Variant report

Variant	nsv522711
Chromosome Location	chr9:3480671-3500471
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:69)
CpG islands
(count:0)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:69 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr9:3492642-3492649	Spleen_OC	spleen:	n/a	n/a
2	CUX1	chr9:3484040-3484196	GM12878	blood:	n/a	n/a
3	EP300	chr9:3498812-3498830	GM12878	blood:	n/a	n/a
4	EP300	chr9:3491596-3491629	GM12878	blood:	n/a	chr9:3491605-3491619
5	EP300	chr9:3497296-3497869	SK-N-SH	brain:	n/a	chr9:3497322-3497332 chr9:3497408-3497422
6	FAM48A	chr9:3481457-3481483	GM12878	blood:	n/a	n/a
7	FOS	chr9:3497436-3497764	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr9:3497382-3497806	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr9:3497380-3497663	HUVEC	blood vessel:	n/a	n/a
10	FOXA1	chr9:3490956-3491337	T-47D	breast:	n/a	chr9:3491148-3491163
11	FOXA1	chr9:3491036-3491359	HepG2	liver:	n/a	chr9:3491148-3491163
12	FOXA1	chr9:3491041-3491316	HepG2	liver:	n/a	chr9:3491148-3491163
13	FOXA2	chr9:3491029-3491301	HepG2	liver:	n/a	n/a
14	GATA2	chr9:3497466-3497756	HUVEC	blood vessel:	n/a	chr9:3497586-3497593
15	GATA3	chr9:3496704-3498073	SK-N-SH	brain:	n/a	chr9:3497586-3497593
16	GATA3	chr9:3496843-3496904	SH-SY5Y	brain:	n/a	n/a
17	GATA3	chr9:3491040-3491299	T-47D	breast:	n/a	n/a
18	GATA3	chr9:3497319-3498000	SK-N-SH	brain:	n/a	chr9:3497586-3497593
19	GATA3	chr9:3490887-3491522	MCF-7	breast:	n/a	chr9:3491007-3491014
20	GATA3	chr9:3490914-3491396	T-47D	breast:	n/a	chr9:3491007-3491014
21	GTF2F1	chr9:3496939-3496968	H1-hESC	embryonic stem cell:	n/a	n/a
22	GTF2F1	chr9:3495693-3495802	H1-hESC	embryonic stem cell:	n/a	n/a
23	IRF1	chr9:3487450-3487454	K562	blood:	n/a	n/a
24	JUN	chr9:3497393-3497747	HUVEC	blood vessel:	n/a	n/a
25	MAFK	chr9:3480837-3481098	HepG2	liver:	n/a	n/a
26	MAFK	chr9:3497437-3497799	IMR90	lung:	n/a	chr9:3497715-3497729 chr9:3497716-3497727
27	MAFK	chr9:3495158-3495412	HepG2	liver:	n/a	n/a
28	MAX	chr9:3498751-3498923	H1-hESC	embryonic stem cell:	n/a	chr9:3498768-3498777
29	MAZ	chr9:3494104-3494295	HepG2	liver:	n/a	n/a
30	MXI1	chr9:3498756-3498946	K562	blood:	n/a	n/a
31	MXI1	chr9:3498759-3498937	GM12878	blood:	n/a	n/a
32	MXI1	chr9:3482258-3482340	GM12878	blood:	n/a	n/a
33	MXI1	chr9:3492269-3492359	HepG2	liver:	n/a	n/a
34	MYC	chr9:3489300-3489335	H1-hESC	embryonic stem cell:	n/a	n/a
35	NFIC	chr9:3479217-3480672	GM12878	blood:	n/a	n/a
36	PBX3	chr9:3497292-3497924	SK-N-SH	brain:	n/a	n/a
37	POLR2A	chr9:3494242-3494257	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr9:3495424-3495624	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr9:3496827-3497248	H1-neurons	neurons:	n/a	n/a
40	POLR2A	chr9:3482630-3482763	K562	blood:	n/a	n/a
41	POLR2A	chr9:3492621-3492943	K562	blood:	n/a	n/a
42	POLR2A	chr9:3485928-3486090	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr9:3490053-3490258	K562	blood:	n/a	n/a
44	POLR2A	chr9:3487026-3487189	K562	blood:	n/a	n/a
45	POLR2A	chr9:3483393-3483410	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr9:3496728-3497289	H1-neurons	neurons:	n/a	n/a
47	POLR2A	chr9:3492239-3492674	K562	blood:	n/a	n/a
48	POLR2A	chr9:3490233-3490259	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr9:3486636-3486729	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr9:3487903-3488066	K562	blood:	n/a	n/a

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:3498806..3500362-chr9:3527236..3529774,2	K562	blood:
2	chr9:3478923..3481537-chr9:3524337..3526099,2	K562	blood:
3	chr9:3481303..3484512-chr9:3524609..3529415,5	MCF-7	breast:
4	chr9:3500140..3503117-chr9:3505256..3509401,4	K562	blood:
5	chr9:3493140..3494788-chr9:3496837..3499206,2	K562	blood:
6	chr9:3478739..3481374-chr9:3498869..3500820,2	MCF-7	breast:
7	chr9:3460990..3463630-chr9:3491395..3493289,2	K562	blood:
8	chr9:3493140..3494788-chr9:3496837..3499206,2	K562	blood:
9	chr9:3479015..3481934-chr9:3484671..3486572,2	K562	blood:
10	chr9:3488422..3492745-chr9:3526119..3529756,3	K562	blood:
11	chr9:3486226..3487734-chr9:3489487..3491455,2	K562	blood:
12	chr9:3491268..3494910-chr9:3525417..3527620,3	MCF-7	breast:
13	chr9:3486226..3487734-chr9:3489487..3491455,2	K562	blood:
14	chr9:3478739..3481374-chr9:3498869..3500820,2	MCF-7	breast:
15	chr9:3479015..3481934-chr9:3484671..3486572,2	K562	blood:
16	chr9:3498254..3500362-chr9:3527205..3528736,2	K562	blood:
17	chr9:3495106..3497016-chr9:3524367..3527205,3	MCF-7	breast:
18	chr9:3495458..3497256-chr9:3517334..3519565,2	K562	blood:
19	chr9:3489811..3492188-chr9:3524629..3527115,2	MCF-7	breast:
20	chr9:3489743..3491847-chr9:3522486..3524735,2	K562	blood:
21	chr9:3497780..3499700-chr9:3524560..3526876,2	K562	blood:
22	chr9:3477335..3480982-chr9:3525320..3527937,6	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNV2-8	chr9:3479874-3481237	NONHSAT130020

