Variant report

Variant	nsv517380
Chromosome Location	chr9:17564267-17633232
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	ATF2	chr9:17578879-17579258	H1-hESC	embryonic stem cell:	n/a	chr9:17579056-17579070
2	BACH1	chr9:17579465-17579665	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:17578520-17578521	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr9:17615714-17616232	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr9:17630356-17631147	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr9:17627759-17628044	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr9:17614932-17615321	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr9:17579040-17579237	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr9:17578871-17579210	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr9:17592528-17592872	IMR90	lung:	n/a	chr9:17592694-17592705
11	CEBPB	chr9:17629978-17632015	Hela-S3	cervix:	n/a	chr9:17630738-17630751 chr9:17631912-17631925 chr9:17631558-17631566 chr9:17630738-17630749
12	CEBPB	chr9:17614857-17615380	ECC-1	luminal epithelium:	n/a	chr9:17615138-17615149
13	CEBPB	chr9:17587199-17587501	HepG2	liver:	n/a	chr9:17587326-17587337
14	CEBPB	chr9:17614954-17615307	HepG2	liver:	n/a	chr9:17615138-17615149
15	CEBPB	chr9:17623976-17624330	HepG2	liver:	n/a	chr9:17624148-17624159
16	CEBPB	chr9:17587172-17587471	A549	lung:	n/a	chr9:17587326-17587337
17	CEBPB	chr9:17614965-17615325	ECC-1	luminal epithelium:	n/a	chr9:17615138-17615149
18	CEBPB	chr9:17565909-17566256	IMR90	lung:	n/a	chr9:17566093-17566104
19	CEBPB	chr9:17627674-17628045	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:17613398-17614137	Hela-S3	cervix:	n/a	chr9:17613504-17613516
21	CEBPB	chr9:17630600-17630833	H1-hESC	embryonic stem cell:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
22	CEBPB	chr9:17565950-17566237	HepG2	liver:	n/a	chr9:17566093-17566104
23	CEBPB	chr9:17623982-17624335	A549	lung:	n/a	chr9:17624148-17624159
24	CEBPB	chr9:17623986-17624320	IMR90	lung:	n/a	chr9:17624148-17624159
25	CEBPB	chr9:17592528-17592868	HepG2	liver:	n/a	chr9:17592694-17592705
26	CEBPB	chr9:17565992-17566243	H1-hESC	embryonic stem cell:	n/a	chr9:17566093-17566104
27	CEBPB	chr9:17565934-17566222	Hela-S3	cervix:	n/a	chr9:17566093-17566104
28	CEBPB	chr9:17614980-17615315	IMR90	lung:	n/a	chr9:17615138-17615149
29	CEBPB	chr9:17592526-17592860	A549	lung:	n/a	chr9:17592694-17592705
30	CEBPB	chr9:17633008-17633404	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr9:17614983-17615236	MCF-7	breast:	n/a	chr9:17615138-17615149
32	CEBPB	chr9:17594289-17594350	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:17625646-17626018	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr9:17565911-17566238	A549	lung:	n/a	chr9:17566093-17566104
35	CEBPB	chr9:17587171-17587497	H1-hESC	embryonic stem cell:	n/a	chr9:17587326-17587337
36	CEBPB	chr9:17607328-17607618	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr9:17623974-17624320	Hela-S3	cervix:	n/a	chr9:17624148-17624159
38	CEBPB	chr9:17615547-17615651	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr9:17630429-17631023	ECC-1	luminal epithelium:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
40	CEBPB	chr9:17630514-17630924	ECC-1	luminal epithelium:	n/a	chr9:17630738-17630751 chr9:17630738-17630749
41	CEBPB	chr9:17578893-17579163	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr9:17615004-17615229	A549	lung:	n/a	chr9:17615138-17615149
43	CEBPB	chr9:17587142-17587477	ECC-1	luminal epithelium:	n/a	chr9:17587326-17587337
44	CEBPB	chr9:17628638-17629066	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr9:17584689-17584710	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr9:17614997-17615244	H1-hESC	embryonic stem cell:	n/a	chr9:17615138-17615149
47	CEBPB	chr9:17578952-17579084	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr9:17587205-17587469	Hela-S3	cervix:	n/a	chr9:17587326-17587337
49	CEBPB	chr9:17614739-17615763	Hela-S3	cervix:	n/a	chr9:17615138-17615149
50	CHD1	chr9:17579305-17579446	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17578725-17578775	GM12891	blood:	n/a
2	chr9:17578725-17578775	GM12891	blood:	n/a
3	chr9:17591842-17591892	MCF10A-Er-Src	breast:	n/a
4	chr9:17578779-17578829	HCT-116	colon:	n/a
5	chr9:17579026-17579076	PFSK-1	brain:	n/a
6	chr9:17578174-17578224	ovcar-3	ovarian:	n/a
7	chr9:17578174-17578224	GM12892	blood:	n/a
8	chr9:17578174-17578224	MCF-7	breast:	n/a
9	chr9:17578174-17578224	ECC-1	luminal epithelium:	n/a
10	chr9:17579026-17579076	Hela-S3	cervix:	n/a
11	chr9:17591842-17591892	HCF	heart:	n/a
12	chr9:17579026-17579076	GM12891	blood:	n/a
13	chr9:17578725-17578775	PFSK-1	brain:	n/a
14	chr9:17578174-17578224	RPTEC	kidney:	n/a
15	chr9:17579227-17579277	HCF	heart:	n/a
16	chr9:17579734-17579784	AG09319	gingival:	n/a
17	chr9:17578725-17578775	GM06990	blood:	n/a
18	chr9:17591842-17591892	HepG2	liver:	n/a
19	chr9:17579026-17579076	K562	blood:	n/a
