Variant report

Variant	nsv540000
Chromosome Location	chr9:10972764-11530615
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:11064894-11065285	K562	blood:	n/a	n/a
2	ARID3A	chr9:11064055-11064488	K562	blood:	n/a	n/a
3	ATF1	chr9:11064943-11065293	K562	blood:	n/a	n/a
4	BACH1	chr9:11067007-11067064	K562	blood:	n/a	n/a
5	BACH1	chr9:11016111-11016284	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr9:11038049-11038208	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr9:11064885-11065303	K562	blood:	n/a	n/a
8	BHLHE40	chr9:11064998-11065193	HepG2	liver:	n/a	n/a
9	BHLHE40	chr9:11338205-11338405	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:11065067-11065094	GM12878	blood:	n/a	n/a
11	BRCA1	chr9:11064953-11065285	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr9:11319527-11319802	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr9:11064529-11064729	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr9:11272473-11272479	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr9:11064870-11065315	K562	blood:	n/a	n/a
16	CBX3	chr9:11269115-11269340	K562	blood:	n/a	n/a
17	CEBPB	chr9:11422396-11422505	HepG2	liver:	n/a	n/a
18	CEBPB	chr9:11356165-11356517	ECC-1	luminal epithelium:	n/a	chr9:11356437-11356448
19	CEBPB	chr9:11457818-11458170	HepG2	liver:	n/a	chr9:11457991-11458008 chr9:11457994-11458007 chr9:11457994-11458005
20	CEBPB	chr9:11217166-11217491	IMR90	lung:	n/a	n/a
21	CEBPB	chr9:11457829-11458659	H1-hESC	embryonic stem cell:	n/a	chr9:11457991-11458008 chr9:11457994-11458007 chr9:11458637-11458645 chr9:11457994-11458005
22	CEBPB	chr9:11084639-11084926	A549	lung:	n/a	chr9:11084785-11084796 chr9:11084784-11084797 chr9:11084784-11084795
23	CEBPB	chr9:11257560-11257807	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:11258112-11258370	A549	lung:	n/a	chr9:11258233-11258244
25	CEBPB	chr9:11022120-11022420	Hela-S3	cervix:	n/a	chr9:11022289-11022300
26	CEBPB	chr9:11457881-11458153	K562	blood:	n/a	chr9:11457991-11458008 chr9:11457994-11458007 chr9:11457994-11458005
27	CEBPB	chr9:11357845-11358150	IMR90	lung:	n/a	chr9:11357994-11358007 chr9:11357994-11358005 chr9:11357937-11357948
28	CEBPB	chr9:10978428-10978694	HepG2	liver:	n/a	chr9:10978574-10978585
29	CEBPB	chr9:11208917-11208996	A549	lung:	n/a	chr9:11208951-11208964
30	CEBPB	chr9:11372456-11372755	HepG2	liver:	n/a	chr9:11372602-11372613
31	CEBPB	chr9:11143390-11143713	IMR90	lung:	n/a	chr9:11143522-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143523-11143534 chr9:11143524-11143533
32	CEBPB	chr9:11334920-11335231	HepG2	liver:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
33	CEBPB	chr9:11258112-11258312	K562	blood:	n/a	chr9:11258233-11258244
34	CEBPB	chr9:11334898-11335195	A549	lung:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
35	CEBPB	chr9:11407921-11408170	HepG2	liver:	n/a	chr9:11408023-11408034 chr9:11408023-11408036
36	CEBPB	chr9:11143432-11143632	H1-hESC	embryonic stem cell:	n/a	chr9:11143522-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143523-11143534 chr9:11143524-11143533
37	CEBPB	chr9:11340773-11341042	HepG2	liver:	n/a	chr9:11340918-11340929
38	CEBPB	chr9:11049857-11050082	K562	blood:	n/a	n/a
39	CEBPB	chr9:11221528-11221540	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr9:11084605-11084942	HepG2	liver:	n/a	chr9:11084785-11084796 chr9:11084784-11084797 chr9:11084784-11084795
41	CEBPB	chr9:11407906-11408170	A549	lung:	n/a	chr9:11408023-11408034 chr9:11408023-11408036
42	CEBPB	chr9:11143392-11143656	K562	blood:	n/a	chr9:11143522-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143523-11143534 chr9:11143524-11143533
43	CEBPB	chr9:11334982-11335237	Hela-S3	cervix:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
44	CEBPB	chr9:10997740-10997983	HepG2	liver:	n/a	chr9:10997888-10997899
45	CEBPB	chr9:11349131-11349344	H1-hESC	embryonic stem cell:	n/a	chr9:11349299-11349310
46	CEBPB	chr9:11221350-11221590	IMR90	lung:	n/a	n/a
47	CEBPB	chr9:11335919-11336119	HepG2	liver:	n/a	n/a
48	CEBPB	chr9:11022148-11022435	IMR90	lung:	n/a	chr9:11022289-11022300
49	CEBPB	chr9:11073733-11074087	HepG2	liver:	n/a	chr9:11073895-11073908 chr9:11073895-11073906
50	CEBPB	chr9:11372474-11372712	A549	lung:	n/a	chr9:11372602-11372613

