Variant report

Variant	nsv8415
Chromosome Location	chr9:11173118-11631933
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	chr9:11334982-11335237	Hela-S3	cervix:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
6	CEBPB	chr9:11407895-11408156	IMR90	lung:	n/a	chr9:11408023-11408034 chr9:11408023-11408036
7	CEBPB	chr9:11435034-11435332	H1-hESC	embryonic stem cell:	n/a	chr9:11435176-11435187 chr9:11435176-11435189
8	CEBPB	chr9:11334898-11335195	A549	lung:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
9	CEBPB	chr9:11501534-11501600	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr9:11217160-11217484	A549	lung:	n/a	n/a
11	CEBPB	chr9:11372474-11372712	A549	lung:	n/a	chr9:11372602-11372613
12	CEBPB	chr9:11356165-11356517	ECC-1	luminal epithelium:	n/a	chr9:11356437-11356448
13	CEBPB	chr9:11258090-11258374	MCF-7	breast:	n/a	chr9:11258233-11258244
14	CEBPB	chr9:11597998-11598356	HepG2	liver:	n/a	chr9:11598247-11598258
15	CEBPB	chr9:11266996-11267317	IMR90	lung:	n/a	chr9:11267135-11267146
16	CEBPB	chr9:11258134-11258408	HepG2	liver:	n/a	chr9:11258233-11258244
17	CEBPB	chr9:11457818-11458170	HepG2	liver:	n/a	chr9:11457991-11458008 chr9:11457994-11458007 chr9:11457994-11458005
18	CEBPB	chr9:11457881-11458153	K562	blood:	n/a	chr9:11457991-11458008 chr9:11457994-11458007 chr9:11457994-11458005
19	CEBPB	chr9:11340773-11341042	HepG2	liver:	n/a	chr9:11340918-11340929
20	CEBPB	chr9:11267017-11267301	K562	blood:	n/a	chr9:11267135-11267146
21	CEBPB	chr9:11334919-11335258	IMR90	lung:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
22	CEBPB	chr9:11614215-11614271	K562	blood:	n/a	chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614243-11614254 chr9:11614245-11614256 chr9:11614243-11614256
23	CEBPB	chr9:11221350-11221590	IMR90	lung:	n/a	n/a
24	CEBPB	chr9:11457820-11458148	IMR90	lung:	n/a	chr9:11457991-11458008 chr9:11457994-11458007 chr9:11457994-11458005
25	CEBPB	chr9:11217166-11217491	IMR90	lung:	n/a	n/a
26	CEBPB	chr9:11422396-11422505	HepG2	liver:	n/a	n/a
27	CEBPB	chr9:11407906-11408170	A549	lung:	n/a	chr9:11408023-11408034 chr9:11408023-11408036
28	CEBPB	chr9:11435036-11435322	IMR90	lung:	n/a	chr9:11435176-11435187 chr9:11435176-11435189
29	CEBPB	chr9:11583943-11584270	HepG2	liver:	n/a	chr9:11584097-11584108
30	CEBPB	chr9:11258112-11258312	K562	blood:	n/a	chr9:11258233-11258244
31	CEBPB	chr9:11294410-11294610	HepG2	liver:	n/a	n/a
32	CEBPB	chr9:11267004-11267299	HepG2	liver:	n/a	chr9:11267135-11267146
33	CEBPB	chr9:11349131-11349344	H1-hESC	embryonic stem cell:	n/a	chr9:11349299-11349310
34	CEBPB	chr9:11614083-11614396	A549	lung:	n/a	chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614243-11614254 chr9:11614245-11614256 chr9:11614243-11614256
35	CEBPB	chr9:11372456-11372755	HepG2	liver:	n/a	chr9:11372602-11372613
36	CEBPB	chr9:11593978-11594260	HepG2	liver:	n/a	n/a
37	CEBPB	chr9:11258136-11258368	H1-hESC	embryonic stem cell:	n/a	chr9:11258233-11258244
38	CEBPB	chr9:11434997-11435328	HepG2	liver:	n/a	chr9:11435176-11435187 chr9:11435176-11435189
39	CEBPB	chr9:11457829-11458659	H1-hESC	embryonic stem cell:	n/a	chr9:11457991-11458008 chr9:11457994-11458007 chr9:11458637-11458645 chr9:11457994-11458005
40	CEBPB	chr9:11208917-11208996	A549	lung:	n/a	chr9:11208951-11208964
41	CEBPB	chr9:11333545-11333604	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr9:11614093-11614402	H1-hESC	embryonic stem cell:	n/a	chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614243-11614254 chr9:11614245-11614256 chr9:11614243-11614256
43	CEBPB	chr9:11614116-11614400	HepG2	liver:	n/a	chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614243-11614254 chr9:11614245-11614256 chr9:11614243-11614256
44	CEBPB	chr9:11457812-11458149	A549	lung:	n/a	chr9:11457991-11458008 chr9:11457994-11458007 chr9:11457994-11458005
45	CEBPB	chr9:11349171-11349446	HepG2	liver:	n/a	chr9:11349299-11349310
46	CEBPB	chr9:11334920-11335231	HepG2	liver:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
47	CEBPB	chr9:11335919-11336119	HepG2	liver:	n/a	n/a
48	CEBPB	chr9:11221528-11221540	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr9:11357865-11358142	HepG2	liver:	n/a	chr9:11357994-11358007 chr9:11357994-11358005 chr9:11357937-11357948
50	CEBPB	chr9:11407921-11408170	HepG2	liver:	n/a	chr9:11408023-11408034 chr9:11408023-11408036

