Variant report

Variant	nsv1015524
Chromosome Location	chr9:17350843-17419424
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	chr9:17396862-17396940	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr9:17377409-17377627	A549	lung:	n/a	chr9:17377489-17377500
3	CEBPB	chr9:17377270-17377684	A549	lung:	n/a	chr9:17377489-17377500
4	CEBPB	chr9:17398398-17398610	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr9:17406868-17407046	HepG2	liver:	n/a	chr9:17406919-17406930 chr9:17406918-17406931
6	CEBPB	chr9:17377317-17377640	A549	lung:	n/a	chr9:17377489-17377500
7	CEBPB	chr9:17377365-17377657	Hela-S3	cervix:	n/a	chr9:17377489-17377500
8	CEBPB	chr9:17406822-17407056	A549	lung:	n/a	chr9:17406919-17406930 chr9:17406918-17406931
9	CEBPB	chr9:17397502-17397682	IMR90	lung:	n/a	n/a
10	CEBPB	chr9:17377353-17377652	H1-hESC	embryonic stem cell:	n/a	chr9:17377489-17377500
11	CEBPB	chr9:17406793-17407054	IMR90	lung:	n/a	chr9:17406919-17406930 chr9:17406918-17406931
12	CEBPB	chr9:17377335-17377654	HepG2	liver:	n/a	chr9:17377489-17377500
13	CEBPB	chr9:17398373-17398650	IMR90	lung:	n/a	n/a
14	CEBPB	chr9:17377353-17377651	IMR90	lung:	n/a	chr9:17377489-17377500
15	CEBPB	chr9:17397451-17397769	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr9:17359924-17360128	HepG2	liver:	n/a	chr9:17360064-17360075 chr9:17360018-17360029
17	CHD1	chr9:17396955-17397053	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr9:17402440-17402590	NB4	blood:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
19	CTCF	chr9:17402420-17402570	AG04450	lung:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
20	CTCF	chr9:17403040-17403190	WI-38	lung:	n/a	n/a
21	CTCF	chr9:17402438-17402548	LNCaP	prostate:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
22	CTCF	chr9:17402311-17402608	A549	lung:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
23	CTCF	chr9:17402480-17402630	HFF-Myc	foreskin:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
24	CTCF	chr9:17402380-17402530	AG09319	gingival:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
25	CTCF	chr9:17402259-17402864	H1-hESC	embryonic stem cell:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
26	CTCF	chr9:17402460-17402610	AG04450	lung:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
27	CTCF	chr9:17402460-17402610	HA-sp	spinal cord:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
28	CTCF	chr9:17402400-17402550	AG09319	gingival:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
29	CTCF	chr9:17402321-17402692	IMR90	lung:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
30	CTCF	chr9:17402440-17402590	NHEK	skin:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
31	CTCF	chr9:17402440-17402590	HUVEC	blood vessel:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
32	CTCF	chr9:17402420-17402570	HVMF	connective:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
33	CTCF	chr9:17402420-17402570	NHDF-neo	bronchial:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
34	CTCF	chr9:17353658-17353729	GM13976	blood:	n/a	n/a
35	CTCF	chr9:17402262-17402688	HCT-116	colon:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
36	CTCF	chr9:17402620-17402770	AG09309	skin:	n/a	n/a
37	CTCF	chr9:17402500-17402650	HCM	heart:	n/a	chr9:17402500-17402518
38	CTCF	chr9:17402279-17402789	MCF-7	breast:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
39	CTCF	chr9:17354973-17355079	GM10248	blood:	n/a	n/a
40	CTCF	chr9:17402573-17402576	GM13977	blood:	n/a	n/a
41	CTCF	chr9:17402440-17402590	HMF	breast:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
42	CTCF	chr9:17402520-17402670	MCF-7	breast:	n/a	n/a
43	CTCF	chr9:17402385-17402625	HUVEC	blood vessel:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
44	CTCF	chr9:17411640-17411790	GM12873	blood:	n/a	n/a
45	CTCF	chr9:17402420-17402570	HCPEpiC	choroid plexus:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
46	CTCF	chr9:17402460-17402610	HPAF	blood vessel:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
47	CTCF	chr9:17402420-17402570	HA-sp	spinal cord:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
48	CTCF	chr9:17402420-17402570	HPF	lung:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
49	CTCF	chr9:17402460-17402610	HCPEpiC	choroid plexus:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
50	CTCF	chr9:17402380-17402530	Caco-2	colon:	n/a	chr9:17402495-17402516 chr9:17402500-17402518

