Variant report

Variant	nsv892572
Chromosome Location	chr9:12549675-12715816
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	chr9:12702242-12702514	HepG2	liver:	n/a	n/a
2	ATF3	chr9:12708586-12708908	HCT-116	colon:	n/a	n/a
3	BACH1	chr9:12653013-12653212	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:12567176-12567212	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:12604207-12604421	H1-hESC	embryonic stem cell:	n/a	chr9:12604278-12604292
6	BHLHE40	chr9:12612186-12612202	GM12878	blood:	n/a	n/a
7	BRCA1	chr9:12666817-12666918	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr9:12708489-12709018	HCT-116	colon:	n/a	n/a
9	CEBPB	chr9:12643730-12643980	IMR90	lung:	n/a	n/a
10	CEBPB	chr9:12656839-12657163	K562	blood:	n/a	chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988
11	CEBPB	chr9:12656859-12657130	Hela-S3	cervix:	n/a	chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988
12	CEBPB	chr9:12702155-12702522	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr9:12656816-12657170	A549	lung:	n/a	chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988
14	CEBPB	chr9:12712576-12712881	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr9:12681461-12681946	IMR90	lung:	n/a	chr9:12681604-12681615
16	CEBPB	chr9:12702101-12702516	A549	lung:	n/a	n/a
17	CEBPB	chr9:12702160-12702495	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:12553807-12553971	HepG2	liver:	n/a	chr9:12553921-12553932 chr9:12553919-12553930
19	CEBPB	chr9:12690390-12690469	K562	blood:	n/a	chr9:12690390-12690401 chr9:12690390-12690403 chr9:12690390-12690403 chr9:12690390-12690403
20	CEBPB	chr9:12681521-12681770	A549	lung:	n/a	chr9:12681604-12681615
21	CEBPB	chr9:12708437-12709072	HCT-116	colon:	n/a	chr9:12708963-12708975 chr9:12708893-12708906
22	CEBPB	chr9:12712587-12712868	HepG2	liver:	n/a	n/a
23	CEBPB	chr9:12681514-12681726	HepG2	liver:	n/a	chr9:12681604-12681615
24	CEBPB	chr9:12607483-12607778	IMR90	lung:	n/a	chr9:12607616-12607627 chr9:12607571-12607582
25	CEBPB	chr9:12712648-12712865	A549	lung:	n/a	n/a
26	CEBPB	chr9:12656603-12657162	IMR90	lung:	n/a	chr9:12656979-12656988 chr9:12656681-12656694 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656681-12656692 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988 chr9:12656681-12656694
27	CEBPB	chr9:12690305-12690523	IMR90	lung:	n/a	chr9:12690390-12690401 chr9:12690390-12690403 chr9:12690390-12690403 chr9:12690390-12690403
28	CEBPB	chr9:12698242-12698670	IMR90	lung:	n/a	n/a
29	CEBPB	chr9:12702152-12702503	A549	lung:	n/a	n/a
30	CEBPB	chr9:12681436-12681753	ECC-1	luminal epithelium:	n/a	chr9:12681604-12681615
31	CEBPB	chr9:12656840-12657079	H1-hESC	embryonic stem cell:	n/a	chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988
32	CEBPB	chr9:12607448-12607767	HepG2	liver:	n/a	chr9:12607616-12607627 chr9:12607571-12607582
33	CEBPB	chr9:12681471-12681796	Hela-S3	cervix:	n/a	chr9:12681604-12681615
34	CEBPB	chr9:12708594-12708912	Hela-S3	cervix:	n/a	chr9:12708893-12708906
35	CEBPB	chr9:12656586-12657172	HepG2	liver:	n/a	chr9:12656979-12656988 chr9:12656681-12656694 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656681-12656692 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988 chr9:12656681-12656694
36	CEBPB	chr9:12708603-12708891	IMR90	lung:	n/a	n/a
37	CEBPB	chr9:12553870-12554030	IMR90	lung:	n/a	chr9:12553921-12553932 chr9:12553919-12553930
38	CEBPB	chr9:12676985-12677220	HepG2	liver:	n/a	chr9:12677146-12677157 chr9:12677068-12677076
39	CTCF	chr9:12640180-12640330	HUVEC	blood vessel:	n/a	chr9:12640209-12640222 chr9:12640207-12640225 chr9:12640202-12640223
40	CTCF	chr9:12666966-12667074	GM13977	blood:	n/a	n/a
41	CTCF	chr9:12640140-12640290	HRE	kidney:	n/a	chr9:12640209-12640222 chr9:12640207-12640225 chr9:12640202-12640223
42	CTCF	chr9:12699120-12699270	AG04449	skin:	n/a	n/a
43	CTCF	chr9:12699620-12699770	MCF-7	breast:	n/a	n/a
44	CTCF	chr9:12666993-12667048	GM20000	blood:	n/a	n/a
45	CTCF	chr9:12666942-12667105	Gliobla	brain:	n/a	n/a
46	CTCF	chr9:12640160-12640310	HVMF	connective:	n/a	chr9:12640209-12640222 chr9:12640207-12640225 chr9:12640202-12640223
47	CTCF	chr9:12640120-12640270	HFF-Myc	foreskin:	n/a	chr9:12640209-12640222 chr9:12640207-12640225 chr9:12640202-12640223
48	CTCF	chr9:12699660-12699810	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr9:12699640-12699790	SAEC	small airway:	n/a	n/a
50	CTCF	chr9:12666907-12667129	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:12704964-12705014	PFSK-1	brain:	n/a
2	chr9:12704964-12705014	PFSK-1	brain:	n/a
3	chr9:12704964-12705014	NB4	blood:	n/a
4	chr9:12693694-12693744	MCF-7	breast:	n/a
5	chr9:12693694-12693744	Hepatocyte	liver:	n/a
6	chr9:12704964-12705014	AG04450	lung:	fetal
7	chr9:12693326-12693376	GM12892	blood:	n/a
8	chr9:12693326-12693376	HNPCEpiC	eye:	n/a
9	chr9:12693326-12693376	U87	brain:	n/a
10	chr9:12693326-12693376	IMR90	lung:	fetal
11	chr9:12693694-12693744	ProgFib	skin:	n/a
12	chr9:12693694-12693744	GM06990	blood:	n/a
13	chr9:12693326-12693376	HAEpiC	amniotic membrane:	n/a
14	chr9:12693326-12693376	K562	blood:	n/a
15	chr9:12693694-12693744	ovcar-3	ovarian:	n/a
16	chr9:12693326-12693376	GM12878	blood:	n/a
17	chr9:12704964-12705014	A549	lung:	n/a
18	chr9:12693326-12693376	SKMC	muscle:	n/a
19	chr9:12693694-12693744	NH-A	brain:	n/a
20	chr9:12693326-12693376	MCF-7	breast:	n/a