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:11618265-11618315	HIPEpiC	eye:	n/a
2	chr9:11618265-11618315	HIPEpiC	eye:	n/a
3	chr9:11618265-11618315	AG09319	gingival:	n/a
4	chr9:11618265-11618315	HRCEpiC	kidney:	n/a
5	chr9:11618691-11618741	A549	lung:	n/a
6	chr9:11618283-11618333	Jurkat	blood:	n/a
7	chr9:11618691-11618741	HCM	heart:	n/a
8	chr9:11618691-11618741	SKMC	muscle:	n/a
9	chr9:11618265-11618315	U87	brain:	n/a
10	chr9:11618265-11618315	Hepatocyte	liver:	n/a
11	chr9:11618283-11618333	BE2_C	brain:	n/a
12	chr9:11618283-11618333	AG04449	skin:	fetal
13	chr9:11618265-11618315	HEEpiC	esophagus:	n/a
14	chr9:11618691-11618741	PrEC	prostate:	n/a
15	chr9:11618691-11618741	HL-60	blood:	n/a
16	chr9:11618691-11618741	HRE	kidney:	n/a
17	chr9:11618283-11618333	GM12891	blood:	n/a
18	chr9:11618283-11618333	Hela-S3	cervix:	n/a
19	chr9:11618283-11618333	NT2-D1	testis:	n/a
20	chr9:11618283-11618333	NHBE	bronchial:	n/a
21	chr9:11618283-11618333	H1-hESC	embryonic stem cell:	embryo
22	chr9:11618283-11618333	K562	blood:	n/a
23	chr9:11618691-11618741	HUVEC	blood vessel:	n/a
24	chr9:11618283-11618333	NH-A	brain:	n/a
25	chr9:11618691-11618741	SK-N-MC	brain:	n/a
26	chr9:11618691-11618741	HCT-116	colon:	n/a
27	chr9:11618265-11618315	PrEC	prostate:	n/a
28	chr9:11618265-11618315	AG10803	skin:	n/a
29	chr9:11618691-11618741	MCF10A-Er-Src	breast:	n/a
30	chr9:11618283-11618333	HCT-116	colon:	n/a
31	chr9:11618691-11618741	NH-A	brain:	n/a
32	chr9:11618691-11618741	GM12891	blood:	n/a
33	chr9:11618691-11618741	AoSMC	blood vessel:	n/a
34	chr9:11618265-11618315	H1-hESC	embryonic stem cell:	embryo
35	chr9:11618691-11618741	NHBE	bronchial:	n/a
36	chr9:11618265-11618315	LNCaP	prostate:	n/a
37	chr9:11618691-11618741	AG04450	lung:	fetal
38	chr9:11618283-11618333	HIPEpiC	eye:	n/a
39	chr9:11618691-11618741	U87	brain:	n/a
40	chr9:11618265-11618315	MCF10A-Er-Src	breast:	n/a
41	chr9:11618691-11618741	K562	blood:	n/a
42	chr9:11618265-11618315	ProgFib	skin:	n/a
43	chr9:11618265-11618315	ECC-1	luminal epithelium:	n/a
44	chr9:11618283-11618333	ovcar-3	ovarian:	n/a
45	chr9:11618691-11618741	NHDF-neo	bronchial:	n/a
46	chr9:11618283-11618333	Hepatocyte	liver:	n/a
47	chr9:11618283-11618333	SAEC	small airway:	n/a
48	chr9:11618265-11618315	GM06990	blood:	n/a
49	chr9:11618265-11618315	PANC-1	pancreas:	n/a
50	chr9:11618265-11618315	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:10855589..10857004-chr9:11319142..11320476,6	MCF-7	breast:
2	chr11:13082457..13083259-chr9:11319197..11319700,2	MCF-7	breast:
3	chr9:10366359..10367238-chr9:11319480..11320059,2	MCF-7	breast:
4	chr11:62609117..62610638-chr9:11453391..11454911,2	K562	blood:
5	chr17:41381793..41383489-chr9:11453391..11454891,3	K562	blood:
6	chr9:11216192..11218001-chr9:11219669..11221559,2	K562	blood:
7	chr9:11216192..11218001-chr9:11219669..11221559,2	K562	blood:
8	chr9:10855837..10856356-chr9:11319207..11319905,2	MCF-7	breast:
9	chr1:210502189..210502757-chr9:11220602..11221102,2	HCT-116	colon:
10	chr16:12541131..12541857-chr9:11173536..11174397,2	MCF-7	breast:

