Variant report

Variant	esv2764160
Chromosome Location	chr9:17581422-17636674
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	chr9:17614932-17615321	Hela-S3	cervix:	n/a	n/a
2	BRCA1	chr9:17630356-17631147	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr9:17627759-17628044	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr9:17615714-17616232	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr9:17587205-17587469	Hela-S3	cervix:	n/a	chr9:17587326-17587337
6	CEBPB	chr9:17587171-17587497	H1-hESC	embryonic stem cell:	n/a	chr9:17587326-17587337
7	CEBPB	chr9:17630429-17631023	ECC-1	luminal epithelium:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
8	CEBPB	chr9:17614980-17615315	IMR90	lung:	n/a	chr9:17615138-17615149
9	CEBPB	chr9:17613398-17614137	Hela-S3	cervix:	n/a	chr9:17613504-17613516
10	CEBPB	chr9:17592528-17592872	IMR90	lung:	n/a	chr9:17592694-17592705
11	CEBPB	chr9:17614857-17615380	ECC-1	luminal epithelium:	n/a	chr9:17615138-17615149
12	CEBPB	chr9:17629978-17632015	Hela-S3	cervix:	n/a	chr9:17630738-17630751 chr9:17631912-17631925 chr9:17631558-17631566 chr9:17630738-17630749
13	CEBPB	chr9:17614739-17615763	Hela-S3	cervix:	n/a	chr9:17615138-17615149
14	CEBPB	chr9:17636332-17636742	Hela-S3	cervix:	n/a	chr9:17636377-17636389
15	CEBPB	chr9:17627674-17628045	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr9:17634897-17635195	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr9:17633008-17633404	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr9:17615004-17615229	A549	lung:	n/a	chr9:17615138-17615149
19	CEBPB	chr9:17607328-17607618	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:17630514-17630924	ECC-1	luminal epithelium:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
21	CEBPB	chr9:17630600-17630833	H1-hESC	embryonic stem cell:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
22	CEBPB	chr9:17592526-17592860	A549	lung:	n/a	chr9:17592694-17592705
23	CEBPB	chr9:17614983-17615236	MCF-7	breast:	n/a	chr9:17615138-17615149
24	CEBPB	chr9:17614965-17615325	ECC-1	luminal epithelium:	n/a	chr9:17615138-17615149
25	CEBPB	chr9:17623986-17624320	IMR90	lung:	n/a	chr9:17624148-17624159
26	CEBPB	chr9:17623974-17624320	Hela-S3	cervix:	n/a	chr9:17624148-17624159
27	CEBPB	chr9:17614954-17615307	HepG2	liver:	n/a	chr9:17615138-17615149
28	CEBPB	chr9:17587142-17587477	ECC-1	luminal epithelium:	n/a	chr9:17587326-17587337
29	CEBPB	chr9:17614997-17615244	H1-hESC	embryonic stem cell:	n/a	chr9:17615138-17615149
30	CEBPB	chr9:17587172-17587471	A549	lung:	n/a	chr9:17587326-17587337
31	CEBPB	chr9:17625646-17626018	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr9:17592528-17592868	HepG2	liver:	n/a	chr9:17592694-17592705
33	CEBPB	chr9:17584689-17584710	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr9:17615547-17615651	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr9:17594289-17594350	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:17623982-17624335	A549	lung:	n/a	chr9:17624148-17624159
37	CEBPB	chr9:17623976-17624330	HepG2	liver:	n/a	chr9:17624148-17624159
38	CEBPB	chr9:17628638-17629066	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr9:17587199-17587501	HepG2	liver:	n/a	chr9:17587326-17587337
40	CEBPB	chr9:17634991-17635180	A549	lung:	n/a	n/a
41	CHD2	chr9:17625614-17625983	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr9:17627701-17628040	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr9:17614881-17615285	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr9:17630387-17631090	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr9:17609660-17609810	BJ	skin:	n/a	n/a
46	CTCF	chr9:17622440-17622590	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr9:17588440-17588590	HMEC	breast:	n/a	n/a
48	CTCF	chr9:17622440-17622590	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr9:17622400-17622550	GM06990	blood:	n/a	n/a
50	CTCF	chr9:17587260-17587410	WERI-Rb-1	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17591842-17591892	HL-60	blood:	n/a
2	chr9:17591842-17591892	NT2-D1	testis:	n/a
3	chr9:17591842-17591892	AG10803	skin:	n/a
4	chr9:17591842-17591892	HCM	heart:	n/a
5	chr9:17591842-17591892	AG04450	lung:	fetal
6	chr9:17591842-17591892	SKMC	muscle:	n/a
7	chr9:17591842-17591892	BE2_C	brain:	n/a
8	chr9:17591842-17591892	T-47D	breast:	n/a
9	chr9:17591842-17591892	A549	lung:	n/a
10	chr9:17591842-17591892	Hepatocyte	liver:	n/a
11	chr9:17591842-17591892	U87	brain:	n/a
12	chr9:17591842-17591892	GM12878	blood:	n/a
13	chr9:17591842-17591892	IMR90	lung:	fetal
14	chr9:17591842-17591892	HCPEpiC	choroid plexus:	n/a
15	chr9:17591842-17591892	PrEC	prostate:	n/a
16	chr9:17591842-17591892	NHBE	bronchial:	n/a
