Variant report

Variant	nsv892226
Chromosome Location	chr9:8435525-8522326
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	CEBPB	chr9:8467531-8467731	HepG2	liver:	n/a	chr9:8467626-8467637 chr9:8467628-8467637 chr9:8467628-8467639
2	CEBPB	chr9:8489844-8490104	K562	blood:	n/a	chr9:8489990-8490003 chr9:8489992-8490001 chr9:8489990-8490003 chr9:8489992-8490001 chr9:8489991-8490002 chr9:8489992-8490001 chr9:8489990-8490001 chr9:8489992-8490001
3	CEBPB	chr9:8477541-8477760	HepG2	liver:	n/a	chr9:8477663-8477674
4	CEBPB	chr9:8477551-8477752	H1-hESC	embryonic stem cell:	n/a	chr9:8477663-8477674
5	CEBPB	chr9:8438508-8438534	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr9:8460586-8460837	A549	lung:	n/a	chr9:8460683-8460694 chr9:8460682-8460695
7	CEBPB	chr9:8489831-8490143	A549	lung:	n/a	chr9:8489990-8490003 chr9:8489992-8490001 chr9:8489990-8490003 chr9:8489992-8490001 chr9:8489991-8490002 chr9:8489992-8490001 chr9:8489990-8490001 chr9:8489992-8490001
8	CEBPB	chr9:8489836-8490146	Hela-S3	cervix:	n/a	chr9:8489990-8490003 chr9:8489992-8490001 chr9:8489990-8490003 chr9:8489992-8490001 chr9:8489991-8490002 chr9:8489992-8490001 chr9:8489990-8490001 chr9:8489992-8490001
9	CEBPB	chr9:8489834-8490183	H1-hESC	embryonic stem cell:	n/a	chr9:8489990-8490003 chr9:8489992-8490001 chr9:8489990-8490003 chr9:8489992-8490001 chr9:8489991-8490002 chr9:8489992-8490001 chr9:8489990-8490001 chr9:8489992-8490001
10	CEBPB	chr9:8460542-8460750	HepG2	liver:	n/a	chr9:8460683-8460694 chr9:8460682-8460695
11	CEBPB	chr9:8464964-8465374	IMR90	lung:	n/a	chr9:8465304-8465317 chr9:8465304-8465315 chr9:8465304-8465317 chr9:8465088-8465099
12	CEBPB	chr9:8464933-8465436	HepG2	liver:	n/a	chr9:8465304-8465317 chr9:8465304-8465315 chr9:8465304-8465317 chr9:8465088-8465099
13	CEBPB	chr9:8492380-8492642	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr9:8489832-8490170	HepG2	liver:	n/a	chr9:8489990-8490003 chr9:8489992-8490001 chr9:8489990-8490003 chr9:8489992-8490001 chr9:8489991-8490002 chr9:8489992-8490001 chr9:8489990-8490001 chr9:8489992-8490001
15	CEBPB	chr9:8460568-8460828	IMR90	lung:	n/a	chr9:8460683-8460694 chr9:8460682-8460695
16	CEBPB	chr9:8467536-8467652	H1-hESC	embryonic stem cell:	n/a	chr9:8467626-8467637 chr9:8467628-8467637 chr9:8467628-8467639
17	CEBPB	chr9:8464990-8465383	A549	lung:	n/a	chr9:8465304-8465317 chr9:8465304-8465315 chr9:8465304-8465317 chr9:8465088-8465099
18	CEBPB	chr9:8467577-8467643	K562	blood:	n/a	chr9:8467626-8467637 chr9:8467628-8467637 chr9:8467628-8467639
19	CHD2	chr9:8514763-8515040	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr9:8486260-8486410	AoAF	blood vessel:	n/a	n/a
21	CTCF	chr9:8486247-8486350	GM12891	blood:	n/a	n/a
22	CTCF	chr9:8514840-8514990	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr9:8486160-8486310	Caco-2	colon:	n/a	n/a
24	CTCF	chr9:8495020-8495170	NHEK	skin:	n/a	n/a
25	CTCF	chr9:8486220-8486370	SAEC	small airway:	n/a	n/a
26	CTCF	chr9:8486220-8486370	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr9:8486200-8486350	HPF	lung:	n/a	n/a
28	CTCF	chr9:8486180-8486330	BE2_C	brain:	n/a	n/a
29	CTCF	chr9:8514840-8514990	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr9:8514980-8515130	BE2_C	brain:	n/a	n/a
31	CTCF	chr9:8486242-8486333	GM12878	blood:	n/a	n/a
32	CTCF	chr9:8486200-8486350	GM12873	blood:	n/a	n/a
33	CTCF	chr9:8486180-8486330	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr9:8486360-8486510	HFF	foreskin:	n/a	n/a
35	CTCF	chr9:8514860-8515010	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr9:8486200-8486350	HMF	breast:	n/a	n/a
37	CTCF	chr9:8486020-8486170	AG09309	skin:	n/a	n/a
38	CTCF	chr9:8486140-8486290	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr9:8486247-8486317	MCF-7	breast:	n/a	n/a
40	CTCF	chr9:8486227-8486308	LNCaP	prostate:	n/a	n/a
41	CTCF	chr9:8514860-8515010	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr9:8486291-8486320	HepG2	liver:	n/a	n/a
43	CTCF	chr9:8514900-8515050	HepG2	liver:	n/a	n/a
44	CTCF	chr9:8504217-8504307	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr9:8479124-8479177	GM13976	blood:	n/a	n/a
46	CTCF	chr9:8486260-8486410	HCM	heart:	n/a	n/a
47	CTCF	chr9:8514880-8515030	HCM	heart:	n/a	n/a
48	CTCF	chr9:8486166-8486372	Medullo	brain:	n/a	n/a
49	CTCF	chr9:8514920-8515070	NB4	blood:	n/a	n/a
50	CTCF	chr9:8486160-8486310	AG09319	gingival:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:8454918-8454968	SK-N-SH	brain:	n/a
2	chr9:8454918-8454968	IMR90	lung:	fetal
3	chr9:8454918-8454968	HUVEC	blood vessel:	n/a
4	chr9:8454918-8454968	HEEpiC	esophagus:	n/a
5	chr9:8454918-8454968	NHDF-neo	bronchial:	n/a
6	chr9:8454918-8454968	BE2_C	brain:	n/a
7	chr9:8454918-8454968	HRCEpiC	kidney:	n/a
8	chr9:8454918-8454968	CMK	blood:	n/a
9	chr9:8454918-8454968	Hela-S3	cervix:	n/a
10	chr9:8454918-8454968	HIPEpiC	eye:	n/a
11	chr9:8454918-8454968	BJ	skin:	n/a
12	chr9:8454918-8454968	ECC-1	luminal epithelium:	n/a
13	chr9:8454918-8454968	NT2-D1	testis:	n/a
14	chr9:8454918-8454968	GM12878	blood:	n/a
