Variant report

Variant	nsv613702
Chromosome Location	chr9:17583310-17630591
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	BRCA1	chr9:17615714-17616232	Hela-S3	cervix:	n/a	n/a
2	BRCA1	chr9:17614932-17615321	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr9:17630356-17631147	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr9:17627759-17628044	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr9:17614983-17615236	MCF-7	breast:	n/a	chr9:17615138-17615149
6	CEBPB	chr9:17615004-17615229	A549	lung:	n/a	chr9:17615138-17615149
7	CEBPB	chr9:17629978-17632015	Hela-S3	cervix:	n/a	chr9:17630738-17630751 chr9:17631912-17631925 chr9:17631558-17631566 chr9:17630738-17630749
8	CEBPB	chr9:17607328-17607618	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr9:17628638-17629066	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr9:17587199-17587501	HepG2	liver:	n/a	chr9:17587326-17587337
11	CEBPB	chr9:17623974-17624320	Hela-S3	cervix:	n/a	chr9:17624148-17624159
12	CEBPB	chr9:17615547-17615651	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr9:17630514-17630924	ECC-1	luminal epithelium:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
14	CEBPB	chr9:17614954-17615307	HepG2	liver:	n/a	chr9:17615138-17615149
15	CEBPB	chr9:17630429-17631023	ECC-1	luminal epithelium:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
16	CEBPB	chr9:17614965-17615325	ECC-1	luminal epithelium:	n/a	chr9:17615138-17615149
17	CEBPB	chr9:17594289-17594350	HepG2	liver:	n/a	n/a
18	CEBPB	chr9:17592528-17592868	HepG2	liver:	n/a	chr9:17592694-17592705
19	CEBPB	chr9:17627674-17628045	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:17592526-17592860	A549	lung:	n/a	chr9:17592694-17592705
21	CEBPB	chr9:17592528-17592872	IMR90	lung:	n/a	chr9:17592694-17592705
22	CEBPB	chr9:17625646-17626018	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr9:17614857-17615380	ECC-1	luminal epithelium:	n/a	chr9:17615138-17615149
24	CEBPB	chr9:17587171-17587497	H1-hESC	embryonic stem cell:	n/a	chr9:17587326-17587337
25	CEBPB	chr9:17587205-17587469	Hela-S3	cervix:	n/a	chr9:17587326-17587337
26	CEBPB	chr9:17614997-17615244	H1-hESC	embryonic stem cell:	n/a	chr9:17615138-17615149
27	CEBPB	chr9:17623986-17624320	IMR90	lung:	n/a	chr9:17624148-17624159
28	CEBPB	chr9:17587142-17587477	ECC-1	luminal epithelium:	n/a	chr9:17587326-17587337
29	CEBPB	chr9:17613398-17614137	Hela-S3	cervix:	n/a	chr9:17613504-17613516
30	CEBPB	chr9:17584689-17584710	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr9:17614980-17615315	IMR90	lung:	n/a	chr9:17615138-17615149
32	CEBPB	chr9:17587172-17587471	A549	lung:	n/a	chr9:17587326-17587337
33	CEBPB	chr9:17614739-17615763	Hela-S3	cervix:	n/a	chr9:17615138-17615149
34	CEBPB	chr9:17623976-17624330	HepG2	liver:	n/a	chr9:17624148-17624159
35	CEBPB	chr9:17623982-17624335	A549	lung:	n/a	chr9:17624148-17624159
36	CHD2	chr9:17625614-17625983	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr9:17627701-17628040	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr9:17614881-17615285	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr9:17630387-17631090	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr9:17598560-17598710	NB4	blood:	n/a	n/a
