Variant report

Variant	nsv466271
Chromosome Location	chr9:17329964-17438391
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	chr9:17330165-17330444	IMR90	lung:	n/a	chr9:17330288-17330305
3	CEBPB	chr9:17437391-17437559	H1-hESC	embryonic stem cell:	n/a	chr9:17437440-17437453 chr9:17437442-17437451 chr9:17437442-17437451 chr9:17437440-17437453 chr9:17437442-17437453 chr9:17437442-17437451 chr9:17437442-17437453 chr9:17437440-17437453 chr9:17437442-17437451
4	CEBPB	chr9:17406868-17407046	HepG2	liver:	n/a	chr9:17406919-17406930 chr9:17406918-17406931
5	CEBPB	chr9:17423031-17423372	IMR90	lung:	n/a	n/a
6	CEBPB	chr9:17377365-17377657	Hela-S3	cervix:	n/a	chr9:17377489-17377500
7	CEBPB	chr9:17377335-17377654	HepG2	liver:	n/a	chr9:17377489-17377500
8	CEBPB	chr9:17397451-17397769	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr9:17437376-17437608	A549	lung:	n/a	chr9:17437440-17437453 chr9:17437442-17437451 chr9:17437442-17437451 chr9:17437440-17437453 chr9:17437442-17437453 chr9:17437442-17437451 chr9:17437442-17437453 chr9:17437440-17437453 chr9:17437442-17437451
10	CEBPB	chr9:17419882-17420104	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr9:17377353-17377652	H1-hESC	embryonic stem cell:	n/a	chr9:17377489-17377500
12	CEBPB	chr9:17398373-17398650	IMR90	lung:	n/a	n/a
13	CEBPB	chr9:17398398-17398610	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr9:17377409-17377627	A549	lung:	n/a	chr9:17377489-17377500
15	CEBPB	chr9:17377270-17377684	A549	lung:	n/a	chr9:17377489-17377500
16	CEBPB	chr9:17342487-17342694	HepG2	liver:	n/a	chr9:17342605-17342616 chr9:17342604-17342617 chr9:17342604-17342615 chr9:17342604-17342617 chr9:17342604-17342617
17	CEBPB	chr9:17406822-17407056	A549	lung:	n/a	chr9:17406919-17406930 chr9:17406918-17406931
18	CEBPB	chr9:17397502-17397682	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:17359924-17360128	HepG2	liver:	n/a	chr9:17360064-17360075 chr9:17360018-17360029
20	CEBPB	chr9:17377353-17377651	IMR90	lung:	n/a	chr9:17377489-17377500
21	CEBPB	chr9:17342525-17342788	IMR90	lung:	n/a	chr9:17342605-17342616 chr9:17342604-17342617 chr9:17342604-17342615 chr9:17342604-17342617 chr9:17342604-17342617
22	CEBPB	chr9:17346553-17346642	HepG2	liver:	n/a	n/a
23	CEBPB	chr9:17406793-17407054	IMR90	lung:	n/a	chr9:17406919-17406930 chr9:17406918-17406931
24	CEBPB	chr9:17377317-17377640	A549	lung:	n/a	chr9:17377489-17377500
25	CHD1	chr9:17396955-17397053	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr9:17402260-17402410	A549	lung:	n/a	n/a
27	CTCF	chr9:17402420-17402570	BE2_C	brain:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
28	CTCF	chr9:17402760-17402910	HFF	foreskin:	n/a	n/a
29	CTCF	chr9:17402440-17402590	HMF	breast:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
30	CTCF	chr9:17402460-17402610	HA-sp	spinal cord:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
31	CTCF	chr9:17402420-17402570	HA-sp	spinal cord:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
32	CTCF	chr9:17402460-17402610	HMF	breast:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
33	CTCF	chr9:17402440-17402590	NHEK	skin:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
34	CTCF	chr9:17402520-17402670	HAc	cerebellar:	n/a	n/a
35	CTCF	chr9:17367260-17367410	GM12867	blood:	n/a	n/a
36	CTCF	chr9:17402520-17402670	MCF-7	breast:	n/a	n/a
37	CTCF	chr9:17402438-17402548	LNCaP	prostate:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
38	CTCF	chr9:17353658-17353729	GM13976	blood:	n/a	n/a
39	CTCF	chr9:17347937-17347982	GM13976	blood:	n/a	n/a
40	CTCF	chr9:17402733-17402821	MCF-7	breast:	n/a	n/a
41	CTCF	chr9:17402259-17402864	H1-hESC	embryonic stem cell:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
42	CTCF	chr9:17367868-17367872	Fibrobl	skin:	n/a	n/a
43	CTCF	chr9:17402780-17402930	NHLF	lung:	n/a	n/a
44	CTCF	chr9:17402420-17402570	HCPEpiC	choroid plexus:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
45	CTCF	chr9:17402460-17402610	AG04449	skin:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
46	CTCF	chr9:17402460-17402610	HCPEpiC	choroid plexus:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
47	CTCF	chr9:17402480-17402630	HFF	foreskin:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
48	CTCF	chr9:17402400-17402550	HRPEpiC	eye:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
49	CTCF	chr9:17402340-17402490	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr9:17402440-17402590	HUVEC	blood vessel:	n/a	chr9:17402495-17402516 chr9:17402500-17402518

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17354129-17354179	NT2-D1	testis:	n/a
2	chr9:17354129-17354179	NT2-D1	testis:	n/a
3	chr9:17354129-17354179	AG09319	gingival:	n/a
4	chr9:17354129-17354179	U87	brain:	n/a
5	chr9:17354129-17354179	Hela-S3	cervix:	n/a
6	chr9:17354129-17354179	Hepatocyte	liver:	n/a
7	chr9:17354129-17354179	HCT-116	colon:	n/a
8	chr9:17354129-17354179	SAEC	small airway:	n/a
9	chr9:17354129-17354179	HL-60	blood:	n/a
10	chr9:17354129-17354179	HRCEpiC	kidney:	n/a
11	chr9:17354129-17354179	HMEC	breast:	n/a
