Variant report

Variant	nsv613708
Chromosome Location	chr9:17720175-18072085
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	ARID3A	chr9:18059523-18059713	HepG2	liver:	n/a	n/a
2	ATF1	chr9:17794285-17794535	K562	blood:	n/a	n/a
3	ATF1	chr9:17799480-17799680	K562	blood:	n/a	n/a
4	ATF1	chr9:17795665-17796153	K562	blood:	n/a	n/a
5	ATF2	chr9:17863016-17863724	GM12878	blood:	n/a	n/a
6	ATF2	chr9:17741979-17742453	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:17863044-17863731	GM12878	blood:	n/a	n/a
8	ATF2	chr9:18056984-18057335	GM12878	blood:	n/a	n/a
9	BACH1	chr9:17906975-17907143	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:17906012-17906129	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr9:17876691-17876948	GM12878	blood:	n/a	n/a
12	BATF	chr9:17863100-17863547	GM12878	blood:	n/a	n/a
13	BATF	chr9:18057009-18057305	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:17863045-17863660	GM12878	blood:	n/a	chr9:17863293-17863302
15	BCL11A	chr9:17863162-17863611	GM12878	blood:	n/a	chr9:17863293-17863302
16	BCL3	chr9:17816222-17816399	GM12878	blood:	n/a	n/a
17	BHLHE40	chr9:18057045-18057366	GM12878	blood:	n/a	n/a
18	BHLHE40	chr9:17811041-17811342	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:17863153-17863948	GM12878	blood:	n/a	n/a
20	BRCA1	chr9:18038580-18038795	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr9:17996799-17997233	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr9:17900404-17901108	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr9:17810992-17811324	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr9:17962682-17963058	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr9:18055933-18056074	Hela-S3	cervix:	n/a	chr9:18055960-18055971 chr9:18055960-18055973
26	CEBPB	chr9:17848447-17848741	HepG2	liver:	n/a	n/a
27	CEBPB	chr9:17805161-17805386	HepG2	liver:	n/a	chr9:17805311-17805322
28	CEBPB	chr9:18038793-18038875	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr9:17927715-17927933	HepG2	liver:	n/a	chr9:17927753-17927764
30	CEBPB	chr9:18059118-18059439	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr9:17772274-17772617	ECC-1	luminal epithelium:	n/a	chr9:17772409-17772420
32	CEBPB	chr9:17772235-17772603	HepG2	liver:	n/a	chr9:17772409-17772420
33	CEBPB	chr9:17772244-17772602	IMR90	lung:	n/a	chr9:17772409-17772420
34	CEBPB	chr9:17994719-17995006	HepG2	liver:	n/a	chr9:17994871-17994882 chr9:17994871-17994884 chr9:17994873-17994882 chr9:17994873-17994884
35	CEBPB	chr9:17782739-17783093	K562	blood:	n/a	chr9:17782917-17782928
36	CEBPB	chr9:17958086-17958417	HepG2	liver:	n/a	chr9:17958254-17958265 chr9:17958254-17958267
37	CEBPB	chr9:17906776-17906923	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr9:17782732-17783112	A549	lung:	n/a	chr9:17782917-17782928
39	CEBPB	chr9:17845954-17846094	Hela-S3	cervix:	n/a	chr9:17846001-17846012 chr9:17845999-17846010
40	CEBPB	chr9:17922306-17922493	IMR90	lung:	n/a	chr9:17922368-17922381 chr9:17922370-17922381 chr9:17922368-17922379 chr9:17922368-17922381
41	CEBPB	chr9:17782739-17783101	H1-hESC	embryonic stem cell:	n/a	chr9:17782917-17782928
42	CEBPB	chr9:18048356-18048587	HepG2	liver:	n/a	chr9:18048517-18048528
43	CEBPB	chr9:17894021-17894317	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr9:18055815-18056121	HepG2	liver:	n/a	chr9:18055960-18055971 chr9:18055960-18055973
45	CEBPB	chr9:17772240-17772598	K562	blood:	n/a	chr9:17772409-17772420
46	CEBPB	chr9:18059218-18059418	HepG2	liver:	n/a	n/a
47	CEBPB	chr9:17805157-17805464	IMR90	lung:	n/a	chr9:17805311-17805322