15	chr9:8454918-8454968	AG04450	lung:	fetal
16	chr9:8454918-8454968	NHBE	bronchial:	n/a
17	chr9:8454918-8454968	GM06990	blood:	n/a
18	chr9:8454918-8454968	HepG2	liver:	n/a
19	chr9:8454918-8454968	AG10803	skin:	n/a
20	chr9:8454918-8454968	HMEC	breast:	n/a
21	chr9:8454918-8454968	RPTEC	kidney:	n/a
22	chr9:8454918-8454968	ovcar-3	ovarian:	n/a
23	chr9:8454918-8454968	SK-N-MC	brain:	n/a
24	chr9:8454918-8454968	PANC-1	pancreas:	n/a
25	chr9:8454918-8454968	PFSK-1	brain:	n/a
26	chr9:8454918-8454968	MCF-7	breast:	n/a
27	chr9:8454918-8454968	AoSMC	blood vessel:	n/a
28	chr9:8454918-8454968	HNPCEpiC	eye:	n/a
29	chr9:8454918-8454968	K562	blood:	n/a
30	chr9:8454918-8454968	H1-hESC	embryonic stem cell:	embryo
31	chr9:8454918-8454968	GM12891	blood:	n/a
32	chr9:8454918-8454968	NH-A	brain:	n/a
33	chr9:8454918-8454968	AG04449	skin:	fetal
34	chr9:8454918-8454968	HAEpiC	amniotic membrane:	n/a
35	chr9:8454918-8454968	U87	brain:	n/a
36	chr9:8454918-8454968	HRPEpiC	eye:	n/a
37	chr9:8454918-8454968	GM19239	blood:	n/a
38	chr9:8454918-8454968	AG09319	gingival:	n/a
39	chr9:8454918-8454968	GM12892	blood:	n/a
40	chr9:8454918-8454968	LNCaP	prostate:	n/a
41	chr9:8454918-8454968	SAEC	small airway:	n/a
42	chr9:8454918-8454968	Caco-2	colon:	n/a
43	chr9:8454918-8454968	ProgFib	skin:	n/a
44	chr9:8454918-8454968	A549	lung:	n/a
45	chr9:8454918-8454968	T-47D	breast:	n/a
46	chr9:8454918-8454968	HCPEpiC	choroid plexus:	n/a
47	chr9:8454918-8454968	Hepatocyte	liver:	n/a
48	chr9:8454918-8454968	MCF10A-Er-Src	breast:	n/a
49	chr9:8454918-8454968	HCM	heart:	n/a
50	chr9:8454918-8454968	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:8435134..8437912-chr9:8440179..8442505,2	MCF-7	breast:
2	chr9:8495120..8497177-chr9:8504224..8507159,2	K562	blood:
3	chr9:8495120..8497177-chr9:8504224..8507159,2	K562	blood:
4	chr9:8435134..8437912-chr9:8440179..8442505,2	MCF-7	breast:

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

Extended variants
information (count: 4551 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:4551 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2890794	chr9:8435525-8435526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs561548422	chr9:8435566-8435567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141670751	chr9:8435581-8435582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548677845	chr9:8435585-8435586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144487563	chr9:8435586-8435587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148420419	chr9:8435587-8435588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552635923	chr9:8435593-8435594	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs16927865	chr9:8435594-8435595	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs141736571	chr9:8435682-8435683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201572325	chr9:8435698-8435699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144439068	chr9:8435699-8435700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374725171	chr9:8435700-8435701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567077584	chr9:8435701-8435702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10977098	chr9:8435702-8435703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370818223	chr9:8435729-8435730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs3043782	chr9:8435730-8435731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550452809	chr9:8435734-8435735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571214755	chr9:8435738-8435739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556995267	chr9:8435739-8435740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538197932	chr9:8435759-8435760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140650464	chr9:8435761-8435762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553854123	chr9:8435771-8435772	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77629513	chr9:8435828-8435829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144510615	chr9:8435853-8435854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs723628	chr9:8435887-8435888	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs185023185	chr9:8435922-8435923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10758974	chr9:8435925-8435926	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs575584811	chr9:8435953-8435954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368460983	chr9:8435954-8435955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs367858435	chr9:8435978-8435979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12350885	chr9:8435986-8435987	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs573473033	chr9:8436014-8436015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561799298	chr9:8436042-8436043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573800765	chr9:8436072-8436073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12352744	chr9:8436084-8436085	