Variant report

Variant	nsv498066
Chromosome Location	chr9:8961722-9486652
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	chr9:9054602-9054923	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:8961022-8961768	HepG2	liver:	n/a	n/a
3	BATF	chr9:9442020-9442372	GM12878	blood:	n/a	n/a
4	BCL11A	chr9:9442026-9442309	GM12878	blood:	n/a	n/a
5	BCL11A	chr9:9442015-9442337	GM12878	blood:	n/a	n/a
6	BHLHE40	chr9:9442013-9442278	HepG2	liver:	n/a	n/a
7	CEBPB	chr9:9378401-9378621	HepG2	liver:	n/a	chr9:9378542-9378553
8	CEBPB	chr9:9400061-9400321	HepG2	liver:	n/a	chr9:9400176-9400187 chr9:9400178-9400189
9	CEBPB	chr9:9010710-9011045	IMR90	lung:	n/a	chr9:9010892-9010905 chr9:9010894-9010903 chr9:9010892-9010903
10	CEBPB	chr9:9340162-9340258	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr9:9014250-9014489	HepG2	liver:	n/a	n/a
12	CEBPB	chr9:9226707-9226943	A549	lung:	n/a	chr9:9226847-9226860 chr9:9226849-9226860 chr9:9226847-9226858
13	CEBPB	chr9:9010854-9010971	H1-hESC	embryonic stem cell:	n/a	chr9:9010892-9010905 chr9:9010894-9010903 chr9:9010892-9010903
14	CEBPB	chr9:9162739-9163039	A549	lung:	n/a	n/a
15	CEBPB	chr9:8992944-8993144	HepG2	liver:	n/a	n/a
16	CEBPB	chr9:9010826-9010992	K562	blood:	n/a	chr9:9010892-9010905 chr9:9010894-9010903 chr9:9010892-9010903
17	CEBPB	chr9:9184918-9185156	H1-hESC	embryonic stem cell:	n/a	chr9:9185056-9185069 chr9:9185058-9185069 chr9:9185058-9185067 chr9:9184998-9185011 chr9:9185056-9185067
18	CEBPB	chr9:9226688-9226885	K562	blood:	n/a	chr9:9226847-9226860 chr9:9226849-9226860 chr9:9226847-9226858
19	CEBPB	chr9:9010741-9010996	A549	lung:	n/a	chr9:9010892-9010905 chr9:9010894-9010903 chr9:9010892-9010903
20	CEBPB	chr9:9414945-9415249	HepG2	liver:	n/a	chr9:9415076-9415087 chr9:9415078-9415087
21	CEBPB	chr9:8987639-8987844	H1-hESC	embryonic stem cell:	n/a	chr9:8987749-8987758 chr9:8987747-8987758 chr9:8987747-8987760
22	CEBPB	chr9:9050461-9050785	A549	lung:	n/a	chr9:9050601-9050612 chr9:9050622-9050633
23	CEBPB	chr9:9412259-9412459	H1-hESC	embryonic stem cell:	n/a	chr9:9412345-9412356
24	CEBPB	chr9:9219422-9219423	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr9:9050446-9050796	HepG2	liver:	n/a	chr9:9050601-9050612 chr9:9050622-9050633
26	CEBPB	chr9:9014242-9014411	IMR90	lung:	n/a	n/a
27	CEBPB	chr9:9214265-9214465	HepG2	liver:	n/a	chr9:9214334-9214345
