Variant report

Variant	nsv1016570
Chromosome Location	chr9:12576095-12722387
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	chr9:12719466-12719806	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:12702242-12702514	HepG2	liver:	n/a	n/a
3	ATF3	chr9:12708586-12708908	HCT-116	colon:	n/a	n/a
4	BACH1	chr9:12653013-12653212	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	chr9:12702101-12702516	A549	lung:	n/a	n/a
10	CEBPB	chr9:12712576-12712881	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr9:12708437-12709072	HCT-116	colon:	n/a	chr9:12708963-12708975 chr9:12708893-12708906
12	CEBPB	chr9:12698242-12698670	IMR90	lung:	n/a	n/a
13	CEBPB	chr9:12607483-12607778	IMR90	lung:	n/a	chr9:12607616-12607627 chr9:12607571-12607582
14	CEBPB	chr9:12681461-12681946	IMR90	lung:	n/a	chr9:12681604-12681615
15	CEBPB	chr9:12702152-12702503	A549	lung:	n/a	n/a
16	CEBPB	chr9:12718687-12719000	H1-hESC	embryonic stem cell:	n/a	chr9:12718859-12718870
17	CEBPB	chr9:12712587-12712868	HepG2	liver:	n/a	n/a
18	CEBPB	chr9:12712648-12712865	A549	lung:	n/a	n/a
19	CEBPB	chr9:12607448-12607767	HepG2	liver:	n/a	chr9:12607616-12607627 chr9:12607571-12607582
20	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
21	CEBPB	chr9:12708594-12708912	Hela-S3	cervix:	n/a	chr9:12708893-12708906
22	CEBPB	chr9:12643730-12643980	IMR90	lung:	n/a	n/a
23	CEBPB	chr9:12676985-12677220	HepG2	liver:	n/a	chr9:12677146-12677157 chr9:12677068-12677076
24	CEBPB	chr9:12681436-12681753	ECC-1	luminal epithelium:	n/a	chr9:12681604-12681615
25	CEBPB	chr9:12681514-12681726	HepG2	liver:	n/a	chr9:12681604-12681615
26	CEBPB	chr9:12702155-12702522	Hela-S3	cervix:	n/a	n/a
27	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
28	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
29	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
30	CEBPB	chr9:12690390-12690469	K562	blood:	n/a	chr9:12690390-12690401 chr9:12690390-12690403 chr9:12690390-12690403 chr9:12690390-12690403
31	CEBPB	chr9:12708603-12708891	IMR90	lung:	n/a	n/a
32	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
33	CEBPB	chr9:12690305-12690523	IMR90	lung:	n/a	chr9:12690390-12690401 chr9:12690390-12690403 chr9:12690390-12690403 chr9:12690390-12690403
34	CEBPB	chr9:12681521-12681770	A549	lung:	n/a	chr9:12681604-12681615
35	CEBPB	chr9:12681471-12681796	Hela-S3	cervix:	n/a	chr9:12681604-12681615
36	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
37	CEBPB	chr9:12702160-12702495	IMR90	lung:	n/a	n/a
38	CTCF	chr9:12640060-12640210	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr9:12666927-12667111	GM12878	blood:	n/a	n/a
40	CTCF	chr9:12639555-12640597	A549	lung:	n/a	chr9:12640209-12640222 chr9:12640207-12640225 chr9:12640202-12640223
41	CTCF	chr9:12702143-12702536	IMR90	lung:	n/a	n/a
42	CTCF	chr9:12702260-12702410	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr9:12640071-12640264	A549	lung:	n/a	chr9:12640209-12640222 chr9:12640207-12640225 chr9:12640202-12640223
44	CTCF	chr9:12716980-12717130	HPAF	blood vessel:	n/a	chr9:12717026-12717044 chr9:12717027-12717043 chr9:12717028-12717049
45	CTCF	chr9:12716720-12716870	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr9:12640140-12640290	GM12864	blood:	n/a	chr9:12640209-12640222 chr9:12640207-12640225 chr9:12640202-12640223
47	CTCF	chr9:12640133-12640310	Spleen_OC	spleen:	n/a	chr9:12640209-12640222 chr9:12640207-12640225 chr9:12640202-12640223
48	CTCF	chr9:12702300-12702450	AG09319	gingival:	n/a	n/a
49	CTCF	chr9:12698880-12699030	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr9:12719540-12719690	NB4	blood:	n/a	chr9:12719630-12719651 chr9:12719628-12719646

