Variant report

Variant	nsv892333
Chromosome Location	chr9:10957549-11091254
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:322)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:322 , 50 per page) page: 1 2 3 4 5 6 7

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	chr9:11065067-11065094	GM12878	blood:	n/a	n/a
8	BHLHE40	chr9:11064998-11065193	HepG2	liver:	n/a	n/a
9	BHLHE40	chr9:11064885-11065303	K562	blood:	n/a	n/a
10	BRCA1	chr9:11064953-11065285	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr9:11064529-11064729	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr9:11064870-11065315	K562	blood:	n/a	n/a
13	CEBPB	chr9:10997740-10997983	HepG2	liver:	n/a	chr9:10997888-10997899
14	CEBPB	chr9:11084605-11084942	HepG2	liver:	n/a	chr9:11084785-11084796 chr9:11084784-11084797 chr9:11084784-11084795
15	CEBPB	chr9:11084639-11084926	A549	lung:	n/a	chr9:11084785-11084796 chr9:11084784-11084797 chr9:11084784-11084795
16	CEBPB	chr9:11049857-11050082	K562	blood:	n/a	n/a
17	CEBPB	chr9:10978471-10978631	A549	lung:	n/a	chr9:10978574-10978585
18	CEBPB	chr9:11084602-11084944	IMR90	lung:	n/a	chr9:11084785-11084796 chr9:11084784-11084797 chr9:11084784-11084795
19	CEBPB	chr9:10957871-10958258	HepG2	liver:	n/a	chr9:10958059-10958070
20	CEBPB	chr9:10957932-10958241	H1-hESC	embryonic stem cell:	n/a	chr9:10958059-10958070
21	CEBPB	chr9:11022160-11022402	A549	lung:	n/a	chr9:11022289-11022300
22	CEBPB	chr9:10957899-10958248	IMR90	lung:	n/a	chr9:10958059-10958070
23	CEBPB	chr9:10959931-10960102	HepG2	liver:	n/a	chr9:10959996-10960007
24	CEBPB	chr9:10957928-10958232	A549	lung:	n/a	chr9:10958059-10958070
25	CEBPB	chr9:11022159-11022375	HepG2	liver:	n/a	chr9:11022289-11022300
26	CEBPB	chr9:11073722-11074080	A549	lung:	n/a	chr9:11073895-11073908 chr9:11073895-11073906
27	CEBPB	chr9:11073733-11074087	HepG2	liver:	n/a	chr9:11073895-11073908 chr9:11073895-11073906
28	CEBPB	chr9:10997736-10998005	A549	lung:	n/a	chr9:10997888-10997899
29	CEBPB	chr9:11022120-11022420	Hela-S3	cervix:	n/a	chr9:11022289-11022300
30	CEBPB	chr9:10978428-10978694	HepG2	liver:	n/a	chr9:10978574-10978585
31	CEBPB	chr9:11022148-11022435	IMR90	lung:	n/a	chr9:11022289-11022300
32	CEBPB	chr9:11073751-11074022	IMR90	lung:	n/a	chr9:11073895-11073908 chr9:11073895-11073906
33	CEBPB	chr9:10959847-10960172	A549	lung:	n/a	chr9:10959996-10960007
34	CHD2	chr9:11064919-11065283	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr9:11065043-11065254	K562	blood:	n/a	n/a
36	CTCF	chr9:10964233-10964354	Lung_OC	lung:	n/a	n/a
37	CTCF	chr9:11070140-11070290	GM12864	blood:	n/a	n/a
38	CTCF	chr9:11015220-11015370	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr9:11045620-11045770	HEK293	kidney:	n/a	n/a
40	CTCF	chr9:10986506-10986511	LNCaP	prostate:	n/a	n/a
41	CTCF	chr9:11045760-11045910	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr9:10983863-10983874	GM10248	blood:	n/a	n/a
43	CTCF	chr9:11078925-11078952	GM20000	blood:	n/a	n/a
44	CTCF	chr9:11009607-11009644	GM10248	blood:	n/a	n/a
45	CTCF	chr9:10986479-10986499	LNCaP	prostate:	n/a	n/a
46	CTCF	chr9:11026120-11026270	GM12873	blood:	n/a	n/a
47	CTCF	chr9:11049686-11049739	Lung_OC	lung:	n/a	n/a
48	CTCF	chr9:11073600-11073750	GM12870	blood:	n/a	n/a
49	CTCF	chr9:11045680-11045830	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr9:11070225-11070266	Kidney_OC	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:10966083-10966133	MCF-7	breast:	n/a
2	chr9:10966083-10966133	HEEpiC	esophagus:	n/a
3	chr9:10966083-10966133	HAEpiC	amniotic membrane:	n/a
4	chr9:10966083-10966133	U87	brain:	n/a
5	chr9:10966083-10966133	Jurkat	blood:	n/a
6	chr9:10966083-10966133	HCF	heart:	n/a
7	chr9:10966083-10966133	GM19239	blood:	n/a
8	chr9:10966083-10966133	K562	blood:	n/a
9	chr9:10966083-10966133	AG10803	skin:	n/a
10	chr9:10966083-10966133	MCF10A-Er-Src	breast:	n/a