28	CEBPB	chr9:9069738-9070034	HepG2	liver:	n/a	chr9:9069872-9069881
29	CEBPB	chr9:9097309-9097586	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr9:9162728-9163029	HepG2	liver:	n/a	n/a
31	CEBPB	chr9:9479287-9479475	HepG2	liver:	n/a	chr9:9479420-9479431
32	CEBPB	chr9:9191327-9191565	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:9177847-9178081	A549	lung:	n/a	chr9:9177988-9177999
34	CEBPB	chr9:8961081-8961810	HepG2	liver:	n/a	n/a
35	CEBPB	chr9:9416749-9417000	HepG2	liver:	n/a	chr9:9416870-9416881 chr9:9416868-9416879
36	CEBPB	chr9:9184906-9185209	HepG2	liver:	n/a	chr9:9185056-9185069 chr9:9185058-9185069 chr9:9185058-9185067 chr9:9184998-9185011 chr9:9185056-9185067
37	CEBPB	chr9:9069789-9070000	IMR90	lung:	n/a	chr9:9069872-9069881
38	CEBPB	chr9:9177863-9178135	HepG2	liver:	n/a	chr9:9177988-9177999
39	CEBPB	chr9:9378415-9378701	A549	lung:	n/a	chr9:9378542-9378553
40	CEBPB	chr9:9010715-9011060	HepG2	liver:	n/a	chr9:9010892-9010905 chr9:9010894-9010903 chr9:9010892-9010903
41	CEBPB	chr9:9255418-9255716	HepG2	liver:	n/a	n/a
42	CEBPB	chr9:9162739-9163026	IMR90	lung:	n/a	n/a
43	CEBPB	chr9:9050578-9050640	H1-hESC	embryonic stem cell:	n/a	chr9:9050601-9050612 chr9:9050622-9050633
44	CEBPB	chr9:9162786-9162996	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr9:9006505-9006741	HepG2	liver:	n/a	n/a
46	CEBPB	chr9:9054670-9055043	HepG2	liver:	n/a	chr9:9054827-9054838 chr9:9054861-9054872
47	CEBPB	chr9:8990077-8990402	HepG2	liver:	n/a	chr9:8990232-8990245 chr9:8990232-8990243
48	CEBPB	chr9:9293996-9294301	A549	lung:	n/a	chr9:9294176-9294187
49	CEBPB	chr9:9443446-9443672	HepG2	liver:	n/a	n/a
50	CEBPB	chr9:8961184-8961759	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:9091180-9091230	PANC-1	pancreas:	n/a
2	chr9:9091180-9091230	LNCaP	prostate:	n/a
3	chr9:9091180-9091230	Hepatocyte	liver:	n/a
4	chr9:9091180-9091230	AG09309	skin:	n/a
5	chr9:9091180-9091230	HIPEpiC	eye:	n/a
6	chr9:9091180-9091230	GM12891	blood:	n/a
7	chr9:9091180-9091230	SK-N-SH	brain:	n/a
8	chr9:9091180-9091230	AG04450	lung:	fetal
9	chr9:9091180-9091230	NT2-D1	testis:	n/a
10	chr9:9091180-9091230	PFSK-1	brain:	n/a
11	chr9:9091180-9091230	NHDF-neo	bronchial:	n/a
12	chr9:9091180-9091230	AG09319	gingival:	n/a
13	chr9:9091180-9091230	A549	lung:	n/a
14	chr9:9091180-9091230	HNPCEpiC	eye:	n/a
15	chr9:9091180-9091230	HRPEpiC	eye:	n/a
16	chr9:9091180-9091230	AG10803	skin:	n/a
