Variant report

Variant	nsv1025949
Chromosome Location	chr9:44205252-44875930
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2919)
CpG islands
(count:1343)
Chromatin interactive
region (count:1)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2919 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:44875124-44875487	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:44781098-44781371	K562	blood:	n/a	n/a
3	ARID3A	chr9:44799676-44800004	HepG2	liver:	n/a	n/a
4	ATF1	chr9:44781241-44781724	K562	blood:	n/a	n/a
5	BACH1	chr9:44227257-44227630	K562	blood:	n/a	n/a
6	BACH1	chr9:44227184-44227631	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr9:44367161-44367437	GM12878	blood:	n/a	n/a
8	BATF	chr9:44874845-44875096	GM12878	blood:	n/a	n/a
9	BATF	chr9:44306115-44306341	GM12878	blood:	n/a	n/a
10	BATF	chr9:44645234-44645529	GM12878	blood:	n/a	chr9:44645403-44645414
11	BATF	chr9:44556907-44557469	GM12878	blood:	n/a	n/a
12	BATF	chr9:44836556-44836749	GM12878	blood:	n/a	n/a
13	BATF	chr9:44305341-44305592	GM12878	blood:	n/a	n/a
14	BATF	chr9:44306098-44306362	GM12878	blood:	n/a	n/a
15	BATF	chr9:44552199-44552435	GM12878	blood:	n/a	n/a
16	BATF	chr9:44212515-44212942	GM12878	blood:	n/a	chr9:44212712-44212723
17	BATF	chr9:44245375-44245745	GM12878	blood:	n/a	n/a
18	BATF	chr9:44341525-44341789	GM12878	blood:	n/a	chr9:44341638-44341649
19	BATF	chr9:44292256-44292632	GM12878	blood:	n/a	n/a
20	BATF	chr9:44841475-44841709	GM12878	blood:	n/a	n/a
21	BATF	chr9:44342310-44342546	GM12878	blood:	n/a	n/a
22	BATF	chr9:44245873-44246195	GM12878	blood:	n/a	n/a
23	BATF	chr9:44551132-44551329	GM12878	blood:	n/a	n/a
24	BATF	chr9:44402919-44403250	GM12878	blood:	n/a	n/a
25	BATF	chr9:44382132-44382329	GM12878	blood:	n/a	n/a
26	BATF	chr9:44469306-44469638	GM12878	blood:	n/a	n/a
27	BATF	chr9:44401104-44402763	GM12878	blood:	n/a	n/a
28	BATF	chr9:44874916-44875326	GM12878	blood:	n/a	n/a
29	BATF	chr9:44528122-44528281	GM12878	blood:	n/a	n/a
30	BATF	chr9:44556841-44557602	GM12878	blood:	n/a	n/a
31	BATF	chr9:44341546-44341772	GM12878	blood:	n/a	chr9:44341638-44341649
32	BATF	chr9:44539661-44540230	GM12878	blood:	n/a	n/a
33	BATF	chr9:44401329-44401837	GM12878	blood:	n/a	n/a
34	BATF	chr9:44355408-44355626	GM12878	blood:	n/a	n/a
35	BATF	chr9:44403838-44404118	GM12878	blood:	n/a	n/a
36	BATF	chr9:44435839-44436055	GM12878	blood:	n/a	n/a
37	BATF	chr9:44379817-44379994	GM12878	blood:	n/a	chr9:44379913-44379924
38	BATF	chr9:44552225-44552444	GM12878	blood:	n/a	n/a
39	BATF	chr9:44367127-44367454	GM12878	blood:	n/a	n/a
40	BATF	chr9:44355328-44355568	GM12878	blood:	n/a	n/a
41	BATF	chr9:44280534-44280732	GM12878	blood:	n/a	n/a
42	BATF	chr9:44245139-44246113	GM12878	blood:	n/a	n/a
43	BATF	chr9:44539620-44540220	GM12878	blood:	n/a	n/a
44	BATF	chr9:44606159-44606345	GM12878	blood:	n/a	n/a
45	BATF	chr9:44434645-44435048	GM12878	blood:	n/a	n/a
46	BATF	chr9:44742136-44742432	GM12878	blood:	n/a	n/a
47	BATF	chr9:44402875-44403302	GM12878	blood:	n/a	n/a
48	BATF	chr9:44342315-44342531	GM12878	blood:	n/a	n/a
49	BATF	chr9:44265544-44265770	GM12878	blood:	n/a	n/a
50	BATF	chr9:44577860-44578259	GM12878	blood:	n/a	chr9:44577967-44577975