41	CTCF	chr9:17587220-17587370	BE2_C	brain:	n/a	n/a
42	CTCF	chr9:17622400-17622550	RPTEC	kidney:	n/a	n/a
43	CTCF	chr9:17615089-17615258	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr9:17588700-17588850	NHEK	skin:	n/a	n/a
45	CTCF	chr9:17593261-17593310	ProgFib	skin:	n/a	n/a
46	CTCF	chr9:17587320-17587470	HCT-116	colon:	n/a	n/a
47	CTCF	chr9:17587239-17587377	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr9:17622500-17622650	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr9:17587279-17587318	Gliobla	brain:	n/a	n/a
50	CTCF	chr9:17586840-17586990	GM12865	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17591842-17591892	SK-N-MC	brain:	n/a
2	chr9:17591842-17591892	SK-N-MC	brain:	n/a
3	chr9:17591842-17591892	AG10803	skin:	n/a
4	chr9:17591842-17591892	ProgFib	skin:	n/a
5	chr9:17591842-17591892	A549	lung:	n/a
6	chr9:17591842-17591892	U87	brain:	n/a
7	chr9:17591842-17591892	MCF10A-Er-Src	breast:	n/a
8	chr9:17591842-17591892	HPAEpiC	pulmonary alveolar:	n/a
9	chr9:17591842-17591892	PFSK-1	brain:	n/a
10	chr9:17591842-17591892	HepG2	liver:	n/a
11	chr9:17591842-17591892	HAEpiC	amniotic membrane:	n/a
12	chr9:17591842-17591892	ECC-1	luminal epithelium:	n/a
13	chr9:17591842-17591892	CMK	blood:	n/a
14	chr9:17591842-17591892	ovcar-3	ovarian:	n/a
15	chr9:17591842-17591892	AoSMC	blood vessel:	n/a
16	chr9:17591842-17591892	HRE	kidney:	n/a
17	chr9:17591842-17591892	Hela-S3	cervix:	n/a
18	chr9:17591842-17591892	HNPCEpiC	eye:	n/a
19	chr9:17591842-17591892	NH-A	brain:	n/a
20	chr9:17591842-17591892	PANC-1	pancreas:	n/a
21	chr9:17591842-17591892	HRPEpiC	eye:	n/a
22	chr9:17591842-17591892	AG04449	skin:	fetal
23	chr9:17591842-17591892	BJ	skin:	n/a
24	chr9:17591842-17591892	HCM	heart:	n/a
25	chr9:17591842-17591892	Jurkat	blood:	n/a
26	chr9:17591842-17591892	NB4	blood:	n/a
27	chr9:17591842-17591892	H1-hESC	embryonic stem cell:	embryo
28	chr9:17591842-17591892	PrEC	prostate:	n/a
29	chr9:17591842-17591892	GM12891	blood:	n/a
30	chr9:17591842-17591892	GM19239	blood:	n/a
31	chr9:17591842-17591892	AG04450	lung:	fetal
32	chr9:17591842-17591892	LNCaP	prostate:	n/a
33	chr9:17591842-17591892	HMEC	breast:	n/a
34	chr9:17591842-17591892	SAEC	small airway:	n/a
35	chr9:17591842-17591892	HCPEpiC	choroid plexus:	n/a
36	chr9:17591842-17591892	BE2_C	brain:	n/a
37	chr9:17591842-17591892	HEK293	kidney:	embryo
38	chr9:17591842-17591892	HCF	heart:	n/a
39	chr9:17591842-17591892	K562	blood:	n/a
40	chr9:17591842-17591892	HIPEpiC	eye:	n/a
41	chr9:17591842-17591892	HCT-116	colon:	n/a
42	chr9:17591842-17591892	GM06990	blood:	n/a
43	chr9:17591842-17591892	RPTEC	kidney:	n/a
44	chr9:17591842-17591892	NT2-D1	testis:	n/a
45	chr9:17591842-17591892	SK-N-SH_RA	brain:	n/a
46	chr9:17591842-17591892	T-47D	breast:	n/a
47	chr9:17591842-17591892	NHBE	bronchial:	n/a
48	chr9:17591842-17591892	HRCEpiC	kidney:	n/a
49	chr9:17591842-17591892	MCF-7	breast:	n/a
50	chr9:17591842-17591892	IMR90	lung:	fetal