48	CEBPB	chr9:17782751-17783101	Hela-S3	cervix:	n/a	chr9:17782917-17782928
49	CEBPB	chr9:17955369-17956267	Hela-S3	cervix:	n/a	chr9:17955902-17955913 chr9:17956114-17956125 chr9:17956114-17956127 chr9:17956114-17956127 chr9:17956217-17956229
50	CEBPB	chr9:18068726-18068788	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17906561-17906611	GM12892	blood:	n/a
2	chr9:17906561-17906611	PANC-1	pancreas:	n/a
3	chr9:17906561-17906611	AG09309	skin:	n/a
4	chr9:17907485-17907535	ProgFib	skin:	n/a
5	chr9:17906113-17906163	Hela-S3	cervix:	n/a
6	chr9:17906561-17906611	HNPCEpiC	eye:	n/a
7	chr9:17906561-17906611	GM06990	blood:	n/a
8	chr9:17906113-17906163	PrEC	prostate:	n/a
9	chr9:17907018-17907068	IMR90	lung:	fetal
10	chr9:17907163-17907213	HIPEpiC	eye:	n/a
11	chr9:17907018-17907068	Hela-S3	cervix:	n/a
12	chr9:17907163-17907213	HPAEpiC	pulmonary alveolar:	n/a
13	chr9:17906338-17906388	HCM	heart:	n/a
14	chr9:17906338-17906388	CMK	blood:	n/a
15	chr9:17906561-17906611	HAEpiC	amniotic membrane:	n/a
16	chr9:17906561-17906611	AG10803	skin:	n/a
17	chr9:17796830-17796880	GM12891	blood:	n/a
18	chr9:17906561-17906611	HCF	heart:	n/a
19	chr9:17907163-17907213	GM12878	blood:	n/a
20	chr9:17906561-17906611	HL-60	blood:	n/a
21	chr9:17907485-17907535	PFSK-1	brain:	n/a
22	chr9:17907485-17907535	HCPEpiC	choroid plexus:	n/a
23	chr9:17907018-17907068	NB4	blood:	n/a
24	chr9:17907018-17907068	HAEpiC	amniotic membrane:	n/a
25	chr9:17796830-17796880	CMK	blood:	n/a
26	chr9:17907018-17907068	NHDF-neo	bronchial:	n/a
27	chr9:17907485-17907535	Caco-2	colon:	n/a
28	chr9:17906338-17906388	HRE	kidney:	n/a
29	chr9:17906113-17906163	ProgFib	skin:	n/a
30	chr9:17907163-17907213	Hela-S3	cervix:	n/a
31	chr9:17906338-17906388	HUVEC	blood vessel:	n/a
32	chr9:17906113-17906163	HEK293	kidney:	embryo
33	chr9:17906338-17906388	GM12891	blood:	n/a
34	chr9:17906113-17906163	MCF10A-Er-Src	breast:	n/a
35	chr9:17907163-17907213	AG09309	skin:	n/a
36	chr9:17906561-17906611	Hela-S3	cervix:	n/a
37	chr9:17796830-17796880	HEK293	kidney:	embryo
38	chr9:17907163-17907213	AG09319	gingival:	n/a
39	chr9:17906561-17906611	SKMC	muscle:	n/a
40	chr9:17907485-17907535	HAEpiC	amniotic membrane:	n/a
41	chr9:17906561-17906611	MCF-7	breast:	n/a
42	chr9:17907163-17907213	Jurkat	blood:	n/a
43	chr9:17907485-17907535	SK-N-SH_RA	brain:	n/a
44	chr9:17906338-17906388	BJ	skin:	n/a
45	chr9:17907163-17907213	A549	lung:	n/a
46	chr9:17906561-17906611	HPAEpiC	pulmonary alveolar:	n/a
47	chr9:17907163-17907213	SK-N-SH	brain:	n/a
48	chr9:17907018-17907068	HCT-116	colon:	n/a
49	chr9:17906338-17906388	U87	brain:	n/a
50	chr9:17906113-17906163	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:17531556..17532244-chr9:17793906..17794864,2	MCF-7	breast:
2	chr1:200018379..200019256-chr9:18037438..18038367,2	MCF-7	breast:
3	chr9:17531221..17532407-chr9:17801949..17802935,11	MCF-7	breast:
4	chr9:17811052..17811931-chr9:18212974..18213863,4	MCF-7	breast:
5	chr9:17810623..17811776-chr9:18207859..18208526,4	MCF-7	breast:
6	chr9:17822817..17825077-chr9:17826697..17828392,2	K562	blood:
7	chr9:18016854..18017748-chr9:18207853..18208432,2	MCF-7	breast:
8	chr9:17528626..17529303-chr9:17802052..17802868,3	MCF-7	breast:
9	chr10:33352554..33353197-chr9:17810608..17811353,2	MCF-7	breast:
10	chr9:17822817..17825077-chr9:17826697..17828392,2	K562	blood:
11	chr9:17810712..17811652-chr9:18207926..18208828,3	MCF-7	breast:
12	chr6:74564419..74565369-chr9:17774545..17775065,2	K562	blood:
13	chr9:17531792..17532337-chr9:17794326..17794832,2	MCF-7	breast:
14	chr9:17531372..17532326-chr9:17801979..17802845,5	MCF-7	breast:

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

Extended variants
information (count: 13756 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:13756 , 50 per page) page: 1 2 3 4 5 6 7 ... 276

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553619962	chr9:17720801-17720802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566545025	chr9:17720813-17720814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373665926	chr9:17720824-17720825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534158015	chr9:17720855-17720856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10114474	chr9:17720884-17720885	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs574127064	chr9:17720889-17720890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537944817	chr9:17720957-17720958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370497063	chr9:17721005-17721006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147498069	chr9:17721062-17721063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73645153	chr9:17721064-17721065	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs78459270	chr9:17721066-17721067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560725418	chr9:17721099-17721100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73645154	chr9:17721176-17721177	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs542654354	chr9:17721180-17721181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560709562	chr9:17721194-17721195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187886900	chr9:17721860-17721861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148749087	chr9:17721872-17721873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566117017	chr9:17721878-17721879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192976363	chr9:17721881-17721882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554928919	chr9:17721890-17721891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575998825	chr9:17721948-17721949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542968785	chr9:17721950-17721951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558129801	chr9:17721954-17721955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs57799581	chr9:17722066-17722067	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs11790692	chr9:17722069-17722070	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs183379126	chr9:17722075-17722076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs143548602	chr9:17722104-17722105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542125235	chr9:17722120-17722121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530433556	chr9:17722125-17722126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563387414	chr9:17722127-17722128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370824493	chr9:17722135-17722136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs28399352	chr9:17722163-17722164	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs571653392	chr9:17722184-17722185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532678650	chr9:17722260-17722261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570844538	chr9:17722278-17722279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566275553	chr9:17722321-17722322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187664929	chr9:17722322-17722323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530209429	chr9:17722836-17722837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184598096	chr9:17722840-17722841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558799744	chr9:17722920-17722921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537378989	chr9:17722924-17722925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs367717889	chr9:17722929-17722930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76255742	chr9:17722951-17722952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189512666	chr9:17722974-17722975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534280321	chr9:17722975-17722976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146303972	chr9:17723009-17723010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs3808690	chr9:17723015-17723016	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs572277179	chr9:17723151-17723152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183287286	chr9:17725604-17725605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368582614	chr9:17725613-17725614	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Renal cell carcinoma	21215367	CNVD
Ovarian cancer	19835627	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:962 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17720800-17721200	Enhancers	H9 Cell Line	embryonic stem cell
2	chr9:17721000-17721200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr9:17721800-17722400	Enhancers	Dnd41	blood
4	chr9:17722800-17723200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr9:17725600-17726400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:17725800-17726800	Enhancers	Liver	Liver
7	chr9:17726600-17726800	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr9:17727000-17727400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr9:17735600-17736400	Enhancers	Fetal Brain Male	brain
10	chr9:17736400-17737600	Weak transcription	Fetal Brain Male	brain
11	chr9:17737600-17737800	Enhancers	Fetal Brain Male	brain
12	chr9:17737800-17738400	Weak transcription	Fetal Brain Male	brain
13	chr9:17738400-17740000	Enhancers	Fetal Brain Male	brain
14	chr9:17739200-17741800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr9:17741200-17742400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr9:17741600-17742200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr9:17741800-17742200	Enhancers	H9 Cell Line	embryonic stem cell
18	chr9:17741800-17742200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr9:17741800-17742200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr9:17741800-17742400	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr9:17741800-17742600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr9:17741800-17742600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr9:17742200-17742400	Enhancers	Gastric	stomach
24	chr9:17742400-17742800	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr9:17742800-17743000	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr9:17743000-17743800	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr9:17743800-17744000	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr9:17744000-17750200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr9:17744800-17745000	Enhancers	Gastric	stomach
30	chr9:17749400-17750200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr9:17750000-17750800	Enhancers	Brain Germinal Matrix	brain
32	chr9:17750200-17750800	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr9:17750800-17751800	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr9:17752000-17752200	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr9:17754800-17772600	Weak transcription	Hela-S3	cervix
36	chr9:17757400-17757800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:17757800-17758000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr9:17762400-17764800	Weak transcription	Brain Cingulate Gyrus	brain
39	chr9:17764200-17764800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr9:17764400-17764600	Enhancers	Gastric	stomach
41	chr9:17764600-17782800	Weak transcription	Gastric	stomach
42	chr9:17764800-17765200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr9:17765200-17766200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr9:17765600-17766000	Enhancers	Fetal Muscle Trunk	muscle
45	chr9:17765600-17766200	Enhancers	NHDF-Ad	bronchial
46	chr9:17766000-17766200	Enhancers	Fetal Brain Male	brain
47	chr9:17769000-17769400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr9:17771400-17771800	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr9:17775800-17776800	Enhancers	Fetal Brain Male	brain
50	chr9:17776000-17776400	Weak transcription	Brain Inferior Temporal Lobe	brain

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