17	chr9:9091180-9091230	SK-N-SH_RA	brain:	n/a
18	chr9:9091180-9091230	GM19239	blood:	n/a
19	chr9:9091180-9091230	NB4	blood:	n/a
20	chr9:9091180-9091230	MCF10A-Er-Src	breast:	n/a
21	chr9:9091180-9091230	HMEC	breast:	n/a
22	chr9:9091180-9091230	ProgFib	skin:	n/a
23	chr9:9091180-9091230	CMK	blood:	n/a
24	chr9:9091180-9091230	HCM	heart:	n/a
25	chr9:9091180-9091230	HRE	kidney:	n/a
26	chr9:9091180-9091230	HPAEpiC	pulmonary alveolar:	n/a
27	chr9:9091180-9091230	BE2_C	brain:	n/a
28	chr9:9091180-9091230	ECC-1	luminal epithelium:	n/a
29	chr9:9091180-9091230	HCT-116	colon:	n/a
30	chr9:9091180-9091230	Caco-2	colon:	n/a
31	chr9:9091180-9091230	Hela-S3	cervix:	n/a
32	chr9:9091180-9091230	IMR90	lung:	fetal
33	chr9:9091180-9091230	BJ	skin:	n/a
34	chr9:9091180-9091230	AG04449	skin:	fetal
35	chr9:9091180-9091230	HRCEpiC	kidney:	n/a
36	chr9:9091180-9091230	ovcar-3	ovarian:	n/a
37	chr9:9091180-9091230	HEK293	kidney:	embryo
38	chr9:9091180-9091230	RPTEC	kidney:	n/a
39	chr9:9091180-9091230	NH-A	brain:	n/a
40	chr9:9091180-9091230	SAEC	small airway:	n/a
41	chr9:9091180-9091230	GM12878	blood:	n/a
42	chr9:9091180-9091230	MCF-7	breast:	n/a
43	chr9:9091180-9091230	K562	blood:	n/a
44	chr9:9091180-9091230	HCPEpiC	choroid plexus:	n/a
45	chr9:9091180-9091230	GM06990	blood:	n/a
46	chr9:9091180-9091230	AoSMC	blood vessel:	n/a
47	chr9:9091180-9091230	HCF	heart:	n/a
48	chr9:9091180-9091230	HL-60	blood:	n/a
49	chr9:9091180-9091230	T-47D	breast:	n/a
50	chr9:9091180-9091230	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:56435690..56436195-chr9:9090395..9091395,2	HCT-116	colon:
2	chr12:56435752..56436286-chr9:9090373..9090875,2	MCF-7	breast:
3	chr9:9128289..9130655-chr9:9131606..9133901,2	K562	blood:
4	chr12:56435572..56436393-chr9:9090873..9091393,3	MCF-7	breast:
5	chr9:9353280..9355692-chr9:9355746..9358583,2	K562	blood:
6	chr12:56434264..56436145-chr9:9090873..9092394,2	K562	blood:
7	chr9:9128289..9130655-chr9:9131606..9133901,2	K562	blood:
8	chr9:9179702..9181500-chr9:9182795..9185230,2	K562	blood:
9	chr9:9353280..9355692-chr9:9355746..9358583,2	K562	blood:
10	chr9:9179702..9181500-chr9:9182795..9185230,2	K562	blood:
11	chr12:56434645..56437118-chr9:9089375..9092373,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM4C-9	chr9:8962800-8963077	ENSG00000234021
2	lnc-KDM4C-9	chr9:8962124-8962189	ENSG00000234021