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:44745070-44745120	HCT-116	colon:	n/a
2	chr9:44745070-44745120	HCT-116	colon:	n/a
3	chr9:44866782-44866832	AG10803	skin:	n/a
4	chr9:44401998-44402048	NHDF-neo	bronchial:	n/a
5	chr9:44866782-44866832	Jurkat	blood:	n/a
6	chr9:44422602-44422652	RPTEC	kidney:	n/a
7	chr9:44227339-44227389	PANC-1	pancreas:	n/a
8	chr9:44227339-44227389	U87	brain:	n/a
9	chr9:44874632-44874682	HEEpiC	esophagus:	n/a
10	chr9:44857677-44857727	HCF	heart:	n/a
11	chr9:44745070-44745120	NHBE	bronchial:	n/a
12	chr9:44866782-44866832	CMK	blood:	n/a
13	chr9:44744257-44744307	HRE	kidney:	n/a
14	chr9:44745070-44745120	Caco-2	colon:	n/a
15	chr9:44873530-44873580	HCF	heart:	n/a
16	chr9:44742086-44742136	MCF-7	breast:	n/a
17	chr9:44401998-44402048	PFSK-1	brain:	n/a
18	chr9:44868911-44868961	AG09319	gingival:	n/a
19	chr9:44422602-44422652	H1-hESC	embryonic stem cell:	embryo
20	chr9:44745070-44745120	SK-N-SH_RA	brain:	n/a
21	chr9:44867546-44867596	GM19239	blood:	n/a
22	chr9:44868911-44868961	PrEC	prostate:	n/a
23	chr9:44227210-44227260	Hela-S3	cervix:	n/a
24	chr9:44313114-44313164	SK-N-SH_RA	brain:	n/a
25	chr9:44866782-44866832	GM12892	blood:	n/a
26	chr9:44227210-44227260	HUVEC	blood vessel:	n/a
27	chr9:44874873-44874923	GM12878	blood:	n/a
28	chr9:44859075-44859125	HepG2	liver:	n/a
29	chr9:44874632-44874682	HNPCEpiC	eye:	n/a
30	chr9:44227339-44227389	NHBE	bronchial:	n/a
31	chr9:44313114-44313164	Caco-2	colon:	n/a
32	chr9:44868911-44868961	AG10803	skin:	n/a
33	chr9:44867546-44867596	SK-N-SH_RA	brain:	n/a
34	chr9:44742086-44742136	PANC-1	pancreas:	n/a
35	chr9:44873530-44873580	ProgFib	skin:	n/a
36	chr9:44313114-44313164	NT2-D1	testis:	n/a
37	chr9:44873530-44873580	AG10803	skin:	n/a
38	chr9:44873530-44873580	H1-hESC	embryonic stem cell:	embryo
39	chr9:44227339-44227389	K562	blood:	n/a
40	chr9:44873816-44873866	HCF	heart:	n/a
41	chr9:44841495-44841545	H1-hESC	embryonic stem cell:	embryo
42	chr9:44874873-44874923	Hepatocyte	liver:	n/a
43	chr9:44874873-44874923	BJ	skin:	n/a
44	chr9:44313114-44313164	SK-N-SH	brain:	n/a
45	chr9:44401998-44402048	HAEpiC	amniotic membrane:	n/a
46	chr9:44841495-44841545	PFSK-1	brain:	n/a
47	chr9:44841495-44841545	AG04449	skin:	fetal
48	chr9:44859075-44859125	SAEC	small airway:	n/a
49	chr9:44420179-44420229	HAEpiC	amniotic membrane:	n/a
50	chr9:44873530-44873580	Hepatocyte	liver:	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:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM75A6-14	chr9:44674678-44674747	NONHSAT131392
2	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424
3	lnc-CNTNAP3B-1	chr9:44387768-44387853	ENSG00000229311
4	lnc-RP11-160N1.10.1-4	chr9:44763709-44763841	NONHSAT131393
5	lnc-FAM75A6-3	chr9:44256189-44256817	ENSG00000233424
6	lnc-RP11-160N1.10.1-1	chr9:44828088-44828239	ENSG00000231248.2
7	lnc-RP11-160N1.10.1-3	chr9:44874008-44874226	NONHSAT131397
8	lnc-FAM75A6-14	chr9:44672800-44672959	NONHSAT131392
9	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424
10	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424.2
11	lnc-FAM75A6-14	chr9:44676388-44676450	NONHSAT131392
12	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424.2
13	lnc-CNTNAP3B-1	chr9:44387768-44387853	NR_046203
14	lnc-RP11-160N1.10.1-2	chr9:44403060-44403260	ENSG00000237357
15	lnc-RP11-160N1.10.1-1	chr9:44823714-44823845	ENSG00000231248.2
16	lnc-RP11-160N1.10.1-5	chr9:44562093-44562588	NONHSAT131391
17	lnc-RP11-160N1.10.1-4	chr9:44775383-44775517	NONHSAT131393
18	lnc-RP11-160N1.10.1-2	chr9:44402460-44402515	ENSG00000237357
19	lnc-RP11-160N1.10.1-4	chr9:44768084-44768235	NONHSAT131393
20	lnc-CNTNAP3B-1	chr9:44391077-44391705	ENSG00000229311
21	lnc-FAM75A6-13	chr9:44477549-44477882	NONHSAT131390
22	lnc-RP11-160N1.10.1-3	chr9:44873417-44873492	NONHSAT131396
23	lnc-CNTNAP3B-1	chr9:44391077-44391416	NR_046203
24	lnc-RP11-160N1.10.1-1	chr9:44835387-44835521	ENSG00000231248.2
25	lnc-FAM75A6-14	chr9:44673720-44673889	NONHSAT131392
26	lnc-RP11-160N1.10.1-3	chr9:44874017-44874224	NONHSAT131396
27	lnc-CNTNAP3B-1	chr9:44384585-44387483	ENSG00000229311
28	lnc-RP11-160N1.10.1-1	chr9:44834508-44834806	ENSG00000231248.2
29	lnc-CNTNAP3B-1	chr9:44387387-44387483	NR_046203
30	lnc-RP11-160N1.10.1-4	chr9:44774504-44774802	NONHSAT131393
31	lnc-FAM75A6-3	chr9:44256580-44256817	ENSG00000233424.2
32	lnc-FAM75A6-13	chr9:44478194-44478456	NONHSAT131390