11	chr9:10966083-10966133	SK-N-SH	brain:	n/a
12	chr9:10966083-10966133	SK-N-SH_RA	brain:	n/a
13	chr9:10966083-10966133	H1-hESC	embryonic stem cell:	embryo
14	chr9:10966083-10966133	HepG2	liver:	n/a
15	chr9:10966083-10966133	Hepatocyte	liver:	n/a
16	chr9:10966083-10966133	SK-N-MC	brain:	n/a
17	chr9:10966083-10966133	NHBE	bronchial:	n/a
18	chr9:10966083-10966133	GM06990	blood:	n/a
19	chr9:10966083-10966133	NHDF-neo	bronchial:	n/a
20	chr9:10966083-10966133	NT2-D1	testis:	n/a
21	chr9:10966083-10966133	BE2_C	brain:	n/a
22	chr9:10966083-10966133	HL-60	blood:	n/a
23	chr9:10966083-10966133	HPAEpiC	pulmonary alveolar:	n/a
24	chr9:10966083-10966133	ECC-1	luminal epithelium:	n/a
25	chr9:10966083-10966133	AG04450	lung:	fetal
26	chr9:10966083-10966133	HUVEC	blood vessel:	n/a
27	chr9:10966083-10966133	AG09309	skin:	n/a
28	chr9:10966083-10966133	A549	lung:	n/a
29	chr9:10966083-10966133	HRCEpiC	kidney:	n/a
30	chr9:10966083-10966133	SKMC	muscle:	n/a
31	chr9:10966083-10966133	HNPCEpiC	eye:	n/a
32	chr9:10966083-10966133	NH-A	brain:	n/a
33	chr9:10966083-10966133	Hela-S3	cervix:	n/a
34	chr9:10966083-10966133	GM12891	blood:	n/a
35	chr9:10966083-10966133	SAEC	small airway:	n/a
36	chr9:10966083-10966133	PrEC	prostate:	n/a
37	chr9:10966083-10966133	AG04449	skin:	fetal
38	chr9:10966083-10966133	HIPEpiC	eye:	n/a
39	chr9:10966083-10966133	HCT-116	colon:	n/a
40	chr9:10966083-10966133	BJ	skin:	n/a
41	chr9:10966083-10966133	CMK	blood:	n/a
42	chr9:10966083-10966133	Caco-2	colon:	n/a
43	chr9:10966083-10966133	HCM	heart:	n/a
44	chr9:10966083-10966133	GM12892	blood:	n/a
45	chr9:10966083-10966133	GM12878	blood:	n/a
46	chr9:10966083-10966133	HMEC	breast:	n/a
47	chr9:10966083-10966133	IMR90	lung:	fetal
48	chr9:10966083-10966133	ovcar-3	ovarian:	n/a
49	chr9:10966083-10966133	HRE	kidney:	n/a
50	chr9:10966083-10966133	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:11056337..11059587-chr9:11061284..11064646,4	K562	blood:
2	chr9:11026162..11028762-chr9:11041183..11043715,2	K562	blood:
3	chr9:11059291..11061789-chr9:11063668..11065240,2	MCF-7	breast:
4	chr9:11018319..11020122-chr9:11028284..11030426,2	K562	blood:
5	chr9:11047509..11049109-chr9:11061184..11063575,2	MCF-7	breast:
6	chr9:11056159..11057837-chr9:11062194..11064646,2	K562	blood:
7	chr9:11051115..11054715-chr9:11062496..11065504,4	K562	blood:
8	chr9:11064416..11066663-chr9:11091382..11093294,2	MCF-7	breast:
9	chr9:11052013..11055648-chr9:11062078..11065783,4	K562	blood:
10	chr9:11047082..11049411-chr9:11061377..11064321,2	K562	blood:
11	chr9:11018319..11020122-chr9:11028284..11030426,2	K562	blood:
12	chr9:11026162..11028762-chr9:11041183..11043715,2	K562	blood:
13	chr9:11049044..11051208-chr9:11053146..11055450,2	K562	blood:
14	chr9:11047509..11049109-chr9:11061184..11063575,2	MCF-7	breast:
15	chr9:11053156..11054741-chr9:11055812..11058059,2	K562	blood:
16	chr9:11059291..11061789-chr9:11063668..11065240,2	MCF-7	breast:
17	chr9:11047082..11049411-chr9:11061377..11064321,2	K562	blood:
18	chr9:11052013..11055648-chr9:11062078..11065783,4	K562	blood:
19	chr9:11063987..11066726-chr9:11070793..11073075,2	MCF-7	breast:
20	chr9:11039996..11042346-chr9:11065271..11066776,2	K562	blood:
21	chr9:11039996..11042346-chr9:11065271..11066776,2	K562	blood:
22	chr9:11044597..11046205-chr9:11057945..11060223,2	MCF-7	breast:
23	chr9:11056337..11059587-chr9:11061284..11064646,4	K562	blood:
24	chr9:11051115..11054715-chr9:11062496..11065504,4	K562	blood:
25	chr9:11063987..11066726-chr9:11070793..11073075,2	MCF-7	breast:
26	chr9:11044597..11046205-chr9:11057945..11060223,2	MCF-7	breast:
27	chr9:11053156..11054741-chr9:11055812..11058059,2	K562	blood:
28	chr9:11049044..11051208-chr9:11053146..11055450,2	K562	blood:
29	chr9:11056159..11057837-chr9:11062194..11064646,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRD-7	chr9:10958410-10958540	NONHSAT130207

