Variant report

Variant	nsv892337
Chromosome Location	chr9:11140883-11404656
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	BHLHE40	chr9:11338205-11338405	GM12878	blood:	n/a	n/a
2	BRCA1	chr9:11272473-11272479	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr9:11319527-11319802	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr9:11269115-11269340	K562	blood:	n/a	n/a
5	CEBPB	chr9:11258134-11258408	HepG2	liver:	n/a	chr9:11258233-11258244
6	CEBPB	chr9:11143408-11143689	A549	lung:	n/a	chr9:11143522-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143523-11143534 chr9:11143524-11143533
7	CEBPB	chr9:11258136-11258368	H1-hESC	embryonic stem cell:	n/a	chr9:11258233-11258244
8	CEBPB	chr9:11143371-11143702	HepG2	liver:	n/a	chr9:11143522-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143523-11143534 chr9:11143524-11143533
9	CEBPB	chr9:11267017-11267301	K562	blood:	n/a	chr9:11267135-11267146
10	CEBPB	chr9:11221528-11221540	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr9:11267004-11267299	HepG2	liver:	n/a	chr9:11267135-11267146
12	CEBPB	chr9:11349171-11349446	HepG2	liver:	n/a	chr9:11349299-11349310
13	CEBPB	chr9:11340836-11340985	A549	lung:	n/a	chr9:11340918-11340929
14	CEBPB	chr9:11258112-11258312	K562	blood:	n/a	chr9:11258233-11258244
15	CEBPB	chr9:11334982-11335237	Hela-S3	cervix:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
16	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
17	CEBPB	chr9:11372456-11372755	HepG2	liver:	n/a	chr9:11372602-11372613
18	CEBPB	chr9:11217166-11217491	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:11357845-11358150	IMR90	lung:	n/a	chr9:11357994-11358007 chr9:11357994-11358005 chr9:11357937-11357948
20	CEBPB	chr9:11258090-11258374	MCF-7	breast:	n/a	chr9:11258233-11258244
21	CEBPB	chr9:11357865-11358142	HepG2	liver:	n/a	chr9:11357994-11358007 chr9:11357994-11358005 chr9:11357937-11357948
22	CEBPB	chr9:11266996-11267317	IMR90	lung:	n/a	chr9:11267135-11267146
23	CEBPB	chr9:11334898-11335195	A549	lung:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
24	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
25	CEBPB	chr9:11257560-11257807	HepG2	liver:	n/a	n/a
26	CEBPB	chr9:11356165-11356517	ECC-1	luminal epithelium:	n/a	chr9:11356437-11356448
27	CEBPB	chr9:11349131-11349344	H1-hESC	embryonic stem cell:	n/a	chr9:11349299-11349310
28	CEBPB	chr9:11334920-11335231	HepG2	liver:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
29	CEBPB	chr9:11294410-11294610	HepG2	liver:	n/a	n/a
30	CEBPB	chr9:11334919-11335258	IMR90	lung:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
31	CEBPB	chr9:11208917-11208996	A549	lung:	n/a	chr9:11208951-11208964
32	CEBPB	chr9:11333545-11333604	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr9:11335919-11336119	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:11221350-11221590	IMR90	lung:	n/a	n/a
35	CEBPB	chr9:11217160-11217484	A549	lung:	n/a	n/a
36	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
37	CEBPB	chr9:11372474-11372712	A549	lung:	n/a	chr9:11372602-11372613
38	CEBPB	chr9:11258112-11258370	A549	lung:	n/a	chr9:11258233-11258244
39	CEBPB	chr9:11258095-11258408	IMR90	lung:	n/a	chr9:11258233-11258244
40	CEBPB	chr9:11340773-11341042	HepG2	liver:	n/a	chr9:11340918-11340929
41	CHD2	chr9:11338305-11338375	GM12878	blood:	n/a	n/a
42	CTCF	chr9:11149440-11149590	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr9:11319540-11319721	SK-N-SH_RA	brain:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
44	CTCF	chr9:11149160-11149310	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr9:11319540-11319690	AG04449	skin:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
46	CTCF	chr9:11319540-11319690	SAEC	small airway:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
47	CTCF	chr9:11319561-11319739	GM13977	blood:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
48	CTCF	chr9:11149174-11149318	GM19238	blood:	n/a	n/a
49	CTCF	chr9:11319560-11319710	GM12864	blood:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658
50	CTCF	chr9:11319544-11319777	MCF-7	breast:	n/a	chr9:11319641-11319657 chr9:11319635-11319656 chr9:11319640-11319658

