Variant report

Variant	nsv892673
Chromosome Location	chr9:17591830-17624902
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:171)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:171 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr9:17614932-17615321	Hela-S3	cervix:	n/a	n/a
2	BRCA1	chr9:17615714-17616232	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr9:17623986-17624320	IMR90	lung:	n/a	chr9:17624148-17624159
4	CEBPB	chr9:17592526-17592860	A549	lung:	n/a	chr9:17592694-17592705
5	CEBPB	chr9:17614983-17615236	MCF-7	breast:	n/a	chr9:17615138-17615149
6	CEBPB	chr9:17607328-17607618	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr9:17614997-17615244	H1-hESC	embryonic stem cell:	n/a	chr9:17615138-17615149
8	CEBPB	chr9:17614980-17615315	IMR90	lung:	n/a	chr9:17615138-17615149
9	CEBPB	chr9:17615004-17615229	A549	lung:	n/a	chr9:17615138-17615149
10	CEBPB	chr9:17623982-17624335	A549	lung:	n/a	chr9:17624148-17624159
11	CEBPB	chr9:17614954-17615307	HepG2	liver:	n/a	chr9:17615138-17615149
12	CEBPB	chr9:17614739-17615763	Hela-S3	cervix:	n/a	chr9:17615138-17615149
13	CEBPB	chr9:17592528-17592868	HepG2	liver:	n/a	chr9:17592694-17592705
14	CEBPB	chr9:17623974-17624320	Hela-S3	cervix:	n/a	chr9:17624148-17624159
15	CEBPB	chr9:17614965-17615325	ECC-1	luminal epithelium:	n/a	chr9:17615138-17615149
16	CEBPB	chr9:17592528-17592872	IMR90	lung:	n/a	chr9:17592694-17592705
17	CEBPB	chr9:17613398-17614137	Hela-S3	cervix:	n/a	chr9:17613504-17613516
18	CEBPB	chr9:17623976-17624330	HepG2	liver:	n/a	chr9:17624148-17624159
19	CEBPB	chr9:17615547-17615651	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr9:17594289-17594350	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:17614857-17615380	ECC-1	luminal epithelium:	n/a	chr9:17615138-17615149
22	CHD2	chr9:17614881-17615285	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr9:17622460-17622610	HAc	cerebellar:	n/a	n/a
24	CTCF	chr9:17622456-17622579	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr9:17593261-17593310	ProgFib	skin:	n/a	n/a
26	CTCF	chr9:17622440-17622590	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr9:17622480-17622630	HRE	kidney:	n/a	n/a
28	CTCF	chr9:17617720-17617870	NHLF	lung:	n/a	n/a
29	CTCF	chr9:17609660-17609810	BJ	skin:	n/a	n/a
30	CTCF	chr9:17622440-17622590	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr9:17598560-17598710	NB4	blood:	n/a	n/a
32	CTCF	chr9:17622500-17622650	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr9:17622220-17622370	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr9:17615089-17615258	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr9:17609731-17609830	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr9:17622400-17622550	RPTEC	kidney:	n/a	n/a
37	CTCF	chr9:17604029-17604034	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr9:17609720-17609870	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr9:17622400-17622550	GM06990	blood:	n/a	n/a
40	CTCF	chr9:17622380-17622530	HEK293	kidney:	n/a	n/a
41	E2F4	chr9:17621649-17621805	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr9:17613734-17614001	MCF10A-Er-Src	breast:	n/a	n/a
43	ELK1	chr9:17614991-17615279	Hela-S3	cervix:	n/a	n/a
44	ELK4	chr9:17601188-17601443	Hela-S3	cervix:	n/a	n/a
45	EP300	chr9:17616117-17616462	Hela-S3	cervix:	n/a	n/a
46	EP300	chr9:17614828-17615332	Hela-S3	cervix:	n/a	n/a
47	EP300	chr9:17613463-17614202	Hela-S3	cervix:	n/a	n/a
48	FOS	chr9:17613680-17614100	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr9:17613680-17614061	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr9:17601173-17601612	MCF10A-Er-Src	breast:	n/a	chr9:17601391-17601399 chr9:17601527-17601536 chr9:17601389-17601400 chr9:17601391-17601398 chr9:17601392-17601403