No data

Variant related genes	Relation type
ENSG00000234146	TF binding region
ENSG00000234146	CpG island

Extended variants
information (count: 2880 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:2880 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528922859	chr9:10958442-10958443	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs373977015	chr9:10958450-10958451	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs7863650	chr9:10958468-10958469	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs35040619	chr9:10958483-10958484	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs565780343	chr9:10958485-10958486	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs534861236	chr9:10958490-10958491	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs79874657	chr9:10958526-10958527	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs76280320	chr9:10958527-10958528	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs78868676	chr9:10958528-10958529	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs545716594	chr9:10999628-10999629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556386570	chr9:10999646-10999647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs72706899	chr9:10999687-10999688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs61655690	chr9:10999750-10999751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145607009	chr9:10999758-10999759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567755545	chr9:10999767-10999768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561353420	chr9:10999778-10999779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527327069	chr9:10999800-10999801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575816601	chr9:10999809-10999810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540723921	chr9:10999838-10999839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182324159	chr9:10999839-10999840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544443120	chr9:10999892-10999893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs55709020	chr9:10999899-10999900	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs547732234	chr9:10999913-10999914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10959445	chr9:10999923-10999924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147714064	chr9:10999932-10999933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377133055	chr9:10999941-10999942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186633761	chr9:10999944-10999945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549741270	chr9:10999981-10999982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566079234	chr9:10999989-10999990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540323615	chr9:11000004-11000005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535048923	chr9:11000046-11000047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551839933	chr9:11000059-11000060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571664221	chr9:11000067-11000068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560201612	chr9:11000121-11000122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201723230	chr9:11000219-11000220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532101464	chr9:11000227-11000228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192755401	chr9:11000232-11000233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79513978	chr9:11000315-11000316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556084661	chr9:11000392-11000393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370553039	chr9:11000411-11000412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140437110	chr9:11000416-11000417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144271132	chr9:11000434-11000435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs151148839	chr9:11000440-11000441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs117572986	chr9:11000499-11000500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184757781	chr9:11000502-11000503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564180890	chr9:11000506-11000507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140043807	chr9:11000514-11000515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543955396	chr9:11000539-11000540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563722658	chr9:11000561-11000562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1330250	chr9:11000575-11000576	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:108)

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

Chromatin state (count:105 , 50 per page) page: 1 2 3

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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