21	chr9:12693326-12693376	HCF	heart:	n/a
22	chr9:12704964-12705014	HMEC	breast:	n/a
23	chr9:12693326-12693376	HRE	kidney:	n/a
24	chr9:12693694-12693744	AoSMC	blood vessel:	n/a
25	chr9:12704964-12705014	HCT-116	colon:	n/a
26	chr9:12693326-12693376	LNCaP	prostate:	n/a
27	chr9:12693694-12693744	HRE	kidney:	n/a
28	chr9:12704964-12705014	H1-hESC	embryonic stem cell:	embryo
29	chr9:12704964-12705014	RPTEC	kidney:	n/a
30	chr9:12693694-12693744	GM19239	blood:	n/a
31	chr9:12704964-12705014	K562	blood:	n/a
32	chr9:12693326-12693376	PrEC	prostate:	n/a
33	chr9:12704964-12705014	Jurkat	blood:	n/a
34	chr9:12693326-12693376	Jurkat	blood:	n/a
35	chr9:12704964-12705014	AG04449	skin:	fetal
36	chr9:12693326-12693376	NH-A	brain:	n/a
37	chr9:12704964-12705014	AoSMC	blood vessel:	n/a
38	chr9:12704964-12705014	HCM	heart:	n/a
39	chr9:12693326-12693376	SK-N-MC	brain:	n/a
40	chr9:12693694-12693744	HNPCEpiC	eye:	n/a
41	chr9:12693694-12693744	SK-N-MC	brain:	n/a
42	chr9:12693694-12693744	AG10803	skin:	n/a
43	chr9:12704964-12705014	CMK	blood:	n/a
44	chr9:12693326-12693376	GM06990	blood:	n/a
45	chr9:12693326-12693376	AG04450	lung:	fetal
46	chr9:12704964-12705014	BE2_C	brain:	n/a
47	chr9:12693326-12693376	PFSK-1	brain:	n/a
48	chr9:12704964-12705014	AG09319	gingival:	n/a
49	chr9:12693326-12693376	AG09319	gingival:	n/a
50	chr9:12693694-12693744	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:12554435..12555308-chr9:12639713..12640600,2	MCF-7	breast:
2	chr9:12607055..12609983-chr9:12671838..12674027,2	K562	blood:
3	chr9:12607055..12609983-chr9:12671838..12674027,2	K562	blood:
4	chr9:12615022..12617476-chr9:12617492..12619010,2	MCF-7	breast:
5	chr9:12554435..12555308-chr9:12639713..12640600,2	MCF-7	breast:
6	chr9:12715023..12717622-chr9:12718396..12720573,2	MCF-7	breast:
7	chr9:12694806..12696732-chr9:12696808..12698503,2	MCF-7	breast:
8	chr9:12708111..12711033-chr9:13076014..13078647,2	MCF-7	breast:
9	chr9:12615022..12617476-chr9:12617492..12619010,2	MCF-7	breast:
10	chr9:12631997..12633907-chr9:12634270..12637039,2	MCF-7	breast:
11	chr9:12709414..12711296-chr9:14429666..14432393,2	MCF-7	breast:
12	chr9:12631997..12633907-chr9:12634270..12637039,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf150-4	chr9:12693309-12693478	NONHSAT130224
2	lnc-C9orf150-4	chr9:12693912-12694487	NONHSAT130224
3	lnc-MPDZ-1	chr9:12700100-12700626	ENSG00000235448.1

Variant related genes	Relation type
TYRP1	TF binding region
TYRP1	CpG island
ENSG00000107165	chromatin interactions

Extended variants
information (count: 4498 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:4498 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146375365	chr9:12555408-12555409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574984711	chr9:12555429-12555430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187784226	chr9:12555435-12555436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148161174	chr9:12555456-12555457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142020308	chr9:12555510-12555511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547221832	chr9:12555562-12555563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536766002	chr9:12555573-12555574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189868850	chr9:12555590-12555591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371379710	chr9:12555592-12555593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539257128	chr9:12555618-12555619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182130834	chr9:12555629-12555630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187238303	chr9:12555633-12555634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs199774570	chr9:12555637-12555638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs34515958	chr9:12555638-12555639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536637862	chr9:12555647-12555648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534216008	chr9:12555691-12555692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555628359	chr9:12555754-12555755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs111940357	chr9:12555832-12555833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191696083	chr9:12555853-12555854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534150005	chr9:12555857-12555858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148508523	chr9:12555867-12555868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs150606375	chr9:12555949-12555950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577378032	chr9:12555954-12555955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376980137	chr9:12555999-12556000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546442007	chr9:12556016-12556017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185297906	chr9:12556027-12556028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188612833	chr9:12556061-12556062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576562673	chr9:12556082-12556083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs193145660	chr9:12556117-12556118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562401591	chr9:12556118-12556119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368536816	chr9:12556140-12556141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527289178	