Variant report

Variant	nsv1032604
Chromosome Location	chr9:17585687-17633296
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	chr9:17615714-17616232	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr9:17627759-17628044	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr9:17614932-17615321	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr9:17614954-17615307	HepG2	liver:	n/a	chr9:17615138-17615149
6	CEBPB	chr9:17629978-17632015	Hela-S3	cervix:	n/a	chr9:17630738-17630751 chr9:17631912-17631925 chr9:17631558-17631566 chr9:17630738-17630749
7	CEBPB	chr9:17614997-17615244	H1-hESC	embryonic stem cell:	n/a	chr9:17615138-17615149
8	CEBPB	chr9:17627674-17628045	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr9:17633008-17633404	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr9:17614965-17615325	ECC-1	luminal epithelium:	n/a	chr9:17615138-17615149
11	CEBPB	chr9:17615547-17615651	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr9:17592528-17592872	IMR90	lung:	n/a	chr9:17592694-17592705
13	CEBPB	chr9:17628638-17629066	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr9:17587205-17587469	Hela-S3	cervix:	n/a	chr9:17587326-17587337
15	CEBPB	chr9:17594289-17594350	HepG2	liver:	n/a	n/a
16	CEBPB	chr9:17614980-17615315	IMR90	lung:	n/a	chr9:17615138-17615149
17	CEBPB	chr9:17607328-17607618	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr9:17623974-17624320	Hela-S3	cervix:	n/a	chr9:17624148-17624159
19	CEBPB	chr9:17613398-17614137	Hela-S3	cervix:	n/a	chr9:17613504-17613516
20	CEBPB	chr9:17614739-17615763	Hela-S3	cervix:	n/a	chr9:17615138-17615149
21	CEBPB	chr9:17625646-17626018	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr9:17630600-17630833	H1-hESC	embryonic stem cell:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
23	CEBPB	chr9:17592528-17592868	HepG2	liver:	n/a	chr9:17592694-17592705
24	CEBPB	chr9:17623976-17624330	HepG2	liver:	n/a	chr9:17624148-17624159
25	CEBPB	chr9:17587172-17587471	A549	lung:	n/a	chr9:17587326-17587337
26	CEBPB	chr9:17587199-17587501	HepG2	liver:	n/a	chr9:17587326-17587337
27	CEBPB	chr9:17623986-17624320	IMR90	lung:	n/a	chr9:17624148-17624159
28	CEBPB	chr9:17630429-17631023	ECC-1	luminal epithelium:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
29	CEBPB	chr9:17587142-17587477	ECC-1	luminal epithelium:	n/a	chr9:17587326-17587337
30	CEBPB	chr9:17587171-17587497	H1-hESC	embryonic stem cell:	n/a	chr9:17587326-17587337
31	CEBPB	chr9:17614983-17615236	MCF-7	breast:	n/a	chr9:17615138-17615149
32	CEBPB	chr9:17592526-17592860	A549	lung:	n/a	chr9:17592694-17592705
33	CEBPB	chr9:17623982-17624335	A549	lung:	n/a	chr9:17624148-17624159
34	CEBPB	chr9:17630514-17630924	ECC-1	luminal epithelium:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
35	CEBPB	chr9:17614857-17615380	ECC-1	luminal epithelium:	n/a	chr9:17615138-17615149
36	CEBPB	chr9:17615004-17615229	A549	lung:	n/a	chr9:17615138-17615149
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	chr9:17625614-17625983	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr9:17630387-17631090	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr9:17587290-17587341	HepG2	liver:	n/a	n/a
42	CTCF	chr9:17604029-17604034	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr9:17587240-17587390	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr9:17587211-17587497	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr9:17622380-17622530	HEK293	kidney:	n/a	n/a
46	CTCF	chr9:17587320-17587470	HCT-116	colon:	n/a	n/a
47	CTCF	chr9:17622220-17622370	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr9:17609720-17609870	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr9:17622440-17622590	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr9:17587200-17587350	BJ	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17591842-17591892	A549	lung:	n/a
2	chr9:17591842-17591892	A549	lung:	n/a
3	chr9:17591842-17591892	HCPEpiC	choroid plexus:	n/a
4	chr9:17591842-17591892	GM12891	blood:	n/a
5	chr9:17591842-17591892	HCT-116	colon:	n/a
6	chr9:17591842-17591892	HepG2	liver:	n/a
7	chr9:17591842-17591892	T-47D	breast:	n/a
8	chr9:17591842-17591892	K562	blood:	n/a
9	chr9:17591842-17591892	NHDF-neo	bronchial:	n/a
10	chr9:17591842-17591892	CMK	blood:	n/a
11	chr9:17591842-17591892	SK-N-SH	brain:	n/a
12	chr9:17591842-17591892	BE2_C	brain:	n/a
13	chr9:17591842-17591892	MCF10A-Er-Src	breast:	n/a
14	chr9:17591842-17591892	HL-60	blood:	n/a
15	chr9:17591842-17591892	GM12892	blood:	n/a
16	chr9:17591842-17591892	GM19239	blood:	n/a
17	chr9:17591842-17591892	NB4	blood:	n/a
18	chr9:17591842-17591892	AoSMC	blood vessel:	n/a