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17591842-17591892	AG09309	skin:	n/a
2	chr9:17591842-17591892	SKMC	muscle:	n/a
3	chr9:17591842-17591892	HIPEpiC	eye:	n/a
4	chr9:17591842-17591892	GM06990	blood:	n/a
5	chr9:17591842-17591892	HCPEpiC	choroid plexus:	n/a
6	chr9:17591842-17591892	HEEpiC	esophagus:	n/a
7	chr9:17591842-17591892	HNPCEpiC	eye:	n/a
8	chr9:17591842-17591892	NH-A	brain:	n/a
9	chr9:17591842-17591892	T-47D	breast:	n/a
10	chr9:17591842-17591892	BE2_C	brain:	n/a
11	chr9:17591842-17591892	NHDF-neo	bronchial:	n/a
12	chr9:17591842-17591892	HCF	heart:	n/a
13	chr9:17591842-17591892	ProgFib	skin:	n/a
14	chr9:17591842-17591892	MCF-7	breast:	n/a
15	chr9:17591842-17591892	AG09319	gingival:	n/a
16	chr9:17591842-17591892	HL-60	blood:	n/a
17	chr9:17591842-17591892	IMR90	lung:	fetal
18	chr9:17591842-17591892	Jurkat	blood:	n/a
19	chr9:17591842-17591892	Hepatocyte	liver:	n/a
20	chr9:17591842-17591892	HEK293	kidney:	embryo
21	chr9:17591842-17591892	Caco-2	colon:	n/a
22	chr9:17591842-17591892	PFSK-1	brain:	n/a
23	chr9:17591842-17591892	GM12878	blood:	n/a
24	chr9:17591842-17591892	PrEC	prostate:	n/a
25	chr9:17591842-17591892	AG04450	lung:	fetal
26	chr9:17591842-17591892	HUVEC	blood vessel:	n/a
27	chr9:17591842-17591892	Hela-S3	cervix:	n/a
28	chr9:17591842-17591892	MCF10A-Er-Src	breast:	n/a
29	chr9:17591842-17591892	NT2-D1	testis:	n/a
30	chr9:17591842-17591892	HRPEpiC	eye:	n/a
31	chr9:17591842-17591892	HRCEpiC	kidney:	n/a
32	chr9:17591842-17591892	SAEC	small airway:	n/a
33	chr9:17591842-17591892	A549	lung:	n/a
34	chr9:17591842-17591892	AoSMC	blood vessel:	n/a
35	chr9:17591842-17591892	ECC-1	luminal epithelium:	n/a
36	chr9:17591842-17591892	K562	blood:	n/a
37	chr9:17591842-17591892	HMEC	breast:	n/a
38	chr9:17591842-17591892	BJ	skin:	n/a
39	chr9:17591842-17591892	SK-N-SH_RA	brain:	n/a
40	chr9:17591842-17591892	GM19239	blood:	n/a
41	chr9:17591842-17591892	SK-N-SH	brain:	n/a
42	chr9:17591842-17591892	CMK	blood:	n/a
43	chr9:17591842-17591892	AG10803	skin:	n/a
44	chr9:17591842-17591892	LNCaP	prostate:	n/a
45	chr9:17591842-17591892	GM12891	blood:	n/a
46	chr9:17591842-17591892	HAEpiC	amniotic membrane:	n/a
47	chr9:17591842-17591892	U87	brain:	n/a
48	chr9:17591842-17591892	H1-hESC	embryonic stem cell:	embryo
49	chr9:17591842-17591892	HPAEpiC	pulmonary alveolar:	n/a
50	chr9:17591842-17591892	NHBE	bronchial:	n/a