chr9:12556194-12556195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139697403	chr9:12556199-12556200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75253467	chr9:12556241-12556242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149785748	chr9:12556244-12556245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372630817	chr9:12556290-12556291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185698183	chr9:12556291-12556292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373210453	chr9:12556302-12556303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376611591	chr9:12556327-12556328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200344035	chr9:12556336-12556337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190222099	chr9:12556377-12556378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs180893889	chr9:12556406-12556407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147482226	chr9:12556411-12556412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140022589	chr9:12556412-12556413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554182792	chr9:12556474-12556475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183522163	chr9:12556479-12556480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369087963	chr9:12556507-12556508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539972929	chr9:12556516-12556517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145219211	chr9:12556559-12556560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576607067	chr9:12556566-12556567	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
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
abnormal development	18461090	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD
Chordoma	21215367	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12555400-12556200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:12555400-12556800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr9:12559600-12560000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:12560000-12560400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr9:12566800-12567400	Enhancers	Stomach Mucosa	stomach
6	chr9:12595600-12596000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:12598800-12599800	Enhancers	Fetal Heart	heart
8	chr9:12599800-12604000	Weak transcription	Fetal Heart	heart
9	chr9:12604000-12604400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr9:12604000-12604600	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr9:12604000-12604600	Enhancers	HMEC	breast
12	chr9:12604000-12605200	Enhancers	Fetal Heart	heart
13	chr9:12604000-12605200	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr9:12604200-12604600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr9:12604200-12604600	Enhancers	Psoas Muscle	Psoas
16	chr9:12604600-12605800	Weak transcription	Psoas Muscle	Psoas
17	chr9:12606000-12606200	Enhancers	Psoas Muscle	Psoas
18	chr9:12612200-12613000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr9:12612600-12613800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr9:12615600-12615800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:12615600-12615800	Enhancers	Fetal Lung	lung
22	chr9:12615800-12616600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:12616600-12617200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:12624600-12625000	Enhancers	Fetal Kidney	kidney
25	chr9:12625000-12629200	Weak transcription	Fetal Kidney	kidney
26	chr9:12626600-12626800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr9:12626800-12627800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr9:12626800-12629000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr9:12627000-12627600	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr9:12627000-12627800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr9:12627000-12627800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr9:12627200-12627400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr9:12627200-12627800	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr9:12627400-12628800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr9:12627600-12627800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr9:12627600-12627800	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr9:12627600-12628000	Enhancers	H1 Cell Line	embryonic stem cell
38	chr9:12627600-12629000	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr9:12627800-12628000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr9:12627800-12628000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr9:12627800-12629000	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr9:12627800-12629000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr9:12627800-12629000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr9:12627800-12629400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr9:12628000-12629000	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr9:12628000-12629000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr9:12628800-12630000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr9:12628800-12630200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr9:12629000-12630000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr9:12629000-12630000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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