19	chr9:17591842-17591892	AG09309	skin:	n/a
20	chr9:17591842-17591892	Jurkat	blood:	n/a
21	chr9:17591842-17591892	SK-N-MC	brain:	n/a
22	chr9:17591842-17591892	HNPCEpiC	eye:	n/a
23	chr9:17591842-17591892	HRE	kidney:	n/a
24	chr9:17591842-17591892	HEK293	kidney:	embryo
25	chr9:17591842-17591892	AG09319	gingival:	n/a
26	chr9:17591842-17591892	HRPEpiC	eye:	n/a
27	chr9:17591842-17591892	ovcar-3	ovarian:	n/a
28	chr9:17591842-17591892	HAEpiC	amniotic membrane:	n/a
29	chr9:17591842-17591892	RPTEC	kidney:	n/a
30	chr9:17591842-17591892	NT2-D1	testis:	n/a
31	chr9:17591842-17591892	SAEC	small airway:	n/a
32	chr9:17591842-17591892	AG04450	lung:	fetal
33	chr9:17591842-17591892	PFSK-1	brain:	n/a
34	chr9:17591842-17591892	Hela-S3	cervix:	n/a
35	chr9:17591842-17591892	SKMC	muscle:	n/a
36	chr9:17591842-17591892	MCF-7	breast:	n/a
37	chr9:17591842-17591892	ProgFib	skin:	n/a
38	chr9:17591842-17591892	HRCEpiC	kidney:	n/a
39	chr9:17591842-17591892	HCF	heart:	n/a
40	chr9:17591842-17591892	HMEC	breast:	n/a
41	chr9:17591842-17591892	NHBE	bronchial:	n/a
42	chr9:17591842-17591892	GM06990	blood:	n/a
43	chr9:17591842-17591892	GM12878	blood:	n/a
44	chr9:17591842-17591892	NH-A	brain:	n/a
45	chr9:17591842-17591892	H1-hESC	embryonic stem cell:	embryo
46	chr9:17591842-17591892	PrEC	prostate:	n/a
47	chr9:17591842-17591892	HUVEC	blood vessel:	n/a
48	chr9:17591842-17591892	PANC-1	pancreas:	n/a
49	chr9:17591842-17591892	IMR90	lung:	fetal
50	chr9:17591842-17591892	HCM	heart:	n/a

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: 2394 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2394 , 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	rs533520220	chr9:17585706-17585707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs75257360	chr9:17585720-17585721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567165247	chr9:17585752-17585753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534262144	chr9:17585759-17585760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549669087	chr9:17585767-17585768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567114014	chr9:17585815-17585816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537855839	chr9:17585823-17585824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75924204	chr9:17585826-17585827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577363808	chr9:17585880-17585881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7047611	chr9:17585896-17585897	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs7047709	chr9:17585919-17585920	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs114555019	chr9:17585973-17585974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115569501	chr9:17585985-17585986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373606006	chr9:17585986-17585987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183413291	chr9:17585989-17585990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573912248	chr9:17585991-17585992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544622192	chr9:17585999-17586000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562969563	chr9:17586004-17586005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188293957	chr9:17586015-17586016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs57007271	chr9:17586042-17586043	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs554032165	chr9:17586049-17586050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560554453	chr9:17586066-17586067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145610827	chr9:17586069-17586070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141470420	chr9:17586072-17586073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567950284	chr9:17586075-17586076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537438508	chr9:17586084-17586085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549405631	chr9:17586096-17586097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10810812	chr9:17586101-17586102	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs376579382	chr9:17586105-17586106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553472723	chr9:17586142-17586143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77125232	chr9:17586199-17586200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536449311	chr9:17586233-17586234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145310167	chr9:17586250-17586251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576324712	chr9:17586271-17586272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192294420	chr9:17586273-17586274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556620148	