No.	Distal block	Cell Line	Cell type
1	chr9:11216192..11218001-chr9:11219669..11221559,2	K562	blood:
2	chr9:10855589..10857004-chr9:11319142..11320476,6	MCF-7	breast:
3	chr11:13082457..13083259-chr9:11319197..11319700,2	MCF-7	breast:
4	chr9:10366359..10367238-chr9:11319480..11320059,2	MCF-7	breast:
5	chr1:210502189..210502757-chr9:11220602..11221102,2	HCT-116	colon:
6	chr9:11216192..11218001-chr9:11219669..11221559,2	K562	blood:
7	chr16:12541131..12541857-chr9:11173536..11174397,2	MCF-7	breast:
8	chr9:10855837..10856356-chr9:11319207..11319905,2	MCF-7	breast:

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

Variant related genes	Relation type
ENSG00000230365	TF binding region
ENSG00000054392	chromatin interactions

Extended variants
information (count: 2697 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2697 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7866090	chr9:11140883-11140884	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557840480	chr9:11140927-11140928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10959561	chr9:11140941-11140942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528834897	chr9:11140980-11140981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553973685	chr9:11143894-11143895	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs369347302	chr9:11143907-11143908	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs10116927	chr9:11143915-11143916	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs539177849	chr9:11143941-11143942	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs375697171	chr9:11143950-11143951	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs182964872	chr9:11143997-11143998	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs142729149	chr9:11144004-11144005	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs187217234	chr9:11144011-11144012	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs571024822	chr9:11158234-11158235	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs533300598	chr9:11158235-11158236	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs144935575	chr9:11158263-11158264	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs1931422	chr9:11158296-11158297	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs79450042	chr9:11158309-11158310	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs1931423	chr9:11158314-11158315	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs566235176	chr9:11158318-11158319	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs370630080	chr9:11158325-11158326	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs578220951	chr9:11158326-11158327	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs77238107	chr9:11158332-11158333	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs1931424	chr9:11158345-11158346	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs528655635	chr9:11158386-11158387	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs568614212	chr9:11158418-11158419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551996193	chr9:11158421-11158422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142043766	chr9:11158427-11158428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537707016	chr9:11158429-11158430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs151227778	chr9:11158461-11158462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567291811	chr9:11158463-11158464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1931425	chr9:11158480-11158481	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs553031175	chr9:11158486-11158487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573050074	chr9:11158493-11158494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141389423	chr9:11158557-11158558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557894847	chr9:11158577-11158578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535175548	chr9:11158627-11158628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543673499	chr9:11158641-11158642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188330096	chr9:11158659-11158660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528878880	chr9:11158663-11158664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs180757999	chr9:11158675-11158676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185598181	chr9:11158689-11158690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528229742	chr9:11158692-11158693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs199994971	chr9:11158706-11158707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549572550	chr9:11158731-11158732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571764463	chr9:11158779-11158780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559117829	chr9:11158786-11158787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146986768	chr9:11158796-11158797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147626481	chr9:11158835-11158836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528078090	chr9:11158879-11158880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73641399	chr9:11158900-11158901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:11140000-11141000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:11140600-11141000	Enhancers	Brain Hippocampus Middle	brain
3	chr9:11158200-11158400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:11158200-11158400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr9:11158400-11158800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr9:11158800-11159200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr9:11159200-11160000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr9:11181800-11182400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr9:11194000-11194600	Enhancers	Fetal Brain Male	brain
10	chr9:11194200-11194400	Enhancers	Brain Germinal Matrix	brain
11	chr9:11194200-11195000	Enhancers	Fetal Brain Female	brain
12	chr9:11194400-11195200	Weak transcription	Brain Germinal Matrix	brain
13	chr9:11195200-11196200	Enhancers	Brain Germinal Matrix	brain
14	chr9:11196000-11196800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:11196800-11197200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:11197200-11203000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr9:11199000-11199800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr9:11199200-11199800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr9:11199200-11199800	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr9:11199200-11200400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr9:11199400-11199800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr9:11199600-11200400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr9:11207600-11207800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr9:11233800-11235200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr9:11234600-11235800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr9:11254200-11254800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
27	chr9:11257400-11258600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr9:11257600-11258000	Enhancers	Fetal Heart	heart
29	chr9:11258000-11258400	Flanking Active TSS	Fetal Heart	heart
30	chr9:11258200-11258600	Enhancers	Placenta Amnion	Placenta Amnion
31	chr9:11258200-11258800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr9:11258200-11258800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr9:11258400-11259000	Enhancers	Fetal Heart	heart
34	chr9:11258800-11259800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr9:11259200-11260200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr9:11259400-11259800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr9:11259800-11260000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr9:11268800-11269600	ZNF genes & repeats	Adipose Nuclei	Adipose
39	chr9:11280400-11281000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr9:11280600-11281000	Enhancers	Fetal Brain Female	brain
41	chr9:11280800-11281200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr9:11295400-11297000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr9:11296400-11296600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr9:11296600-11300800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr9:11297000-11297400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
46	chr9:11300800-11301000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr9:11312800-11313600	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr9:11312800-11313600	Enhancers	Brain Hippocampus Middle	brain
49	chr9:11313000-11313400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr9:11313000-11313400	Enhancers	Brain Cingulate Gyrus	brain

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