No data

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

Extended variants
information (count: 1689 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1689 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4961575	chr9:17591830-17591831	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572577038	chr9:17591837-17591838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78148565	chr9:17591842-17591843	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs138432199	chr9:17591854-17591855	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs143820276	chr9:17591888-17591889	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs376568598	chr9:17591921-17591922	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs184595779	chr9:17591923-17591924	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs189209505	chr9:17591932-17591933	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs564807442	chr9:17591946-17591947	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs116957541	chr9:17591978-17591979	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs147252607	chr9:17591984-17591985	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs139702656	chr9:17591990-17591991	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs542228103	chr9:17592001-17592002	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs10963154	chr9:17592008-17592009	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs181861437	chr9:17592018-17592019	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs548461092	chr9:17592036-17592037	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs553084198	chr9:17592050-17592051	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs370622368	chr9:17592072-17592073	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs538238279	chr9:17592082-17592083	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs187670335	chr9:17592112-17592113	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs577973384	chr9:17592137-17592138	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs539095918	chr9:17592146-17592147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553980609	chr9:17592156-17592157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374370875	chr9:17592183-17592184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74505109	chr9:17592187-17592188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561243837	chr9:17592211-17592212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116400424	chr9:17592250-17592251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149314775	chr9:17592260-17592261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372953312	chr9:17592261-17592262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549374312	chr9:17592296-17592297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189141330	chr9:17592400-17592401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs180952608	chr9:17592407-17592408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557288514	chr9:17592456-17592457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186174830	chr9:17592464-17592465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559191952	chr9:17592563-17592564	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs529902593	chr9:17592578-17592579	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs575853704	chr9:17592632-17592633	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs548448630	chr9:17592709-17592710	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs376068756	chr9:17592714-17592715	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs537309480	chr9:17592727-17592728	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs200019101	chr9:17592733-17592734	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs552212051	chr9:17592738-17592739	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs571573789	chr9:17592793-17592794	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs190202428	chr9:17592816-17592817	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs182641960	chr9:17592817-17592818	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs185769716	chr9:17592878-17592879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536427788	chr9:17592888-17592889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554777067	chr9:17592901-17592902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530709536	chr9:17592905-17592906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576243933	chr9:17592914-17592915	Enhancers 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:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17590600-17600400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr9:17591600-17592000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr9:17591600-17592400	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr9:17591600-17592800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr9:17591600-17593000	Enhancers	H1 Cell Line	embryonic stem cell
6	chr9:17591800-17592400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr9:17591800-17592600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr9:17591800-17592600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr9:17591800-17592800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr9:17592000-17592400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr9:17592000-17593000	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr9:17595200-17595400	Enhancers	Dnd41	blood
13	chr9:17598000-17598200	Enhancers	Psoas Muscle	Psoas
14	chr9:17599200-17599600	Enhancers	Fetal Brain Female	brain
15	chr9:17599400-17599600	Enhancers	Hela-S3	cervix
16	chr9:17599600-17600600	Weak transcription	Hela-S3	cervix
17	chr9:17599800-17600600	Weak transcription	Fetal Heart	heart
18	chr9:17600400-17601200	Enhancers	Fetal Brain Male	brain
19	chr9:17600400-17602200	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr9:17600600-17600800	Enhancers	Fetal Heart	heart
21	chr9:17600600-17602000	Enhancers	Hela-S3	cervix
22	chr9:17600800-17601800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr9:17600800-17607400	Weak transcription	Fetal Heart	heart
24	chr9:17601000-17601600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr9:17601000-17601800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr9:17601000-17601800	Enhancers	NH-A	brain
27	chr9:17602000-17604000	Weak transcription	Hela-S3	cervix
28	chr9:17602200-17608600	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr9:17604000-17605000	Enhancers	Hela-S3	cervix
30	chr9:17605000-17608600	Weak transcription	Hela-S3	cervix
31	chr9:17607400-17613000	Enhancers	Fetal Heart	heart
32	chr9:17608600-17608800	Enhancers	Hela-S3	cervix
33	chr9:17608600-17610800	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr9:17608800-17609200	Weak transcription	Hela-S3	cervix
35	chr9:17609000-17609400	Enhancers	Left Ventricle	heart
36	chr9:17609200-17610000	Enhancers	Hela-S3	cervix
37	chr9:17609800-17610000	Enhancers	Left Ventricle	heart
38	chr9:17609800-17612400	Weak transcription	Fetal Brain Male	brain
39	chr9:17610000-17611400	Weak transcription	Hela-S3	cervix
40	chr9:17610800-17611800	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr9:17611400-17612000	Enhancers	Hela-S3	cervix
42	chr9:17611600-17612200	Enhancers	Left Ventricle	heart
43	chr9:17611800-17613600	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr9:17611800-17615200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr9:17612000-17612200	Enhancers	Brain Germinal Matrix	brain
46	chr9:17612000-17612400	Flanking Active TSS	Hela-S3	cervix
47	chr9:17612000-17615200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr9:17612200-17613600	Weak transcription	Brain Germinal Matrix	brain
49	chr9:17612400-17612600	Enhancers	Brain Anterior Caudate	brain
50	chr9:17612400-17613400	Enhancers	Hela-S3	cervix

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