chr9:17586278-17586279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375996547	chr9:17586285-17586286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112808269	chr9:17586286-17586287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184678363	chr9:17586305-17586306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372927838	chr9:17586441-17586442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187805086	chr9:17586469-17586470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7848676	chr9:17586513-17586514	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs531910827	chr9:17586517-17586518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369952393	chr9:17586524-17586525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191109156	chr9:17586533-17586534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142178353	chr9:17586534-17586535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554657259	chr9:17586544-17586545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547129368	chr9:17586578-17586579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143054688	chr9:17586592-17586593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536047710	chr9:17586607-17586608	Weak transcription	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:174 , 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	chr9:17581400-17590000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr9:17584600-17585800	Enhancers	Fetal Brain Female	brain
4	chr9:17585600-17585800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:17585600-17585800	Enhancers	Fetal Brain Male	brain
6	chr9:17585800-17589600	Weak transcription	Fetal Brain Female	brain
7	chr9:17587200-17587400	Enhancers	H1 Cell Line	embryonic stem cell
8	chr9:17588400-17588600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr9:17589600-17589800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
10	chr9:17589600-17590000	Enhancers	Fetal Brain Female	brain
11	chr9:17589800-17590000	Enhancers	Gastric	stomach
12	chr9:17590000-17590600	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr9:17590600-17600400	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr9:17591600-17592000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr9:17591600-17592400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr9:17591600-17592800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr9:17591600-17593000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr9:17591800-17592400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr9:17591800-17592600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr9:17591800-17592600	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr9:17591800-17592800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr9:17592000-17592400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:17592000-17593000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr9:17595200-17595400	Enhancers	Dnd41	blood
25	chr9:17598000-17598200	Enhancers	Psoas Muscle	Psoas
26	chr9:17599200-17599600	Enhancers	Fetal Brain Female	brain
27	chr9:17599400-17599600	Enhancers	Hela-S3	cervix
28	chr9:17599600-17600600	Weak transcription	Hela-S3	cervix
29	chr9:17599800-17600600	Weak transcription	Fetal Heart	heart
30	chr9:17600400-17601200	Enhancers	Fetal Brain Male	brain
31	chr9:17600400-17602200	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr9:17600600-17600800	Enhancers	Fetal Heart	heart
33	chr9:17600600-17602000	Enhancers	Hela-S3	cervix
34	chr9:17600800-17601800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr9:17600800-17607400	Weak transcription	Fetal Heart	heart
36	chr9:17601000-17601600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr9:17601000-17601800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr9:17601000-17601800	Enhancers	NH-A	brain
39	chr9:17602000-17604000	Weak transcription	Hela-S3	cervix
40	chr9:17602200-17608600	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr9:17604000-17605000	Enhancers	Hela-S3	cervix
42	chr9:17605000-17608600	Weak transcription	Hela-S3	cervix
43	chr9:17607400-17613000	Enhancers	Fetal Heart	heart
44	chr9:17608600-17608800	Enhancers	Hela-S3	cervix
45	chr9:17608600-17610800	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr9:17608800-17609200	Weak transcription	Hela-S3	cervix
47	chr9:17609000-17609400	Enhancers	Left Ventricle	heart
48	chr9:17609200-17610000	Enhancers	Hela-S3	cervix
49	chr9:17609800-17610000	Enhancers	Left Ventricle	heart
50	chr9:17609800-17612400	Weak transcription	Fetal Brain Male	brain

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