
30	BATF	chr9:44533431-44533653	GM12878	blood:	n/a	n/a
31	BATF	chr9:44742136-44742432	GM12878	blood:	n/a	n/a
32	BATF	chr9:44245375-44245745	GM12878	blood:	n/a	n/a
33	BATF	chr9:44306115-44306341	GM12878	blood:	n/a	n/a
34	BATF	chr9:44355408-44355626	GM12878	blood:	n/a	n/a
35	BATF	chr9:44382132-44382329	GM12878	blood:	n/a	n/a
36	BATF	chr9:44245139-44246113	GM12878	blood:	n/a	n/a
37	BATF	chr9:44434645-44435048	GM12878	blood:	n/a	n/a
38	BATF	chr9:44403838-44404118	GM12878	blood:	n/a	n/a
39	BATF	chr9:44577860-44578259	GM12878	blood:	n/a	chr9:44577967-44577975
40	BATF	chr9:44280534-44280732	GM12878	blood:	n/a	n/a
41	BATF	chr9:44355328-44355568	GM12878	blood:	n/a	n/a
42	BATF	chr9:44292256-44292632	GM12878	blood:	n/a	n/a
43	BATF	chr9:44341546-44341772	GM12878	blood:	n/a	chr9:44341638-44341649
44	BATF	chr9:44841475-44841709	GM12878	blood:	n/a	n/a
45	BATF	chr9:44341525-44341789	GM12878	blood:	n/a	chr9:44341638-44341649
46	BATF	chr9:44605098-44605838	GM12878	blood:	n/a	n/a
47	BATF	chr9:44550459-44550750	GM12878	blood:	n/a	n/a
48	BATF	chr9:44435839-44436055	GM12878	blood:	n/a	n/a
49	BATF	chr9:44306841-44307126	GM12878	blood:	n/a	n/a
50	BATF	chr9:44402919-44403250	GM12878	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:44744257-44744307	HEEpiC	esophagus:	n/a
2	chr9:44742086-44742136	GM12892	blood:	n/a
3	chr9:44422602-44422652	AG09309	skin:	n/a
4	chr9:44744257-44744307	AG04449	skin:	fetal
5	chr9:44401998-44402048	NT2-D1	testis:	n/a
6	chr9:44422602-44422652	ProgFib	skin:	n/a
7	chr9:44744257-44744307	Jurkat	blood:	n/a
8	chr9:44422602-44422652	HRPEpiC	eye:	n/a
9	chr9:44743856-44743906	GM19239	blood:	n/a
10	chr9:44743856-44743906	AoSMC	blood vessel:	n/a
11	chr9:44227210-44227260	BJ	skin:	n/a
12	chr9:44742086-44742136	NT2-D1	testis:	n/a
13	chr9:44227210-44227260	K562	blood:	n/a
14	chr9:44744257-44744307	LNCaP	prostate:	n/a
15	chr9:44842398-44842448	A549	lung:	n/a
16	chr9:44401998-44402048	T-47D	breast:	n/a
17	chr9:44744257-44744307	RPTEC	kidney:	n/a
18	chr9:44744257-44744307	HIPEpiC	eye:	n/a
19	chr9:44841495-44841545	NH-A	brain:	n/a
20	chr9:44745070-44745120	HepG2	liver:	n/a
21	chr9:44742086-44742136	BJ	skin:	n/a
22	chr9:44422602-44422652	SK-N-SH	brain:	n/a
23	chr9:44401998-44402048	PANC-1	pancreas:	n/a
24	chr9:44420179-44420229	HRPEpiC	eye:	n/a
25	chr9:44742086-44742136	HUVEC	blood vessel:	n/a
26	chr9:44227210-44227260	AG09319	gingival:	n/a
27	chr9:44227210-44227260	NH-A	brain:	n/a
28	chr9:44841495-44841545	NHDF-neo	bronchial:	n/a
29	chr9:44422602-44422652	HMEC	breast:	n/a
30	chr9:44422602-44422652	ovcar-3	ovarian:	n/a
31	chr9:44401998-44402048	CMK	blood:	n/a
32	chr9:44842398-44842448	AG10803	skin:	n/a
33	chr9:44227210-44227260	AG04450	lung:	fetal
