Variant report

Variant	nsv1031193
Chromosome Location	chr9:17590299-17636674
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	chr9:17630356-17631147	Hela-S3	cervix:	n/a	n/a
2	BRCA1	chr9:17627759-17628044	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr9:17614932-17615321	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr9:17615714-17616232	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr9:17594289-17594350	HepG2	liver:	n/a	n/a
6	CEBPB	chr9:17614983-17615236	MCF-7	breast:	n/a	chr9:17615138-17615149
7	CEBPB	chr9:17623986-17624320	IMR90	lung:	n/a	chr9:17624148-17624159
8	CEBPB	chr9:17615547-17615651	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr9:17592528-17592868	HepG2	liver:	n/a	chr9:17592694-17592705
10	CEBPB	chr9:17615004-17615229	A549	lung:	n/a	chr9:17615138-17615149
11	CEBPB	chr9:17630600-17630833	H1-hESC	embryonic stem cell:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
12	CEBPB	chr9:17623982-17624335	A549	lung:	n/a	chr9:17624148-17624159
13	CEBPB	chr9:17614857-17615380	ECC-1	luminal epithelium:	n/a	chr9:17615138-17615149
14	CEBPB	chr9:17592528-17592872	IMR90	lung:	n/a	chr9:17592694-17592705
15	CEBPB	chr9:17628638-17629066	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr9:17614965-17615325	ECC-1	luminal epithelium:	n/a	chr9:17615138-17615149
17	CEBPB	chr9:17592526-17592860	A549	lung:	n/a	chr9:17592694-17592705
18	CEBPB	chr9:17614739-17615763	Hela-S3	cervix:	n/a	chr9:17615138-17615149
19	CEBPB	chr9:17629978-17632015	Hela-S3	cervix:	n/a	chr9:17630738-17630751 chr9:17631912-17631925 chr9:17631558-17631566 chr9:17630738-17630749
20	CEBPB	chr9:17607328-17607618	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr9:17634991-17635180	A549	lung:	n/a	n/a
22	CEBPB	chr9:17634897-17635195	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr9:17636332-17636742	Hela-S3	cervix:	n/a	chr9:17636377-17636389
24	CEBPB	chr9:17614954-17615307	HepG2	liver:	n/a	chr9:17615138-17615149
25	CEBPB	chr9:17614997-17615244	H1-hESC	embryonic stem cell:	n/a	chr9:17615138-17615149
26	CEBPB	chr9:17623974-17624320	Hela-S3	cervix:	n/a	chr9:17624148-17624159
27	CEBPB	chr9:17623976-17624330	HepG2	liver:	n/a	chr9:17624148-17624159
28	CEBPB	chr9:17630429-17631023	ECC-1	luminal epithelium:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
29	CEBPB	chr9:17625646-17626018	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr9:17630514-17630924	ECC-1	luminal epithelium:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
31	CEBPB	chr9:17614980-17615315	IMR90	lung:	n/a	chr9:17615138-17615149
32	CEBPB	chr9:17627674-17628045	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr9:17613398-17614137	Hela-S3	cervix:	n/a	chr9:17613504-17613516
34	CEBPB	chr9:17633008-17633404	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr9:17627701-17628040	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr9:17625614-17625983	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr9:17630387-17631090	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr9:17614881-17615285	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr9:17622460-17622610	HAc	cerebellar:	n/a	n/a