20	chr9:17578725-17578775	Hela-S3	cervix:	n/a
21	chr9:17579734-17579784	AG04450	lung:	fetal
22	chr9:17579227-17579277	SAEC	small airway:	n/a
23	chr9:17578779-17578829	HCM	heart:	n/a
24	chr9:17591842-17591892	ECC-1	luminal epithelium:	n/a
25	chr9:17578174-17578224	HEEpiC	esophagus:	n/a
26	chr9:17579227-17579277	T-47D	breast:	n/a
27	chr9:17578779-17578829	CMK	blood:	n/a
28	chr9:17591842-17591892	NT2-D1	testis:	n/a
29	chr9:17578174-17578224	HNPCEpiC	eye:	n/a
30	chr9:17579734-17579784	HAEpiC	amniotic membrane:	n/a
31	chr9:17578174-17578224	HL-60	blood:	n/a
32	chr9:17579026-17579076	ECC-1	luminal epithelium:	n/a
33	chr9:17578779-17578829	H1-hESC	embryonic stem cell:	embryo
34	chr9:17578779-17578829	NHDF-neo	bronchial:	n/a
35	chr9:17578174-17578224	PFSK-1	brain:	n/a
36	chr9:17579227-17579277	BJ	skin:	n/a
37	chr9:17579026-17579076	Caco-2	colon:	n/a
38	chr9:17591842-17591892	NB4	blood:	n/a
39	chr9:17579227-17579277	HRE	kidney:	n/a
40	chr9:17579734-17579784	BE2_C	brain:	n/a
41	chr9:17579734-17579784	HUVEC	blood vessel:	n/a
42	chr9:17578174-17578224	GM12891	blood:	n/a
43	chr9:17579227-17579277	NB4	blood:	n/a
44	chr9:17578779-17578829	GM19239	blood:	n/a
45	chr9:17578725-17578775	BE2_C	brain:	n/a
46	chr9:17591842-17591892	HCPEpiC	choroid plexus:	n/a
47	chr9:17579227-17579277	HIPEpiC	eye:	n/a
48	chr9:17591842-17591892	GM12892	blood:	n/a
49	chr9:17578779-17578829	NB4	blood:	n/a
50	chr9:17578174-17578224	A549	lung:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTLN-5	chr9:17579080-17579285	NONHSAT130304
2	lnc-BNC2-5	chr9:17590903-17591316	NONHSAT130305
3	lnc-BNC2-5	chr9:17589159-17590751	NONHSAT130305
4	lnc-CNTLN-5	chr9:17630352-17630427	NONHSAT130304

Variant related genes	Relation type
SH3GL2	TF binding region
PABPC1P11	TF binding region
SH3GL2	CpG island
PABPC1P11	CpG island

Extended variants
information (count: 3137 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3137 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537934853	chr9:17567616-17567617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs111960433	chr9:17567620-17567621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537480978	chr9:17567696-17567697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145858510	chr9:17567732-17567733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182312960	chr9:17567740-17567741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554418127	chr9:17567750-17567751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549824150	chr9:17567762-17567763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572606085	chr9:17567765-17567766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187071932	chr9:17567820-17567821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571228935	chr9:17567835-17567836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546646720	chr9:17567838-17567839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537001244	chr9:17567841-17567842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149014401	chr9:17567842-17567843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374615938	chr9:17567854-17567855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576023162	chr9:17567894-17567895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10963146	chr9:17567908-17567909	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs191843814	chr9:17567911-17567912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576538746	chr9:17567950-17567951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78451254	chr9:17567954-17567955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559544893	chr9:17567997-17567998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184301053	chr9:17568025-17568026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536547619	chr9:17568058-17568059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561101945	chr9:17568095-17568096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531707123	chr9:17568106-17568107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550217982	chr9:17568112-17568113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571732584	chr9:17568131-17568132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539139930	chr9:17568160-17568161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547672444	chr9:17568170-17568171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189911038	chr9:17568174-17568175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536530139	chr9:17568176-17568177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143830790	chr9:17568222-17568223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141254464	chr9:17568242-17568243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144002361	chr9:17568261-17568262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146466734	chr9:17568291-17568292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193193030	chr9:17568294-17568295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370954273	