34	chr9:44227339-44227389	T-47D	breast:	n/a
35	chr9:44420179-44420229	SK-N-SH_RA	brain:	n/a
36	chr9:44745070-44745120	ECC-1	luminal epithelium:	n/a
37	chr9:44742086-44742136	HIPEpiC	eye:	n/a
38	chr9:44401998-44402048	ECC-1	luminal epithelium:	n/a
39	chr9:44745070-44745120	ovcar-3	ovarian:	n/a
40	chr9:44313114-44313164	SK-N-SH	brain:	n/a
41	chr9:44743856-44743906	SK-N-SH	brain:	n/a
42	chr9:44227339-44227389	NHDF-neo	bronchial:	n/a
43	chr9:44742086-44742136	PrEC	prostate:	n/a
44	chr9:44422602-44422652	NB4	blood:	n/a
45	chr9:44744257-44744307	HRCEpiC	kidney:	n/a
46	chr9:44743856-44743906	MCF-7	breast:	n/a
47	chr9:44227339-44227389	HCM	heart:	n/a
48	chr9:44313114-44313164	HUVEC	blood vessel:	n/a
49	chr9:44420179-44420229	HUVEC	blood vessel:	n/a
50	chr9:44227339-44227389	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:107699957..107700478-chr9:44227430..44227950,2	MCF-7	breast:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM75A6-14	chr9:44672800-44672959	NONHSAT131392
2	lnc-CNTNAP3B-1	chr9:44387768-44387853	ENSG00000229311
3	lnc-FAM75A6-13	chr9:44477549-44477882	NONHSAT131390
4	lnc-FAM75A6-14	chr9:44673720-44673889	NONHSAT131392
5	lnc-RP11-160N1.10.1-4	chr9:44774504-44774802	NONHSAT131393
6	lnc-CNTNAP3B-1	chr9:44384585-44387483	ENSG00000229311
7	lnc-RP11-160N1.10.1-1	chr9:44834508-44834806	ENSG00000231248.2
8	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424
9	lnc-FAM75A6-14	chr9:44676388-44676450	NONHSAT131392
10	lnc-CNTNAP3B-1	chr9:44391077-44391416	NR_046203
11	lnc-CNTNAP3B-1	chr9:44391077-44391705	ENSG00000229311
12	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424.2
13	lnc-RP11-160N1.10.1-1	chr9:44835387-44835521	ENSG00000231248.2
14	lnc-RP11-160N1.10.1-2	chr9:44402460-44402515	ENSG00000237357
15	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424
16	lnc-RP11-160N1.10.1-2	chr9:44403060-44403260	ENSG00000237357
17	lnc-RP11-160N1.10.1-4	chr9:44775383-44775517	NONHSAT131393
18	lnc-CNTNAP3B-1	chr9:44387768-44387853	NR_046203
19	lnc-RP11-160N1.10.1-4	chr9:44768084-44768235	NONHSAT131393
20	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424.2
21	lnc-CNTNAP3B-1	chr9:44387387-44387483	NR_046203
22	lnc-RP11-160N1.10.1-1	chr9:44823714-44823845	ENSG00000231248.2
23	lnc-FAM75A6-3	chr9:44256189-44256817	ENSG00000233424
24	lnc-RP11-160N1.10.1-4	chr9:44763709-44763841	NONHSAT131393
25	lnc-FAM75A6-14	chr9:44674678-44674747	NONHSAT131392
26	lnc-FAM75A6-3	chr9:44256580-44256817	ENSG00000233424.2
27	lnc-RP11-160N1.10.1-1	chr9:44828088-44828239	ENSG00000231248.2
28	lnc-FAM75A6-13	chr9:44478194-44478456	NONHSAT131390
29	lnc-RP11-160N1.10.1-5	chr9:44562093-44562588	NONHSAT131391