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17354129-17354179	RPTEC	kidney:	n/a
2	chr9:17354129-17354179	T-47D	breast:	n/a
3	chr9:17354129-17354179	A549	lung:	n/a
4	chr9:17354129-17354179	HMEC	breast:	n/a
5	chr9:17354129-17354179	NB4	blood:	n/a
6	chr9:17354129-17354179	IMR90	lung:	fetal
7	chr9:17354129-17354179	HIPEpiC	eye:	n/a
8	chr9:17354129-17354179	HCM	heart:	n/a
9	chr9:17354129-17354179	HepG2	liver:	n/a
10	chr9:17354129-17354179	HEK293	kidney:	embryo
11	chr9:17354129-17354179	U87	brain:	n/a
12	chr9:17354129-17354179	CMK	blood:	n/a
13	chr9:17354129-17354179	HUVEC	blood vessel:	n/a
14	chr9:17354129-17354179	MCF-7	breast:	n/a
15	chr9:17354129-17354179	ovcar-3	ovarian:	n/a
16	chr9:17354129-17354179	AG04450	lung:	fetal
17	chr9:17354129-17354179	ProgFib	skin:	n/a
18	chr9:17354129-17354179	HPAEpiC	pulmonary alveolar:	n/a
19	chr9:17354129-17354179	PrEC	prostate:	n/a
20	chr9:17354129-17354179	NH-A	brain:	n/a
21	chr9:17354129-17354179	HRE	kidney:	n/a
22	chr9:17354129-17354179	AG10803	skin:	n/a
23	chr9:17354129-17354179	BJ	skin:	n/a
24	chr9:17354129-17354179	HEEpiC	esophagus:	n/a
25	chr9:17354129-17354179	AG09319	gingival:	n/a
26	chr9:17354129-17354179	PFSK-1	brain:	n/a
27	chr9:17354129-17354179	NT2-D1	testis:	n/a
28	chr9:17354129-17354179	SK-N-SH_RA	brain:	n/a
29	chr9:17354129-17354179	HL-60	blood:	n/a
30	chr9:17354129-17354179	Jurkat	blood:	n/a
31	chr9:17354129-17354179	Hepatocyte	liver:	n/a
32	chr9:17354129-17354179	ECC-1	luminal epithelium:	n/a
33	chr9:17354129-17354179	GM12891	blood:	n/a
34	chr9:17354129-17354179	HAEpiC	amniotic membrane:	n/a
35	chr9:17354129-17354179	HCF	heart:	n/a
36	chr9:17354129-17354179	AG09309	skin:	n/a
37	chr9:17354129-17354179	BE2_C	brain:	n/a
38	chr9:17354129-17354179	PANC-1	pancreas:	n/a
39	chr9:17354129-17354179	HCPEpiC	choroid plexus:	n/a
40	chr9:17354129-17354179	GM06990	blood:	n/a
41	chr9:17354129-17354179	GM12892	blood:	n/a
42	chr9:17354129-17354179	HRCEpiC	kidney:	n/a
43	chr9:17354129-17354179	HNPCEpiC	eye:	n/a
44	chr9:17354129-17354179	SKMC	muscle:	n/a
45	chr9:17354129-17354179	LNCaP	prostate:	n/a
46	chr9:17354129-17354179	AoSMC	blood vessel:	n/a
47	chr9:17354129-17354179	SK-N-MC	brain:	n/a
48	chr9:17354129-17354179	HCT-116	colon:	n/a
49	chr9:17354129-17354179	Hela-S3	cervix:	n/a
50	chr9:17354129-17354179	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:17219155..17220052-chr9:17401883..17402825,5	MCF-7	breast:
2	chr9:17116081..17117141-chr9:17402172..17402905,3	MCF-7	breast:
3	chr9:17219375..17219930-chr9:17402045..17403347,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3GL2-2	chr9:17415816-17415879	NONHSAT130301
2	lnc-SH3GL2-2	chr9:17415964-17416187	NONHSAT130301