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:12693694-12693744	GM12878	blood:	n/a
2	chr9:12693694-12693744	RPTEC	kidney:	n/a
3	chr9:12693326-12693376	HRCEpiC	kidney:	n/a
4	chr9:12693694-12693744	GM06990	blood:	n/a
5	chr9:12704964-12705014	NT2-D1	testis:	n/a
6	chr9:12693326-12693376	GM06990	blood:	n/a
7	chr9:12704964-12705014	NHBE	bronchial:	n/a
8	chr9:12693326-12693376	ECC-1	luminal epithelium:	n/a
9	chr9:12693326-12693376	PFSK-1	brain:	n/a
10	chr9:12693694-12693744	GM19239	blood:	n/a
11	chr9:12704964-12705014	HCF	heart:	n/a
12	chr9:12693326-12693376	ovcar-3	ovarian:	n/a
13	chr9:12693326-12693376	HEEpiC	esophagus:	n/a
14	chr9:12693694-12693744	HEK293	kidney:	embryo
15	chr9:12693694-12693744	HCT-116	colon:	n/a
16	chr9:12704964-12705014	SK-N-SH_RA	brain:	n/a
17	chr9:12693326-12693376	HPAEpiC	pulmonary alveolar:	n/a
18	chr9:12704964-12705014	NB4	blood:	n/a
19	chr9:12693326-12693376	SK-N-SH	brain:	n/a
20	chr9:12693326-12693376	K562	blood:	n/a
21	chr9:12693694-12693744	K562	blood:	n/a
22	chr9:12704964-12705014	HEEpiC	esophagus:	n/a
23	chr9:12704964-12705014	PANC-1	pancreas:	n/a
24	chr9:12693326-12693376	MCF-7	breast:	n/a
25	chr9:12693326-12693376	GM12892	blood:	n/a
26	chr9:12693694-12693744	HUVEC	blood vessel:	n/a
27	chr9:12704964-12705014	HepG2	liver:	n/a
28	chr9:12693326-12693376	AG09319	gingival:	n/a
29	chr9:12704964-12705014	BE2_C	brain:	n/a
30	chr9:12704964-12705014	HPAEpiC	pulmonary alveolar:	n/a
31	chr9:12693326-12693376	NB4	blood:	n/a
32	chr9:12693694-12693744	BJ	skin:	n/a
33	chr9:12693326-12693376	HL-60	blood:	n/a
34	chr9:12704964-12705014	HCM	heart:	n/a
35	chr9:12704964-12705014	HEK293	kidney:	embryo
36	chr9:12693326-12693376	MCF10A-Er-Src	breast:	n/a
37	chr9:12693326-12693376	PANC-1	pancreas:	n/a
38	chr9:12693694-12693744	ovcar-3	ovarian:	n/a
39	chr9:12704964-12705014	HRCEpiC	kidney:	n/a
40	chr9:12704964-12705014	H1-hESC	embryonic stem cell:	embryo
41	chr9:12704964-12705014	GM12892	blood:	n/a
42	chr9:12704964-12705014	BJ	skin:	n/a
43	chr9:12704964-12705014	PrEC	prostate:	n/a
44	chr9:12693326-12693376	HUVEC	blood vessel:	n/a
45	chr9:12693694-12693744	GM12891	blood:	n/a
46	chr9:12693326-12693376	Hela-S3	cervix:	n/a
47	chr9:12693326-12693376	BE2_C	brain:	n/a
48	chr9:12693326-12693376	SAEC	small airway:	n/a
49	chr9:12693326-12693376	HRPEpiC	eye:	n/a
50	chr9:12693326-12693376	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:12719485..12720037-chr9:12987933..12988498,2	MCF-7	breast:
2	chr9:12716514..12718700-chr9:12776478..12778096,2	MCF-7	breast:
3	chr9:12719062..12719862-chr9:12884578..12885277,2	MCF-7	breast:
4	chr9:12615022..12617476-chr9:12617492..12619010,2	MCF-7	breast:
5	chr9:12631997..12633907-chr9:12634270..12637039,2	MCF-7	breast:
6	chr9:12715023..12717622-chr9:12718396..12720573,2	MCF-7	breast:
7	chr9:12715023..12717622-chr9:12718396..12720573,2	MCF-7	breast:
8	chr9:12694806..12696732-chr9:12696808..12698503,2	MCF-7	breast:
9	chr9:12607055..12609983-chr9:12671838..12674027,2	K562	blood:
10	chr9:12554435..12555308-chr9:12639713..12640600,2	MCF-7	breast:
11	chr9:12615022..12617476-chr9:12617492..12619010,2	MCF-7	breast:
12	chr9:12709414..12711296-chr9:14429666..14432393,2	MCF-7	breast:
13	chr9:12708111..12711033-chr9:13076014..13078647,2	MCF-7	breast:
14	chr9:12607055..12609983-chr9:12671838..12674027,2	K562	blood:
15	chr9:12631997..12633907-chr9:12634270..12637039,2	MCF-7	breast:
16	chr9:12722041..12725292-chr9:12774361..12778280,6	MCF-7	breast:

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

Variant related genes	Relation type
TYRP1	TF binding region
TYRP1	CpG island
ENSG00000153714	chromatin interactions
ENSG00000107165	chromatin interactions

Extended variants
information (count: 4642 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:4642 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547251670	chr9:12595605-12595606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs116213293	chr9:12595616-12595617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538643610	chr9:12595617-12595618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376454833	chr9:12595660-12595661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150466112	chr9:12595711-12595712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533878049	chr9:12595712-12595713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574996317	chr9:12595738-12595739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539143553	chr9:12595749-12595750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182677582	chr9:12595790-12595791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554382328	chr9:12595803-12595804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187805352	chr9:12595811-12595812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540183589	chr9:12595841-12595842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs201057630	chr9:12595865-12595866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs201879293	chr9:12595866-12595867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77961228	chr9:12595879-12595880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs71507323	chr9:12595889-12595890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs79376660	chr9:12595906-12595907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545425252	chr9:12595915-12595916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs118073831	chr9:12595947-12595948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531069070	chr9:12595950-12595951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189436470	chr9:12598824-12598825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144010408	chr9:12598842-12598843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574785517	chr9:12598856-12598857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34803310	chr9:12598870-12598871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570500664	chr9:12598877-12598878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539575537	chr9:12598888-12598889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540306459	chr9:12598907-12598908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553882215	chr9:12598917-12598918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556262902	chr9:12598955-12598956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570101736	chr9:12598963-12598964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535683106	chr9:12598967-12598968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371933164	chr9:12599022-12599023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555882688	chr9:12599041-12599042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182068930	chr9:12599074-12599075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576940032	chr9:12599080-12599081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545566012	chr9:12599084-12599085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146449959	chr9:12599121-12599122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557820446	chr9:12599151-12599152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529740114	chr9:12599156-12599157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs577688972	chr9:12599183-12599184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573847643	chr9:12599228-12599229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376371802	chr9:12599230-12599231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114661447	chr9:12599266-12599267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542458043	chr9:12599286-12599287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559493844	chr9:12599292-12599293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528412714	chr9:12599300-12599301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551242479	chr9:12599338-12599339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542134310	chr9:12599383-12599384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562545580	chr9:12599386-12599387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs367958791	chr9:12599388-12599389	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
Renal cell carcinoma	21215367	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	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:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12595600-12596000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr9:12598800-12599800	Enhancers	Fetal Heart	heart
3	chr9:12599800-12604000	Weak transcription	Fetal Heart	heart
4	chr9:12604000-12604400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:12604000-12604600	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr9:12604000-12604600	Enhancers	HMEC	breast
7	chr9:12604000-12605200	Enhancers	Fetal Heart	heart
8	chr9:12604000-12605200	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr9:12604200-12604600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr9:12604200-12604600	Enhancers	Psoas Muscle	Psoas
11	chr9:12604600-12605800	Weak transcription	Psoas Muscle	Psoas
12	chr9:12606000-12606200	Enhancers	Psoas Muscle	Psoas
13	chr9:12612200-12613000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr9:12612600-12613800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr9:12615600-12615800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr9:12615600-12615800	Enhancers	Fetal Lung	lung
17	chr9:12615800-12616600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr9:12616600-12617200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr9:12624600-12625000	Enhancers	Fetal Kidney	kidney
20	chr9:12625000-12629200	Weak transcription	Fetal Kidney	kidney
21	chr9:12626600-12626800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr9:12626800-12627800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr9:12626800-12629000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr9:12627000-12627600	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr9:12627000-12627800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr9:12627000-12627800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr9:12627200-12627400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr9:12627200-12627800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr9:12627400-12628800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr9:12627600-12627800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr9:12627600-12627800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr9:12627600-12628000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr9:12627600-12629000	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr9:12627800-12628000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr9:12627800-12628000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr9:12627800-12629000	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr9:12627800-12629000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr9:12627800-12629000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr9:12627800-12629400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr9:12628000-12629000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr9:12628000-12629000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr9:12628800-12630000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr9:12628800-12630200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr9:12629000-12630000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr9:12629000-12630000	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr9:12629000-12630200	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr9:12629000-12630400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr9:12629000-12630600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr9:12629000-12631000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr9:12629000-12631000	Enhancers	HUES6 Cell Line	embryonic stem cell

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