Variant related genes	Relation type
RPS26P3	TF binding region
ENSG00000221708	TF binding region
RN7SL5P	TF binding region
RPS26P3	CpG island
ENSG00000221708	CpG island
RN7SL5P	CpG island
ENSG00000257449	chromatin interactions
ENSG00000197728	chromatin interactions

Extended variants
information (count: 9032 )
Associated
traits (count: 130 )

Variant overlapped rSNPs/rCNVs (count:9032 , 50 per page) page: 1 2 3 4 5 6 7 ... 181

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573155799	chr9:8961866-8961867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372692758	chr9:8961877-8961878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558570444	chr9:8961891-8961892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183797560	chr9:8961941-8961942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188171505	chr9:8961984-8961985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77073771	chr9:8962005-8962006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529866280	chr9:8962014-8962015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541959771	chr9:8962086-8962087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576698370	chr9:8962087-8962088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560467417	chr9:8962101-8962102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527625110	chr9:8962119-8962120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552496015	chr9:8962121-8962122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570489642	chr9:8962130-8962131	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs531321165	chr9:8962134-8962135	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs180708372	chr9:8962159-8962160	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs568119268	chr9:8962169-8962170	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs150568817	chr9:8962171-8962172	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs139586817	chr9:8962197-8962198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534340835	chr9:8962205-8962206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144306450	chr9:8962207-8962208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534269084	chr9:8962220-8962221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558806331	chr9:8962243-8962244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576863703	chr9:8962254-8962255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544564426	chr9:8962260-8962261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542500561	chr9:8962265-8962266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs41281791	chr9:8962271-8962272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574834052	chr9:8962296-8962297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs41281793	chr9:8962316-8962317	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs375982566	chr9:8962349-8962350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146533502	chr9:8962379-8962380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536199569	chr9:8962390-8962391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546153629	chr9:8962420-8962421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564339544	chr9:8962443-8962444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141216282	chr9:8962453-8962454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190534192	chr9:8962469-8962470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143631641	chr9:8962482-8962483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529026238	chr9:8962489-8962490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200206780	chr9:8962538-8962539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373367865	chr9:8962539-8962540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144308037	chr9:8962540-8962541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372601641	chr9:8962542-8962543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564689853	chr9:8962551-8962552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547089730	chr9:8962552-8962553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566754285	chr9:8962553-8962554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs397713112	chr9:8962556-8962557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534114816	chr9:8962557-8962558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368386154	chr9:8962585-8962586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372602031	chr9:8962598-8962599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552470686	chr9:8962603-8962604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370667352	chr9:8962604-8962605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:130)

Disease	PMID	Source
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	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
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
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	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
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	20668451	CNVD
Schizophrenia	20838587	CNVD
Glioblastoma	18772890	CNVD
Glioblastoma multiforme	21390271	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute myeloid leukemia	21251322	CNVD
Chordoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Autism	20531469	CNVD
Lung adenocarcinoma	17982442	CNVD

Chromatin state (count:464 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8957600-8962200	Enhancers	Liver	Liver
2	chr9:8958000-8962600	Enhancers	HepG2	liver
3	chr9:8959800-8962000	Enhancers	Adipose Nuclei	Adipose
4	chr9:8960000-8962000	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr9:8960200-8962600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:8960200-8963200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:8960400-8962600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr9:8960600-8961800	Enhancers	Fetal Heart	heart
9	chr9:8961200-8961800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr9:8961200-8961800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr9:8961200-8961800	Enhancers	Brain Angular Gyrus	brain
12	chr9:8961200-8961800	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr9:8961200-8962000	Enhancers	Brain Cingulate Gyrus	brain
14	chr9:8961400-8961800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr9:8961400-8961800	Enhancers	Right Atrium	heart
16	chr9:8961400-8961800	Enhancers	Dnd41	blood
17	chr9:8961800-8966200	Weak transcription	Dnd41	blood
18	chr9:8962000-8963600	Weak transcription	Adipose Nuclei	Adipose
19	chr9:8962600-8963600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr9:8963200-8963400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr9:8963400-8963600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr9:8963600-8964000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:8963600-8964000	Enhancers	Adipose Nuclei	Adipose
24	chr9:8963600-8964000	Enhancers	Ovary	ovary
25	chr9:8963600-8964600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr9:8964000-8964800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr9:8966200-8967600	Enhancers	Dnd41	blood
28	chr9:8967600-8968600	Weak transcription	Dnd41	blood
29	chr9:8968600-8970000	Enhancers	Dnd41	blood
30	chr9:8980600-8981200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr9:8980600-8982000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr9:8987200-8987600	Enhancers	H9 Cell Line	embryonic stem cell
33	chr9:8987200-8987600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr9:8987200-8987600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr9:8987200-8987800	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr9:8987200-8988000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr9:8987400-8987800	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr9:8987400-8988000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr9:8996200-8996800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr9:9000000-9000200	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr9:9000200-9000800	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr9:9000800-9001800	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr9:9002600-9002800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr9:9002600-9005400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr9:9002800-9003200	Enhancers	Liver	Liver
46	chr9:9002800-9003400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr9:9002800-9003400	Enhancers	Aorta	Aorta
48	chr9:9002800-9004000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr9:9003000-9003200	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr9:9003000-9003800	Enhancers	Brain Cingulate Gyrus	brain

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