12	chr9:17354129-17354179	Caco-2	colon:	n/a
13	chr9:17354129-17354179	SK-N-SH_RA	brain:	n/a
14	chr9:17354129-17354179	HCM	heart:	n/a
15	chr9:17354129-17354179	AG09309	skin:	n/a
16	chr9:17354129-17354179	HEEpiC	esophagus:	n/a
17	chr9:17354129-17354179	GM06990	blood:	n/a
18	chr9:17354129-17354179	HNPCEpiC	eye:	n/a
19	chr9:17354129-17354179	ovcar-3	ovarian:	n/a
20	chr9:17354129-17354179	CMK	blood:	n/a
21	chr9:17354129-17354179	GM19239	blood:	n/a
22	chr9:17354129-17354179	HCPEpiC	choroid plexus:	n/a
23	chr9:17354129-17354179	K562	blood:	n/a
24	chr9:17354129-17354179	HEK293	kidney:	embryo
25	chr9:17354129-17354179	HUVEC	blood vessel:	n/a
26	chr9:17354129-17354179	HepG2	liver:	n/a
27	chr9:17354129-17354179	ECC-1	luminal epithelium:	n/a
28	chr9:17354129-17354179	BJ	skin:	n/a
29	chr9:17354129-17354179	HAEpiC	amniotic membrane:	n/a
30	chr9:17354129-17354179	HCF	heart:	n/a
31	chr9:17354129-17354179	GM12892	blood:	n/a
32	chr9:17354129-17354179	AG10803	skin:	n/a
33	chr9:17354129-17354179	NH-A	brain:	n/a
34	chr9:17354129-17354179	SKMC	muscle:	n/a
35	chr9:17354129-17354179	AG04450	lung:	fetal
36	chr9:17354129-17354179	HPAEpiC	pulmonary alveolar:	n/a
37	chr9:17354129-17354179	PANC-1	pancreas:	n/a
38	chr9:17354129-17354179	H1-hESC	embryonic stem cell:	embryo
39	chr9:17354129-17354179	A549	lung:	n/a
40	chr9:17354129-17354179	NHDF-neo	bronchial:	n/a
41	chr9:17354129-17354179	GM12878	blood:	n/a
42	chr9:17354129-17354179	Jurkat	blood:	n/a
43	chr9:17354129-17354179	HIPEpiC	eye:	n/a
44	chr9:17354129-17354179	SK-N-MC	brain:	n/a
45	chr9:17354129-17354179	SK-N-SH	brain:	n/a
46	chr9:17354129-17354179	IMR90	lung:	fetal
47	chr9:17354129-17354179	MCF10A-Er-Src	breast:	n/a
48	chr9:17354129-17354179	NB4	blood:	n/a
49	chr9:17354129-17354179	PrEC	prostate:	n/a
50	chr9:17354129-17354179	LNCaP	prostate:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3GL2-2	chr9:17415964-17416187	NONHSAT130301
2	lnc-SH3GL2-2	chr9:17415816-17415879	NONHSAT130301
3	lnc-SH3GL2-1	chr9:17435732-17437445	NONHSAT130302

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

Extended variants
information (count: 4875 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:4875 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1442528	chr9:17329964-17329965	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562588831	chr9:17330007-17330008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533145833	chr9:17330013-17330014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551320137	chr9:17330026-17330027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536901623	chr9:17330059-17330060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10963038	chr9:17330091-17330092	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs546789579	chr9:17330180-17330181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568147975	chr9:17330201-17330202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112341081	chr9:17330242-17330243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140174669	chr9:17330268-17330269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557091623	chr9:17330295-17330296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575355065	chr9:17330297-17330298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539452788	chr9:17330361-17330362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144141295	chr9:17330369-17330370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573495017	chr9:17330412-17330413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144336745	chr9:17330419-17330420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562333889	chr9:17330426-17330427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77071787	chr9:17330435-17330436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111902410	chr9:17330478-17330479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs117873595	chr9:17330492-17330493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142304206	chr9:17330533-17330534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533907512	chr9:17330534-17330535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551774703	chr9:17330541-17330542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs3765040	chr9:17330558-17330559	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs528421534	chr9:17330561-17330562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181171154	chr9:17330584-17330585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568293470	chr9:17330593-17330594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535637824	chr9:17330604-17330605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550756460	chr9:17330609-17330610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369982294	chr9:17330614-17330615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201955741	chr9:17330617-17330618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186579124	chr9:17330665-17330666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376848122	