40	CTCF	chr9:17622500-17622650	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr9:17622456-17622579	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr9:17609660-17609810	BJ	skin:	n/a	n/a
43	CTCF	chr9:17622440-17622590	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr9:17622400-17622550	RPTEC	kidney:	n/a	n/a
45	CTCF	chr9:17622400-17622550	GM06990	blood:	n/a	n/a
46	CTCF	chr9:17622380-17622530	HEK293	kidney:	n/a	n/a
47	CTCF	chr9:17598560-17598710	NB4	blood:	n/a	n/a
48	CTCF	chr9:17604029-17604034	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr9:17622220-17622370	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr9:17615089-17615258	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17591842-17591892	Caco-2	colon:	n/a
2	chr9:17591842-17591892	K562	blood:	n/a
3	chr9:17591842-17591892	HCPEpiC	choroid plexus:	n/a
4	chr9:17591842-17591892	PFSK-1	brain:	n/a
5	chr9:17591842-17591892	Hepatocyte	liver:	n/a
6	chr9:17591842-17591892	HRPEpiC	eye:	n/a
7	chr9:17591842-17591892	SK-N-MC	brain:	n/a
8	chr9:17591842-17591892	SKMC	muscle:	n/a
9	chr9:17591842-17591892	LNCaP	prostate:	n/a
10	chr9:17591842-17591892	HRE	kidney:	n/a
11	chr9:17591842-17591892	GM19239	blood:	n/a
12	chr9:17591842-17591892	HAEpiC	amniotic membrane:	n/a
13	chr9:17591842-17591892	AG09309	skin:	n/a
14	chr9:17591842-17591892	GM06990	blood:	n/a
15	chr9:17591842-17591892	NH-A	brain:	n/a
16	chr9:17591842-17591892	HCT-116	colon:	n/a
17	chr9:17591842-17591892	U87	brain:	n/a
18	chr9:17591842-17591892	ovcar-3	ovarian:	n/a
19	chr9:17591842-17591892	HCF	heart:	n/a
20	chr9:17591842-17591892	PrEC	prostate:	n/a
21	chr9:17591842-17591892	PANC-1	pancreas:	n/a
22	chr9:17591842-17591892	HIPEpiC	eye:	n/a
23	chr9:17591842-17591892	ProgFib	skin:	n/a
24	chr9:17591842-17591892	BJ	skin:	n/a
25	chr9:17591842-17591892	H1-hESC	embryonic stem cell:	embryo
26	chr9:17591842-17591892	HNPCEpiC	eye:	n/a
27	chr9:17591842-17591892	AG04449	skin:	fetal
28	chr9:17591842-17591892	ECC-1	luminal epithelium:	n/a
29	chr9:17591842-17591892	HUVEC	blood vessel:	n/a
30	chr9:17591842-17591892	MCF10A-Er-Src	breast:	n/a
31	chr9:17591842-17591892	HEEpiC	esophagus:	n/a
32	chr9:17591842-17591892	HEK293	kidney:	embryo
33	chr9:17591842-17591892	HRCEpiC	kidney:	n/a
34	chr9:17591842-17591892	AoSMC	blood vessel:	n/a
35	chr9:17591842-17591892	SK-N-SH_RA	brain:	n/a
36	chr9:17591842-17591892	GM12891	blood:	n/a
37	chr9:17591842-17591892	NT2-D1	testis:	n/a
38	chr9:17591842-17591892	IMR90	lung:	fetal
39	chr9:17591842-17591892	HL-60	blood:	n/a
40	chr9:17591842-17591892	SK-N-SH	brain:	n/a
41	chr9:17591842-17591892	RPTEC	kidney:	n/a
42	chr9:17591842-17591892	Jurkat	blood:	n/a
43	chr9:17591842-17591892	Hela-S3	cervix:	n/a
44	chr9:17591842-17591892	BE2_C	brain:	n/a
45	chr9:17591842-17591892	HCM	heart:	n/a
46	chr9:17591842-17591892	NHBE	bronchial:	n/a
47	chr9:17591842-17591892	SAEC	small airway:	n/a
48	chr9:17591842-17591892	GM12892	blood:	n/a
49	chr9:17591842-17591892	HMEC	breast:	n/a
50	chr9:17591842-17591892	HepG2	liver:	n/a