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTLN-5	chr9:17630352-17630427	NONHSAT130304
2	lnc-BNC2-5	chr9:17590903-17591316	NONHSAT130305
3	lnc-BNC2-5	chr9:17589159-17590751	NONHSAT130305

Variant related genes	Relation type
PABPC1P11	TF binding region
PABPC1P11	CpG island

Extended variants
information (count: 2353 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2353 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1028594	chr9:17583310-17583311	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550075097	chr9:17583334-17583335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146993248	chr9:17583351-17583352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181008167	chr9:17583398-17583399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532651517	chr9:17583426-17583427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547732288	chr9:17583437-17583438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183843715	chr9:17583498-17583499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78169069	chr9:17583500-17583501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566114720	chr9:17583551-17583552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374933934	chr9:17583578-17583579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528996795	chr9:17583648-17583649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189658946	chr9:17583709-17583710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533567998	chr9:17583711-17583712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552202593	chr9:17583757-17583758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548588124	chr9:17583791-17583792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs10120378	chr9:17583846-17583847	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs537956044	chr9:17583872-17583873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553211530	chr9:17583888-17583889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574939950	chr9:17583951-17583952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556037513	chr9:17583971-17583972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535679289	chr9:17583972-17583973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs137993102	chr9:17583973-17583974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576054228	chr9:17583998-17583999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181643947	chr9:17584018-17584019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545805737	chr9:17584037-17584038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564105094	chr9:17584045-17584046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572954009	chr9:17584049-17584050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142036367	chr9:17584098-17584099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186680654	chr9:17584100-17584101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150118479	chr9:17584149-17584150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191982335	chr9:17584201-17584202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562801377	chr9:17584222-17584223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10810811	chr9:17584225-17584226	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs552128644	chr9:17584269-17584270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10756891	chr9:17584274-17584275	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs528480239	chr9:17584302-17584303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368933432	chr9:17584345-17584346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181913002	chr9:17584375-17584376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113495098	chr9:17584456-17584457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7028060	chr9:17584457-17584458	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs536043214	chr9:17584458-17584459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373486056	chr9:17584484-17584485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373387712	chr9:17584504-17584505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557313185	chr9:17584510-17584511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144389817	chr9:17584548-17584549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139037269	chr9:17584553-17584554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537276936	chr9:17584558-17584559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558511685	chr9:17584611-17584612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186560095	chr9:17584663-17584664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539859029	chr9:17584681-17584682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
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
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	21364760	CNVD
Cancer	22183965	CNVD
Lung adenocarcinoma	21935476	CNVD
Thoracic aortic aneurysm	21698135	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17580800-17589600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr9:17581000-17583600	Weak transcription	Brain Angular Gyrus	brain
3	chr9:17581400-17590000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr9:17582000-17584600	Weak transcription	Fetal Brain Female	brain
5	chr9:17583000-17584000	Weak transcription	Fetal Brain Male	brain
6	chr9:17583200-17583800	Enhancers	Hela-S3	cervix
7	chr9:17584600-17585800	Enhancers	Fetal Brain Female	brain
8	chr9:17585600-17585800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:17585600-17585800	Enhancers	Fetal Brain Male	brain
10	chr9:17585800-17589600	Weak transcription	Fetal Brain Female	brain
11	chr9:17587200-17587400	Enhancers	H1 Cell Line	embryonic stem cell
12	chr9:17588400-17588600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr9:17589600-17589800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
14	chr9:17589600-17590000	Enhancers	Fetal Brain Female	brain
15	chr9:17589800-17590000	Enhancers	Gastric	stomach
16	chr9:17590000-17590600	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr9:17590600-17600400	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr9:17591600-17592000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr9:17591600-17592400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr9:17591600-17592800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr9:17591600-17593000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr9:17591800-17592400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:17591800-17592600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr9:17591800-17592600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr9:17591800-17592800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr9:17592000-17592400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr9:17592000-17593000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr9:17595200-17595400	Enhancers	Dnd41	blood
29	chr9:17598000-17598200	Enhancers	Psoas Muscle	Psoas
30	chr9:17599200-17599600	Enhancers	Fetal Brain Female	brain
31	chr9:17599400-17599600	Enhancers	Hela-S3	cervix
32	chr9:17599600-17600600	Weak transcription	Hela-S3	cervix
33	chr9:17599800-17600600	Weak transcription	Fetal Heart	heart
34	chr9:17600400-17601200	Enhancers	Fetal Brain Male	brain
35	chr9:17600400-17602200	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr9:17600600-17600800	Enhancers	Fetal Heart	heart
37	chr9:17600600-17602000	Enhancers	Hela-S3	cervix
38	chr9:17600800-17601800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr9:17600800-17607400	Weak transcription	Fetal Heart	heart
40	chr9:17601000-17601600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr9:17601000-17601800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr9:17601000-17601800	Enhancers	NH-A	brain
43	chr9:17602000-17604000	Weak transcription	Hela-S3	cervix
44	chr9:17602200-17608600	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr9:17604000-17605000	Enhancers	Hela-S3	cervix
46	chr9:17605000-17608600	Weak transcription	Hela-S3	cervix
47	chr9:17607400-17613000	Enhancers	Fetal Heart	heart
48	chr9:17608600-17608800	Enhancers	Hela-S3	cervix
49	chr9:17608600-17610800	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr9:17608800-17609200	Weak transcription	Hela-S3	cervix

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