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs559481708	chr9:8436092-8436093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140695142	chr9:8436111-8436112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189645447	chr9:8436120-8436121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149762085	chr9:8436169-8436170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564478472	chr9:8436172-8436173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10815873	chr9:8436194-8436195	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs371084534	chr9:8436200-8436201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77018069	chr9:8436213-8436214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs80332687	chr9:8436215-8436216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181101824	chr9:8436239-8436240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10977099	chr9:8436261-8436262	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs145774092	chr9:8436263-8436264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529569677	chr9:8436297-8436298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10977100	chr9:8436311-8436312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111280210	chr9:8436344-8436345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	20668451	CNVD
Schizophrenia	20838587	CNVD
Glioblastoma	18772890	CNVD
Glioblastoma multiforme	21390271	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:649 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8389600-8451000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr9:8402600-8448800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr9:8402800-8438000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr9:8405800-8438000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr9:8410600-8436800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr9:8415400-8435800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr9:8418200-8476000	Weak transcription	Fetal Brain Male	brain
8	chr9:8419200-8491000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr9:8419800-8447600	Weak transcription	Fetal Brain Female	brain
10	chr9:8420200-8436800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:8420600-8466000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr9:8420600-8557600	Weak transcription	Aorta	Aorta
13	chr9:8421400-8456400	Weak transcription	Ovary	ovary
14	chr9:8422000-8464800	Weak transcription	Brain Germinal Matrix	brain
15	chr9:8423200-8446800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr9:8424200-8485000	Weak transcription	Fetal Kidney	kidney
17	chr9:8424600-8437800	Weak transcription	Fetal Heart	heart
18	chr9:8425600-8447600	Weak transcription	Fetal Muscle Leg	muscle
19	chr9:8428000-8447400	Weak transcription	Fetal Muscle Trunk	muscle
20	chr9:8430000-8436600	Weak transcription	Brain Cingulate Gyrus	brain
21	chr9:8430200-8465000	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr9:8431200-8436800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr9:8431400-8437000	Weak transcription	Brain Hippocampus Middle	brain
24	chr9:8431400-8438000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr9:8431400-8438200	Weak transcription	Brain Angular Gyrus	brain
26	chr9:8432000-8436800	Weak transcription	Brain Substantia Nigra	brain
27	chr9:8432600-8448400	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr9:8432800-8447400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr9:8433800-8442800	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr9:8434200-8485200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr9:8434400-8436800	Strong transcription	Fetal Lung	lung
32	chr9:8435800-8436200	Strong transcription	Brain Inferior Temporal Lobe	brain
33	chr9:8436200-8436800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr9:8436600-8437200	Enhancers	Brain Cingulate Gyrus	brain
35	chr9:8436800-8437000	Genic enhancers	Brain Inferior Temporal Lobe	brain
36	chr9:8436800-8438200	Enhancers	Brain Substantia Nigra	brain
37	chr9:8436800-8438800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr9:8436800-8439000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr9:8436800-8446600	Weak transcription	Fetal Lung	lung
40	chr9:8437000-8437600	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr9:8437000-8437800	Enhancers	Brain Hippocampus Middle	brain
42	chr9:8437000-8438400	Enhancers	Placenta Amnion	Placenta Amnion
43	chr9:8437200-8441200	Weak transcription	Brain Cingulate Gyrus	brain
44	chr9:8437600-8438200	Enhancers	Brain Anterior Caudate	brain
45	chr9:8437600-8438400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr9:8437600-8438400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr9:8437600-8439800	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr9:8437800-8438200	Enhancers	Fetal Heart	heart
49	chr9:8437800-8441600	Weak transcription	Brain Hippocampus Middle	brain
50	chr9:8438000-8438200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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