17	chr9:17591842-17591892	AG04449	skin:	fetal
18	chr9:17591842-17591892	HUVEC	blood vessel:	n/a
19	chr9:17591842-17591892	CMK	blood:	n/a
20	chr9:17591842-17591892	ovcar-3	ovarian:	n/a
21	chr9:17591842-17591892	GM19239	blood:	n/a
22	chr9:17591842-17591892	GM12891	blood:	n/a
23	chr9:17591842-17591892	NB4	blood:	n/a
24	chr9:17591842-17591892	K562	blood:	n/a
25	chr9:17591842-17591892	Hela-S3	cervix:	n/a
26	chr9:17591842-17591892	GM06990	blood:	n/a
27	chr9:17591842-17591892	Caco-2	colon:	n/a
28	chr9:17591842-17591892	HRE	kidney:	n/a
29	chr9:17591842-17591892	NH-A	brain:	n/a
30	chr9:17591842-17591892	HCT-116	colon:	n/a
31	chr9:17591842-17591892	HRCEpiC	kidney:	n/a
32	chr9:17591842-17591892	AG09319	gingival:	n/a
33	chr9:17591842-17591892	MCF-7	breast:	n/a
34	chr9:17591842-17591892	AG09309	skin:	n/a
35	chr9:17591842-17591892	HNPCEpiC	eye:	n/a
36	chr9:17591842-17591892	SK-N-SH	brain:	n/a
37	chr9:17591842-17591892	RPTEC	kidney:	n/a
38	chr9:17591842-17591892	ProgFib	skin:	n/a
39	chr9:17591842-17591892	Jurkat	blood:	n/a
40	chr9:17591842-17591892	ECC-1	luminal epithelium:	n/a
41	chr9:17591842-17591892	HEK293	kidney:	embryo
42	chr9:17591842-17591892	LNCaP	prostate:	n/a
43	chr9:17591842-17591892	SK-N-MC	brain:	n/a
44	chr9:17591842-17591892	BJ	skin:	n/a
45	chr9:17591842-17591892	GM12892	blood:	n/a
46	chr9:17591842-17591892	HAEpiC	amniotic membrane:	n/a
47	chr9:17591842-17591892	AoSMC	blood vessel:	n/a
48	chr9:17591842-17591892	MCF10A-Er-Src	breast:	n/a
49	chr9:17591842-17591892	HPAEpiC	pulmonary alveolar:	n/a
50	chr9:17591842-17591892	HCF	heart:	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: 2757 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2757 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192006117	chr9:17581424-17581425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs146944328	chr9:17581487-17581488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565235247	chr9:17581488-17581489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138056865	chr9:17581493-17581494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565368070	chr9:17581494-17581495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529716843	chr9:17581498-17581499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547946328	chr9:17581507-17581508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569744989	chr9:17581521-17581522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566926260	chr9:17581579-17581580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113838088	chr9:17581580-17581581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574724334	chr9:17581598-17581599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183517004	chr9:17581617-17581618	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs7030014	chr9:17581661-17581662	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs376203588	chr9:17581705-17581706	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs143404706	chr9:17581706-17581707	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs143891081	chr9:17581757-17581758	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs78496703	chr9:17581763-17581764	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs148618134	chr9:17581779-17581780	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs186688976	chr9:17581781-17581782	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs572434458	chr9:17581798-17581799	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs543016351	chr9:17581809-17581810	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs141982348	chr9:17581833-17581834	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs150695379	chr9:17581834-17581835	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs191602846	chr9:17581837-17581838	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs566136682	chr9:17581857-17581858	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs533631295	chr9:17581869-17581870	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs543645200	chr9:17581905-17581906	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs565174502	chr9:17581914-17581915	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs139834287	chr9:17581916-17581917	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs541300558	chr9:17581944-17581945	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs555075668	chr9:17581949-17581950	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs529620486	chr9:17581988-17581989	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs548173768	chr9:17581992-17581993	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs368895858	chr9:17582155-17582156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569638428	