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
ENSG00000231454	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
ENSG00000204814	TF binding region
ENSG00000268234	TF binding region
ENSG00000223664	CpG island
ATP5A1P6	CpG island
ENSG00000231248	CpG island
ENSG00000228920	CpG island
ENSG00000230245	CpG island
ENSG00000231454	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
ENSG00000204814	CpG island
ENSG00000268234	CpG island

Extended variants
information (count: 2830 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2830 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200775245	chr9:44213649-44213650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185310249	chr9:44213655-44213656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145167070	chr9:44213689-44213690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138504846	chr9:44213696-44213697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs28578180	chr9:44213698-44213699	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs568032184	chr9:44213702-44213703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs526932	chr9:44213717-44213718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577144302	chr9:44213739-44213740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541103523	chr9:44213770-44213771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559879353	chr9:44213788-44213789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530266245	chr9:44213800-44213801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542798678	chr9:44213820-44213821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561073397	chr9:44213865-44213866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537162494	chr9:44213866-44213867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550070750	chr9:44213885-44213886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571480657	chr9:44213901-44213902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs28705255	chr9:44213923-44213924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547123308	chr9:44213938-44213939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565388725	chr9:44213942-44213943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535950495	chr9:44213967-44213968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs28501649	chr9:44213995-44213996	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs569934843	chr9:44214016-44214017	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs537271613	chr9:44214026-44214027	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs570624431	chr9:44214030-44214031	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs559184883	chr9:44214167-44214168	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs577509791	chr9:44214174-44214175	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs539278646	chr9:44214202-44214203	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs552834336	chr9:44214206-44214207	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs541415384	chr9:44214208-44214209	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs553407973	chr9:44214213-44214214	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs574948830	chr9:44214214-44214215	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs542360400	chr9:44214224-44214225	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs142853025	chr9:44214233-44214234	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs531512420	chr9:44214244-44214245	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs183201745	chr9:44214271-44214272	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs187173979	chr9:44214278-44214279	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs532308527	chr9:44214280-44214281	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs547327181	chr9:44214322-44214323	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs28431036	chr9:44214325-44214326	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs202036141	chr9:44214333-44214334	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs192280171	chr9:44214337-44214338	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs547857062	chr9:44214348-44214349	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs555736782	chr9:44214350-44214351	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs140685213	chr9:44214371-44214372	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs558934387	chr9:44214382-44214383	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs182985999	chr9:44214399-44214400	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs565034292	chr9:44227033-44227034	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs150209686	chr9:44227059-44227060	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs111868578	chr9:44227098-44227099	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs71496188	chr9:44227109-44227110	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:309 , 50 per page) page: 1 2 3 4 5 6 7

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

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