No.	Distal block	Cell Line	Cell type
1	chr9:11115862..11118704-chr9:11119627..11122004,2	MCF-7	breast:
2	chr11:13082457..13083259-chr9:11319197..11319700,2	MCF-7	breast:
3	chr17:41381793..41383489-chr9:11453391..11454891,3	K562	blood:
4	chr9:11056337..11059587-chr9:11061284..11064646,4	K562	blood:
5	chr9:11044597..11046205-chr9:11057945..11060223,2	MCF-7	breast:
6	chr9:11216192..11218001-chr9:11219669..11221559,2	K562	blood:
7	chr9:11047082..11049411-chr9:11061377..11064321,2	K562	blood:
8	chr9:11039996..11042346-chr9:11065271..11066776,2	K562	blood:
9	chr9:11052013..11055648-chr9:11062078..11065783,4	K562	blood:
10	chr9:11018319..11020122-chr9:11028284..11030426,2	K562	blood:
11	chr9:11018319..11020122-chr9:11028284..11030426,2	K562	blood:
12	chr9:11026162..11028762-chr9:11041183..11043715,2	K562	blood:
13	chr9:11064416..11066663-chr9:11091382..11093294,2	MCF-7	breast:
14	chr16:12541131..12541857-chr9:11173536..11174397,2	MCF-7	breast:
15	chr9:11056159..11057837-chr9:11062194..11064646,2	K562	blood:
16	chr9:11044597..11046205-chr9:11057945..11060223,2	MCF-7	breast:
17	chr9:11056337..11059587-chr9:11061284..11064646,4	K562	blood:
18	chr1:210502189..210502757-chr9:11220602..11221102,2	HCT-116	colon:
19	chr9:10855837..10856356-chr9:11319207..11319905,2	MCF-7	breast:
20	chr9:11053156..11054741-chr9:11055812..11058059,2	K562	blood:
21	chr9:11064416..11066663-chr9:11091382..11093294,2	MCF-7	breast:
22	chr9:11216192..11218001-chr9:11219669..11221559,2	K562	blood:
23	chr9:11063987..11066726-chr9:11070793..11073075,2	MCF-7	breast:
24	chr9:10855589..10857004-chr9:11319142..11320476,6	MCF-7	breast:
25	chr9:11056159..11057837-chr9:11062194..11064646,2	K562	blood:
26	chr9:11053156..11054741-chr9:11055812..11058059,2	K562	blood:
27	chr9:11026162..11028762-chr9:11041183..11043715,2	K562	blood:
28	chr9:10366359..10367238-chr9:11319480..11320059,2	MCF-7	breast:
29	chr9:11049044..11051208-chr9:11053146..11055450,2	K562	blood:
30	chr11:62609117..62610638-chr9:11453391..11454911,2	K562	blood:
31	chr9:11051115..11054715-chr9:11062496..11065504,4	K562	blood:
32	chr9:11052013..11055648-chr9:11062078..11065783,4	K562	blood:
33	chr9:11047082..11049411-chr9:11061377..11064321,2	K562	blood:
34	chr9:11059291..11061789-chr9:11063668..11065240,2	MCF-7	breast:
35	chr9:11059291..11061789-chr9:11063668..11065240,2	MCF-7	breast:
36	chr9:11115862..11118704-chr9:11119627..11122004,2	MCF-7	breast:
37	chr9:11051115..11054715-chr9:11062496..11065504,4	K562	blood:
38	chr9:11047509..11049109-chr9:11061184..11063575,2	MCF-7	breast:
39	chr9:11063987..11066726-chr9:11070793..11073075,2	MCF-7	breast:
40	chr9:11047509..11049109-chr9:11061184..11063575,2	MCF-7	breast:
41	chr9:11039996..11042346-chr9:11065271..11066776,2	K562	blood:
42	chr9:11049044..11051208-chr9:11053146..11055450,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRD-4	chr9:11275314-11275536	XLOC_007646
2	lnc-PTPRD-2	chr9:11097567-11097597	XLOC_007644
3	lnc-PTPRD-3	chr9:11172260-11172372	XLOC_007645
4	lnc-TYRP1-2	chr9:11277589-11277655	XLOC_007281
5	lnc-PTPRD-9	chr9:11266253-11266314	NONHSAT130211
6	lnc-PTPRD-3	chr9:11159533-11159565	XLOC_007645
7	lnc-TYRP1-1	chr9:11313363-11313595	XLOC_007282
8	lnc-PTPRD-9	chr9:11265314-11265536	NONHSAT130211
9	lnc-TYRP1-1	chr9:11325743-11325750	XLOC_007282
10	lnc-PTPRD-3	chr9:11194276-11194381	XLOC_007645
11	lnc-PTPRD-2	chr9:11108072-11109984	XLOC_007644
12	lnc-PTPRD-3	chr9:11143876-11144029	XLOC_007645
13	lnc-TYRP1-2	chr9:11277792-11277964	XLOC_007281
14	lnc-PTPRD-4	chr9:11276253-11276314	XLOC_007646