chr9:17582157-17582158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73418611	chr9:17582166-17582167	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs146812561	chr9:17582184-17582185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139643033	chr9:17582234-17582235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs3840725	chr9:17582278-17582279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs10541248	chr9:17582280-17582281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs397765287	chr9:17582284-17582285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182639844	chr9:17582305-17582306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140303267	chr9:17582314-17582315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187204249	chr9:17582321-17582322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs72713327	chr9:17582341-17582342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556339423	chr9:17582355-17582356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553263242	chr9:17582390-17582391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs193016989	chr9:17582401-17582402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369751648	chr9:17582403-17582404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185258632	chr9:17582431-17582432	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:187 , 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	chr9:17581000-17581600	Enhancers	Fetal Brain Female	brain
3	chr9:17581000-17581600	Enhancers	Hela-S3	cervix
4	chr9:17581000-17583600	Weak transcription	Brain Angular Gyrus	brain
5	chr9:17581400-17590000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr9:17581600-17582000	Active TSS	Fetal Brain Female	brain
7	chr9:17581600-17583200	Weak transcription	Hela-S3	cervix
8	chr9:17582000-17582400	Enhancers	Fetal Brain Male	brain
9	chr9:17582000-17584600	Weak transcription	Fetal Brain Female	brain
10	chr9:17582400-17582600	Weak transcription	Fetal Brain Male	brain
11	chr9:17582600-17583000	Enhancers	Fetal Brain Male	brain
12	chr9:17583000-17584000	Weak transcription	Fetal Brain Male	brain
13	chr9:17583200-17583800	Enhancers	Hela-S3	cervix
14	chr9:17584600-17585800	Enhancers	Fetal Brain Female	brain
15	chr9:17585600-17585800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:17585600-17585800	Enhancers	Fetal Brain Male	brain
17	chr9:17585800-17589600	Weak transcription	Fetal Brain Female	brain
18	chr9:17587200-17587400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr9:17588400-17588600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr9:17589600-17589800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
21	chr9:17589600-17590000	Enhancers	Fetal Brain Female	brain
22	chr9:17589800-17590000	Enhancers	Gastric	stomach
23	chr9:17590000-17590600	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr9:17590600-17600400	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr9:17591600-17592000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr9:17591600-17592400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr9:17591600-17592800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr9:17591600-17593000	Enhancers	H1 Cell Line	embryonic stem cell
29	chr9:17591800-17592400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr9:17591800-17592600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr9:17591800-17592600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr9:17591800-17592800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr9:17592000-17592400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr9:17592000-17593000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr9:17595200-17595400	Enhancers	Dnd41	blood
36	chr9:17598000-17598200	Enhancers	Psoas Muscle	Psoas
37	chr9:17599200-17599600	Enhancers	Fetal Brain Female	brain
38	chr9:17599400-17599600	Enhancers	Hela-S3	cervix
39	chr9:17599600-17600600	Weak transcription	Hela-S3	cervix
40	chr9:17599800-17600600	Weak transcription	Fetal Heart	heart
41	chr9:17600400-17601200	Enhancers	Fetal Brain Male	brain
42	chr9:17600400-17602200	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr9:17600600-17600800	Enhancers	Fetal Heart	heart
44	chr9:17600600-17602000	Enhancers	Hela-S3	cervix
45	chr9:17600800-17601800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr9:17600800-17607400	Weak transcription	Fetal Heart	heart
47	chr9:17601000-17601600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr9:17601000-17601800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr9:17601000-17601800	Enhancers	NH-A	brain
50	chr9:17602000-17604000	Weak transcription	Hela-S3	cervix

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