No data

Variant related genes	Relation type
ENSG00000223664	TF binding region
ATP5A1P6	TF binding region
ENSG00000231248	TF binding region
ENSG00000228920	TF binding region
ENSG00000230245	TF binding region
ENSG00000227353	TF binding region
ENSG00000216829	TF binding region
ENSG00000268708	TF binding region
ENSG00000212952	TF binding region
ENSG00000238933	TF binding region
ENSG00000237357	TF binding region
RBPJP6	TF binding region
ENSG00000204816	TF binding region
ENSG00000233424	TF binding region
ENSG00000229311	TF binding region
ENSG00000268234	TF binding region
ENSG00000223664	CpG island
ATP5A1P6	CpG island
ENSG00000231248	CpG island
ENSG00000228920	CpG island
ENSG00000230245	CpG island
ENSG00000227353	CpG island
ENSG00000216829	CpG island
ENSG00000268708	CpG island
ENSG00000212952	CpG island
ENSG00000238933	CpG island
ENSG00000237357	CpG island
RBPJP6	CpG island
ENSG00000204816	CpG island
ENSG00000233424	CpG island
ENSG00000229311	CpG island
ENSG00000268234	CpG island

Extended variants
information (count: 1942 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1942 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532398158	chr9:44195207-44195208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs145481633	chr9:44195214-44195215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115336600	chr9:44195215-44195216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs28522906	chr9:44195234-44195235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs28481845	chr9:44195263-44195264	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs186668203	chr9:44195274-44195275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560407348	chr9:44195276-44195277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191119372	chr9:44195313-44195314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546464759	chr9:44195315-44195316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146949790	chr9:44195319-44195320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529149463	chr9:44195320-44195321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550465033	chr9:44195325-44195326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs28634584	chr9:44195350-44195351	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs28586892	chr9:44195357-44195358	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs28453702	chr9:44195373-44195374	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs566421681	chr9:44195425-44195426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142151869	chr9:44195445-44195446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538299051	chr9:44195465-44195466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs374079517	chr9:44195467-44195468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368330429	chr9:44195475-44195476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146013146	chr9:44195491-44195492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148271628	chr9:44195494-44195495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570960217	chr9:44195512-44195513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184932534	chr9:44195516-44195517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548398620	chr9:44195521-44195522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188249511	chr9:44195535-44195536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141382502	chr9:44195559-44195560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192957493	chr9:44195564-44195565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150799815	chr9:44195594-44195595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77106521	chr9:44195661-44195662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79537803	chr9:44195662-44195663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1944221	chr9:44195681-44195682	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs561500524	chr9:44195695-44195696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529064658	chr9:44195708-44195709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550427458	chr9:44195714-44195715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562464314	chr9:44195721-44195722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141980965	chr9:44195728-44195729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs146323503	chr9:44195731-44195732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185211303	chr9:44195736-44195737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533646728	chr9:44195746-44195747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549100974	chr9:44195748-44195749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs28393023	chr9:44195755-44195756	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs534580965	chr9:44195786-44195787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554628769	chr9:44195791-44195792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538465351	chr9:44195792-44195793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188924466	chr9:44195802-44195803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139644824	chr9:44195812-44195813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539361468	chr9:44195826-44195827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553877649	chr9:44195829-44195830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs28431771	chr9:44195831-44195832	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:70)

Disease	PMID	Source
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
Oral squamous cell carcinoma	17134496	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Lung adenocarcinoma	17086460	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	17086460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Schizophrenia	20967226	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:44195200-44196000	Enhancers	Adipose Nuclei	Adipose
2	chr9:44213600-44214200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr9:44214000-44214400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr9:44214000-44214400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
5	chr9:44227000-44227200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr9:44227000-44227200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr9:44227000-44227200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr9:44227000-44227200	Enhancers	Adipose Nuclei	Adipose
9	chr9:44227000-44227200	Enhancers	Stomach Smooth Muscle	stomach
10	chr9:44227000-44227200	Enhancers	NHEK	skin
11	chr9:44227000-44227600	Active TSS	A549	lung
12	chr9:44227200-44227400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
13	chr9:44227200-44227400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr9:44227200-44227400	Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr9:44227200-44227400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr9:44227200-44227400	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
17	chr9:44227200-44227400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr9:44227200-44227400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr9:44227200-44227400	Active TSS	Brain Cingulate Gyrus	brain
20	chr9:44227200-44227400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr9:44227200-44227400	Active TSS	Duodenum Smooth Muscle	Duodenum
22	chr9:44227200-44227400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
23	chr9:44227200-44227400	Active TSS	Pancreas	Pancrea
24	chr9:44227200-44227400	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr9:44227200-44227600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
26	chr9:44227200-44227600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr9:44227200-44227600	Active TSS	H9 Cell Line	embryonic stem cell
28	chr9:44227200-44227600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr9:44227200-44227600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr9:44227200-44227600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr9:44227200-44227600	Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr9:44227200-44227600	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
33	chr9:44227200-44227600	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr9:44227200-44227600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr9:44227200-44227600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr9:44227200-44227600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr9:44227200-44227600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr9:44227200-44227600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr9:44227200-44227600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr9:44227200-44227600	Active TSS	Brain Germinal Matrix	brain
41	chr9:44227200-44227600	Active TSS	Esophagus	oesophagus
42	chr9:44227200-44227600	Active TSS	Stomach Mucosa	stomach
43	chr9:44227200-44227600	Flanking Active TSS	Stomach Smooth Muscle	stomach
44	chr9:44227200-44227600	Enhancers	HMEC	breast
45	chr9:44227200-44227800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr9:44227200-44227800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
47	chr9:44227200-44227800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
48	chr9:44227200-44227800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr9:44227200-44227800	Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr9:44227200-44227800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell

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