Variant related genes	Relation type
ENSG00000230365	TF binding region
ENSG00000234146	TF binding region
ENSG00000054392	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000133316	chromatin interactions
CSRNP3	miRNA target sites
CSNK1G2	miRNA target sites

Extended variants
information (count: 9426 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:9426 , 50 per page) page: 1 2 3 4 5 6 7 ... 189

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545716594	chr9:10999628-10999629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs556386570	chr9:10999646-10999647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72706899	chr9:10999687-10999688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs61655690	chr9:10999750-10999751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145607009	chr9:10999758-10999759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567755545	chr9:10999767-10999768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561353420	chr9:10999778-10999779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs527327069	chr9:10999800-10999801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575816601	chr9:10999809-10999810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540723921	chr9:10999838-10999839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182324159	chr9:10999839-10999840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544443120	chr9:10999892-10999893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs55709020	chr9:10999899-10999900	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs547732234	chr9:10999913-10999914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10959445	chr9:10999923-10999924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147714064	chr9:10999932-10999933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377133055	chr9:10999941-10999942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186633761	chr9:10999944-10999945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549741270	chr9:10999981-10999982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566079234	chr9:10999989-10999990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540323615	chr9:11000004-11000005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535048923	chr9:11000046-11000047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551839933	chr9:11000059-11000060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571664221	chr9:11000067-11000068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560201612	chr9:11000121-11000122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201723230	chr9:11000219-11000220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532101464	chr9:11000227-11000228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192755401	chr9:11000232-11000233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79513978	chr9:11000315-11000316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556084661	chr9:11000392-11000393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370553039	chr9:11000411-11000412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140437110	chr9:11000416-11000417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144271132	chr9:11000434-11000435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs151148839	chr9:11000440-11000441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs117572986	chr9:11000499-11000500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184757781	chr9:11000502-11000503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564180890	chr9:11000506-11000507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140043807	chr9:11000514-11000515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543955396	chr9:11000539-11000540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563722658	chr9:11000561-11000562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1330250	chr9:11000575-11000576	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs190085890	chr9:11000594-11000595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs60460877	chr9:11000607-11000608	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs528462879	chr9:11000672-11000673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557935282	chr9:11000674-11000675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141841766	chr9:11000693-11000694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368361726	chr9:11000695-11000696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551504763	chr9:11000696-11000697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571666776	chr9:11000697-11000698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537155936	chr9:11000704-11000705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
abnormal development	18461090	CNVD
Disorders of sex development	21048976	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
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21080181	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
Melanoma	18172304	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
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164920	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Melanoma	22183965	CNVD
Barrett''s syndrome	19417022	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Melanoma	20688739	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD

Chromatin state (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:10999600-11000000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:10999600-11000000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr9:11000000-11002600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:11016200-11016600	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr9:11016200-11016800	Enhancers	Placenta Amnion	Placenta Amnion
6	chr9:11016400-11016800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:11016600-11017000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr9:11021800-11023000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr9:11023400-11023600	Enhancers	Fetal Lung	lung
10	chr9:11026200-11026800	Enhancers	Fetal Heart	heart
11	chr9:11026800-11032400	Weak transcription	Fetal Heart	heart
12	chr9:11027000-11027600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr9:11031000-11031400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr9:11031200-11031400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr9:11031400-11032600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr9:11032000-11032200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr9:11032200-11032800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr9:11032400-11033400	Enhancers	Fetal Heart	heart
19	chr9:11032600-11033000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr9:11032600-11033400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr9:11032800-11033200	Active TSS	Fetal Lung	lung
22	chr9:11032800-11033400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr9:11033000-11033200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr9:11033000-11033400	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr9:11033000-11033400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr9:11033200-11038000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr9:11033400-11033600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr9:11033400-11037400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr9:11033400-11037400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr9:11033400-11037800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr9:11033600-11033800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr9:11033600-11037600	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr9:11035600-11037600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr9:11037400-11039600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr9:11037400-11040000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr9:11037600-11039800	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr9:11037600-11040000	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr9:11037600-11040200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr9:11037800-11038400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr9:11037800-11039400	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr9:11038000-11039200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr9:11038400-11038800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr9:11038400-11039400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr9:11039200-11040400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr9:11039600-11040000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr9:11040000-11045000	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr9:11040200-11045400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr9:11041600-11061800	Weak transcription	Hela-S3	cervix
49	chr9:11044800-11063200	Weak transcription	K562	blood
50	chr9:11045000-11045800	Enhancers	HUES64 Cell Line	embryonic stem cell

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