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

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

Extended variants
information (count: 2364 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2364 , 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	rs3808776	chr9:17590299-17590300	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555125540	chr9:17590350-17590351	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs139155532	chr9:17590374-17590375	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs73641993	chr9:17590431-17590432	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs144019219	chr9:17590467-17590468	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs71504865	chr9:17590481-17590482	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs116051359	chr9:17590525-17590526	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs146454012	chr9:17590607-17590608	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs560400003	chr9:17590648-17590649	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs182906900	chr9:17590656-17590657	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs144737533	chr9:17590666-17590667	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs543371864	chr9:17590739-17590740	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs540662680	chr9:17590744-17590745	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs187584915	chr9:17590774-17590775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544788650	chr9:17590786-17590787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114867871	chr9:17590787-17590788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370841989	chr9:17590791-17590792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544804143	chr9:17590806-17590807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563035651	chr9:17590813-17590814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533587696	chr9:17590820-17590821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192423781	chr9:17590840-17590841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567159954	chr9:17590843-17590844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564737759	chr9:17590869-17590870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185790595	chr9:17590903-17590904	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs548993749	chr9:17590905-17590906	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs373599802	chr9:17590912-17590913	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs567009972	chr9:17590926-17590927	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs578209648	chr9:17590946-17590947	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs545132749	chr9:17590947-17590948	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs144625840	chr9:17590963-17590964	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs373212656	chr9:17590964-17590965	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs532200861	chr9:17590981-17590982	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs555864631	chr9:17590982-17590983	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs377284796	chr9:17590984-17590985	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs146629865	chr9:17590991-17590992	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs538837314	chr9:17590994-17590995	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs553773245	chr9:17590998-17590999	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs369954443	chr9:17591024-17591025	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs572353465	chr9:17591035-17591036	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs112407690	chr9:17591042-17591043	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs547565462	chr9:17591043-17591044	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs555832454	chr9:17591045-17591046	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs187580200	chr9:17591046-17591047	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs368708944	chr9:17591047-17591048	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs540818745	chr9:17591048-17591049	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs562971659	chr9:17591077-17591078	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs113116786	chr9:17591157-17591158	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs545620412	chr9:17591169-17591170	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs560617539	chr9:17591192-17591193	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs143403128	chr9:17591204-17591205	Weak transcription	lncRNA	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:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17590000-17590600	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr9:17590600-17600400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr9:17591600-17592000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:17591600-17592400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr9:17591600-17592800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr9:17591600-17593000	Enhancers	H1 Cell Line	embryonic stem cell
7	chr9:17591800-17592400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:17591800-17592600	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr9:17591800-17592600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr9:17591800-17592800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr9:17592000-17592400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr9:17592000-17593000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr9:17595200-17595400	Enhancers	Dnd41	blood
14	chr9:17598000-17598200	Enhancers	Psoas Muscle	Psoas
15	chr9:17599200-17599600	Enhancers	Fetal Brain Female	brain
16	chr9:17599400-17599600	Enhancers	Hela-S3	cervix
17	chr9:17599600-17600600	Weak transcription	Hela-S3	cervix
18	chr9:17599800-17600600	Weak transcription	Fetal Heart	heart
19	chr9:17600400-17601200	Enhancers	Fetal Brain Male	brain
20	chr9:17600400-17602200	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr9:17600600-17600800	Enhancers	Fetal Heart	heart
22	chr9:17600600-17602000	Enhancers	Hela-S3	cervix
23	chr9:17600800-17601800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr9:17600800-17607400	Weak transcription	Fetal Heart	heart
25	chr9:17601000-17601600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr9:17601000-17601800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr9:17601000-17601800	Enhancers	NH-A	brain
28	chr9:17602000-17604000	Weak transcription	Hela-S3	cervix
29	chr9:17602200-17608600	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr9:17604000-17605000	Enhancers	Hela-S3	cervix
31	chr9:17605000-17608600	Weak transcription	Hela-S3	cervix
32	chr9:17607400-17613000	Enhancers	Fetal Heart	heart
33	chr9:17608600-17608800	Enhancers	Hela-S3	cervix
34	chr9:17608600-17610800	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr9:17608800-17609200	Weak transcription	Hela-S3	cervix
36	chr9:17609000-17609400	Enhancers	Left Ventricle	heart
37	chr9:17609200-17610000	Enhancers	Hela-S3	cervix
38	chr9:17609800-17610000	Enhancers	Left Ventricle	heart
39	chr9:17609800-17612400	Weak transcription	Fetal Brain Male	brain
40	chr9:17610000-17611400	Weak transcription	Hela-S3	cervix
41	chr9:17610800-17611800	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr9:17611400-17612000	Enhancers	Hela-S3	cervix
43	chr9:17611600-17612200	Enhancers	Left Ventricle	heart
44	chr9:17611800-17613600	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr9:17611800-17615200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr9:17612000-17612200	Enhancers	Brain Germinal Matrix	brain
47	chr9:17612000-17612400	Flanking Active TSS	Hela-S3	cervix
48	chr9:17612000-17615200	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr9:17612200-17613600	Weak transcription	Brain Germinal Matrix	brain
50	chr9:17612400-17612600	Enhancers	Brain Anterior Caudate	brain

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