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

Variant related genes	Relation type
ENSG00000230365	TF binding region
ENSG00000230365	CpG island
ENSG00000236383	chromatin interactions
ENSG00000054392	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 6786 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:6786 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140446213	chr9:11181819-11181820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs528018539	chr9:11181827-11181828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182877867	chr9:11181837-11181838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs369968988	chr9:11181880-11181881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539365001	chr9:11181908-11181909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187727135	chr9:11181919-11181920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575734653	chr9:11181920-11181921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs117394775	chr9:11181947-11181948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550983870	chr9:11181952-11181953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554802594	chr9:11181961-11181962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574883013	chr9:11181974-11181975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542411056	chr9:11181978-11181979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143600113	chr9:11181979-11181980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs377293942	chr9:11181987-11181988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191405452	chr9:11182005-11182006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148041127	chr9:11182022-11182023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564518469	chr9:11182028-11182029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2046765	chr9:11182058-11182059	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs12004689	chr9:11182062-11182063	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs560784181	chr9:11182118-11182119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566408494	chr9:11182119-11182120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529802546	chr9:11182120-11182121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184271234	chr9:11182127-11182128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567072296	chr9:11182169-11182170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546298415	chr9:11182218-11182219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552948673	chr9:11182227-11182228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569262818	chr9:11182241-11182242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538199385	chr9:11182243-11182244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548104824	chr9:11182263-11182264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568432986	chr9:11182288-11182289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188613103	chr9:11182308-11182309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12002667	chr9:11182369-11182370	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs192217764	chr9:11182398-11182399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530074699	chr9:11194001-11194002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546691615	chr9:11194005-11194006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142327480	chr9:11194014-11194015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111539129	chr9:11194029-11194030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139000159	chr9:11194052-11194053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs572830390	chr9:11194055-11194056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs10125755	chr9:11194115-11194116	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs565524260	chr9:11194117-11194118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs7465994	chr9:11194132-11194133	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs142144714	chr9:11194149-11194150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567240831	chr9:11194186-11194187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs73403199	chr9:11194222-11194223	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs543906249	chr9:11194236-11194237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10809379	chr9:11194239-11194240	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs146350328	chr9:11194292-11194293	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs529327323	chr9:11194334-11194335	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs559192111	chr9:11194348-11194349	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Schizophrenia	18511947	CNVD

Chromatin state (count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:11181800-11182400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:11194000-11194600	Enhancers	Fetal Brain Male	brain
3	chr9:11194200-11194400	Enhancers	Brain Germinal Matrix	brain
4	chr9:11194200-11195000	Enhancers	Fetal Brain Female	brain
5	chr9:11194400-11195200	Weak transcription	Brain Germinal Matrix	brain
6	chr9:11195200-11196200	Enhancers	Brain Germinal Matrix	brain
7	chr9:11196000-11196800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:11196800-11197200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:11197200-11203000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr9:11199000-11199800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr9:11199200-11199800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr9:11199200-11199800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr9:11199200-11200400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr9:11199400-11199800	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr9:11199600-11200400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr9:11207600-11207800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr9:11233800-11235200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr9:11234600-11235800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr9:11254200-11254800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
20	chr9:11257400-11258600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr9:11257600-11258000	Enhancers	Fetal Heart	heart
22	chr9:11258000-11258400	Flanking Active TSS	Fetal Heart	heart
23	chr9:11258200-11258600	Enhancers	Placenta Amnion	Placenta Amnion
24	chr9:11258200-11258800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr9:11258200-11258800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr9:11258400-11259000	Enhancers	Fetal Heart	heart
27	chr9:11258800-11259800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr9:11259200-11260200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr9:11259400-11259800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr9:11259800-11260000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr9:11268800-11269600	ZNF genes & repeats	Adipose Nuclei	Adipose
32	chr9:11280400-11281000	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr9:11280600-11281000	Enhancers	Fetal Brain Female	brain
34	chr9:11280800-11281200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr9:11295400-11297000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr9:11296400-11296600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr9:11296600-11300800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr9:11297000-11297400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr9:11300800-11301000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr9:11312800-11313600	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr9:11312800-11313600	Enhancers	Brain Hippocampus Middle	brain
42	chr9:11313000-11313400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr9:11313000-11313400	Enhancers	Brain Cingulate Gyrus	brain
44	chr9:11313000-11313600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr9:11313000-11313600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr9:11313000-11313800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr9:11313600-11314600	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr9:11318000-11321800	Enhancers	Fetal Brain Male	brain
49	chr9:11318200-11319200	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr9:11318200-11319800	Enhancers	Fetal Brain Female	brain

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