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

Extended variants
information (count: 3164 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3164 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10124487	chr9:17350843-17350844	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183293227	chr9:17350881-17350882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs16935548	chr9:17350888-17350889	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs535609799	chr9:17350954-17350955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12001651	chr9:17350958-17350959	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs188270063	chr9:17350967-17350968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10124513	chr9:17350983-17350984	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs564489789	chr9:17350993-17350994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140930656	chr9:17351013-17351014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541314683	chr9:17351019-17351020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559338274	chr9:17351020-17351021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529916105	chr9:17351220-17351221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548377133	chr9:17351221-17351222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563402754	chr9:17351244-17351245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192228467	chr9:17351252-17351253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78175796	chr9:17351255-17351256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551826821	chr9:17351273-17351274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570426279	chr9:17351281-17351282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73424151	chr9:17351284-17351285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547284037	chr9:17351292-17351293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568623420	chr9:17351336-17351337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368745804	chr9:17351383-17351384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs557109368	chr9:17351387-17351388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570755517	chr9:17351404-17351405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114498151	chr9:17351451-17351452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554815747	chr9:17351455-17351456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372272302	chr9:17351478-17351479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539535236	chr9:17351510-17351511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs111283814	chr9:17351524-17351525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376661726	chr9:17351533-17351534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10963058	chr9:17351580-17351581	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187812029	chr9:17351616-17351617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574764041	chr9:17351617-17351618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542081127	chr9:17351627-17351628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563465014	chr9:17351652-17351653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144685563	chr9:17351653-17351654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577720439	chr9:17351666-17351667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545889777	chr9:17351671-17351672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375163632	chr9:17351679-17351680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6475143	chr9:17351711-17351712	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs192689015	chr9:17351764-17351765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184312820	chr9:17351780-17351781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147908852	chr9:17351786-17351787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189493055	chr9:17351855-17351856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550802062	chr9:17351996-17351997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6475144	chr9:17352005-17352006	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs539597566	chr9:17352042-17352043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs75181760	chr9:17352087-17352088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116335281	chr9:17352109-17352110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181098244	chr9:17352157-17352158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17292200-17367200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:17329200-17367000	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr9:17330200-17367000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:17332200-17367000	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr9:17332400-17354800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr9:17332400-17367600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr9:17332800-17367400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr9:17334400-17353800	Weak transcription	Fetal Stomach	stomach
9	chr9:17335000-17367000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr9:17336800-17367200	Weak transcription	Fetal Intestine Small	intestine
11	chr9:17338600-17361400	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr9:17338800-17371800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr9:17339400-17367000	Weak transcription	Stomach Smooth Muscle	stomach
14	chr9:17339400-17367200	Weak transcription	Gastric	stomach
15	chr9:17340400-17365600	Weak transcription	Left Ventricle	heart
16	chr9:17341000-17351400	Weak transcription	Rectal Smooth Muscle	rectum
17	chr9:17341200-17367600	Weak transcription	Spleen	Spleen
18	chr9:17341400-17367000	Weak transcription	Right Ventricle	heart
19	chr9:17341400-17369600	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr9:17343000-17366800	Weak transcription	Pancreas	Pancrea
21	chr9:17343000-17367000	Weak transcription	Aorta	Aorta
22	chr9:17343200-17367000	Weak transcription	Dnd41	blood
23	chr9:17343800-17367000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr9:17344000-17352600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr9:17344200-17361400	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr9:17344400-17368800	Weak transcription	A549	lung
27	chr9:17346400-17352600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr9:17346600-17360200	Weak transcription	Ovary	ovary
29	chr9:17346600-17367200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr9:17346600-17367200	Weak transcription	Fetal Muscle Leg	muscle
31	chr9:17346800-17352800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr9:17346800-17367000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr9:17346800-17367000	Weak transcription	Adipose Nuclei	Adipose
34	chr9:17347000-17354800	Weak transcription	Liver	Liver
35	chr9:17347000-17361400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr9:17347000-17367000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:17347200-17354800	Weak transcription	Primary hematopoietic stem cells	blood
38	chr9:17347400-17366800	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr9:17347400-17367000	Weak transcription	Fetal Lung	lung
40	chr9:17350200-17351400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr9:17350600-17367600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr9:17351400-17352000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr9:17352000-17352200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr9:17352200-17353800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr9:17352600-17353000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr9:17352600-17353800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr9:17352800-17353600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr9:17353000-17353800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr9:17353600-17354200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr9:17353800-17354400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin

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