chr9:17330702-17330703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539502626	chr9:17330714-17330715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371499380	chr9:17330726-17330727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201214080	chr9:17330730-17330731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369422192	chr9:17330734-17330735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200975303	chr9:17330759-17330760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200291548	chr9:17330764-17330765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150855410	chr9:17330770-17330771	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555774442	chr9:17330776-17330777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376731270	chr9:17330847-17330848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573955037	chr9:17330873-17330874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139238514	chr9:17330911-17330912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562715116	chr9:17330965-17330966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144189822	chr9:17330988-17330989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567474271	chr9:17331010-17331011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538100286	chr9:17331030-17331031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146556986	chr9:17331036-17331037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191336005	chr9:17331061-17331062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:706 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17262800-17339800	Weak transcription	Left Ventricle	heart
2	chr9:17284400-17344800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr9:17292200-17367200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:17294000-17334000	Weak transcription	Fetal Stomach	stomach
5	chr9:17294000-17346000	Weak transcription	Fetal Muscle Leg	muscle
6	chr9:17301200-17332200	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr9:17313400-17333200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr9:17315400-17347400	Weak transcription	Colon Smooth Muscle	Colon
9	chr9:17315400-17349800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr9:17318400-17334000	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr9:17319000-17349800	Weak transcription	Osteobl	bone
12	chr9:17319400-17349800	Weak transcription	NH-A	brain
13	chr9:17320600-17333800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr9:17321600-17331600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr9:17321600-17331600	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr9:17321600-17334600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr9:17321800-17340800	Weak transcription	HUVEC	blood vessel
18	chr9:17321800-17342800	Weak transcription	Pancreas	Pancrea
19	chr9:17323600-17342800	Weak transcription	Aorta	Aorta
20	chr9:17325800-17331400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr9:17327000-17349800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr9:17327800-17346200	Weak transcription	HSMM	muscle
23	chr9:17328600-17330000	Weak transcription	Fetal Lung	lung
24	chr9:17328600-17330600	Weak transcription	Liver	Liver
25	chr9:17328800-17341400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr9:17329200-17367000	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr9:17329800-17330200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr9:17329800-17330200	Enhancers	NHDF-Ad	bronchial
29	chr9:17330000-17330400	Enhancers	Fetal Lung	lung
30	chr9:17330200-17342600	Weak transcription	Ovary	ovary
31	chr9:17330200-17350200	Weak transcription	NHDF-Ad	bronchial
32	chr9:17330200-17367000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr9:17330400-17346000	Weak transcription	Fetal Lung	lung
34	chr9:17330600-17334800	Strong transcription	Liver	Liver
35	chr9:17330600-17350800	Weak transcription	Fetal Kidney	kidney
36	chr9:17331200-17343000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr9:17331400-17332800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr9:17331400-17333200	Weak transcription	Adipose Nuclei	Adipose
39	chr9:17331600-17332600	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr9:17331600-17333000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr9:17331600-17342800	Weak transcription	Dnd41	blood
42	chr9:17331800-17332400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr9:17331800-17332800	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr9:17332000-17332200	Enhancers	H1 Cell Line	embryonic stem cell
45	chr9:17332000-17332400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr9:17332000-17332800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr9:17332200-17335200	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr9:17332200-17346800	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr9:17332200-17367000	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr9:17332400-17332600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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