chr9:17568304-17568305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201173576	chr9:17568307-17568308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185396533	chr9:17568331-17568332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73412649	chr9:17568335-17568336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541677465	chr9:17568337-17568338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563567496	chr9:17568338-17568339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530838030	chr9:17568339-17568340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139189700	chr9:17568350-17568351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565328201	chr9:17568361-17568362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532644717	chr9:17568379-17568380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565295491	chr9:17568397-17568398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540506775	chr9:17568400-17568401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560616382	chr9:17568402-17568403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530286362	chr9:17568429-17568430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548506903	chr9:17568479-17568480	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:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17567600-17571400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:17571200-17571800	Enhancers	H1 Cell Line	embryonic stem cell
3	chr9:17571200-17572200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:17571200-17572600	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr9:17571200-17572600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:17571200-17572600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr9:17571400-17571600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
8	chr9:17571400-17571600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr9:17571400-17571800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr9:17571400-17572000	Enhancers	H9 Cell Line	embryonic stem cell
11	chr9:17571400-17572600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr9:17571600-17571800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
13	chr9:17571600-17572000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr9:17571600-17572000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:17571600-17572200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
16	chr9:17571600-17572400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr9:17571600-17572400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr9:17571800-17572000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
19	chr9:17571800-17572000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr9:17572000-17572400	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr9:17573600-17574000	Enhancers	HSMMtube	muscle
22	chr9:17574400-17575000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr9:17577800-17578000	Enhancers	Esophagus	oesophagus
24	chr9:17577800-17578200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr9:17577800-17578200	Active TSS	Spleen	Spleen
26	chr9:17577800-17580000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
27	chr9:17578000-17578200	Bivalent/Poised TSS	Fetal Intestine Small	intestine
28	chr9:17578200-17578400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr9:17578200-17578400	Enhancers	Hela-S3	cervix
30	chr9:17578200-17578600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
31	chr9:17578200-17578600	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
32	chr9:17578200-17578600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
33	chr9:17578200-17578600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr9:17578200-17578800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
35	chr9:17578200-17579000	Bivalent/Poised TSS	Ovary	ovary
36	chr9:17578200-17580000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr9:17578200-17580600	Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr9:17578400-17578600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
39	chr9:17578400-17578600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr9:17578400-17578600	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
41	chr9:17578400-17578600	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr9:17578400-17578600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr9:17578400-17578600	Bivalent Enhancer	Adipose Nuclei	Adipose
44	chr9:17578400-17578600	Enhancers	Brain Hippocampus Middle	brain
45	chr9:17578400-17578600	Active TSS	Brain Inferior Temporal Lobe	brain
46	chr9:17578400-17578600	Enhancers	Brain Substantia Nigra	brain
47	chr9:17578400-17578600	Bivalent Enhancer	Fetal Kidney	kidney
48	chr9:17578400-17578600	Bivalent Enhancer	Fetal Lung	lung
49	chr9:17578400-17578600	Enhancers	Right Ventricle	heart
50	chr9:17578400-17578600	Bivalent Enhancer	HUVEC	blood vessel

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