No data

Variant related genes	Relation type
RFX3	TF binding region
ENSG00000232104	chromatin interactions
ENSG00000080298	chromatin interactions

Extended variants
information (count: 787 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:787 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12238307	chr9:3480671-3480672	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554523645	chr9:3480673-3480674	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs568281347	chr9:3480693-3480694	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs117427773	chr9:3480694-3480695	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs556817284	chr9:3480725-3480726	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs73387740	chr9:3480735-3480736	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs145572023	chr9:3480740-3480741	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs558782728	chr9:3480758-3480759	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs572473676	chr9:3480784-3480785	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs541080874	chr9:3480791-3480792	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs561367292	chr9:3480824-3480825	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs200633246	chr9:3480833-3480834	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs373584156	chr9:3480834-3480835	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs202033631	chr9:3480837-3480838	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs376375453	chr9:3480857-3480858	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs371799485	chr9:3480861-3480862	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs190338106	chr9:3480876-3480877	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs183242901	chr9:3480894-3480895	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs532763086	chr9:3480908-3480909	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs552693230	chr9:3481029-3481030	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs559206296	chr9:3481052-3481053	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs186446362	chr9:3481092-3481093	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs192253010	chr9:3481153-3481154	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs7858455	chr9:3481194-3481195	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs536649862	chr9:3481286-3481287	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs78432383	chr9:3481333-3481334	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs77264874	chr9:3481378-3481379	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs559006720	chr9:3481481-3481482	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs2050955	chr9:3481486-3481487	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs7027858	chr9:3481487-3481488	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs7027859	chr9:3481488-3481489	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs535147075	chr9:3481489-3481490	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs192752285	chr9:3481514-3481515	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561424667	chr9:3481531-3481532	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs543798812	chr9:3481534-3481535	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs563974553	chr9:3481633-3481634	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs182559887	chr9:3481645-3481646	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs142466193	chr9:3481672-3481673	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs559932572	chr9:3481692-3481693	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs528657756	chr9:3481721-3481722	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs548314650	chr9:3481763-3481764	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs575793108	chr9:3481800-3481801	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs538369203	chr9:3481823-3481824	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs561442102	chr9:3481855-3481856	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs557189971	chr9:3481864-3481865	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs147275253	chr9:3481865-3481866	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs373189527	chr9:3481872-3481873	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs573821108	chr9:3481882-3481883	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs530436068	chr9:3481883-3481884	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs187551305	chr9:3481892-3481893	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Gastric cancer	16715143	CNVD
Glioblastoma multiforme	22286061	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
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
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	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
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21373258	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Autism	20808228	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:320 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:3455000-3483000	Weak transcription	Fetal Thymus	thymus
2	chr9:3468000-3480800	Weak transcription	NHDF-Ad	bronchial
3	chr9:3468200-3482200	Weak transcription	A549	lung
4	chr9:3468600-3483800	Weak transcription	Brain Hippocampus Middle	brain
5	chr9:3468600-3484800	Weak transcription	Ovary	ovary
6	chr9:3468800-3496600	Weak transcription	HSMMtube	muscle
7	chr9:3469400-3495600	Weak transcription	Fetal Kidney	kidney
8	chr9:3473600-3496600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr9:3473800-3482200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr9:3474000-3493600	Weak transcription	Fetal Stomach	stomach
11	chr9:3474400-3490800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr9:3474400-3524400	Weak transcription	Thymus	Thymus
13	chr9:3474600-3486000	Weak transcription	Small Intestine	intestine
14	chr9:3475000-3492600	Weak transcription	Lung	lung
15	chr9:3475800-3481000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr9:3475800-3483400	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr9:3475800-3485600	Weak transcription	Spleen	Spleen
18	chr9:3476400-3480800	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr9:3477200-3480800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr9:3477200-3480800	Enhancers	Primary B cells from cord blood	blood
21	chr9:3477200-3481000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr9:3477400-3485400	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr9:3477600-3484400	Weak transcription	Fetal Muscle Trunk	muscle
24	chr9:3477600-3487000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr9:3477600-3495600	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr9:3477800-3481200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr9:3477800-3483400	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr9:3477800-3483600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr9:3477800-3486200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr9:3478000-3486000	Weak transcription	Liver	Liver
31	chr9:3478200-3480800	Enhancers	Primary B cells from peripheral blood	blood
32	chr9:3478200-3481200	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr9:3478200-3484400	Weak transcription	Brain Anterior Caudate	brain
34	chr9:3478200-3485200	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr9:3478200-3488000	Weak transcription	Fetal Intestine Large	intestine
36	chr9:3478400-3481000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr9:3478600-3481000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr9:3478800-3480800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr9:3478800-3482200	Weak transcription	Brain Angular Gyrus	brain
40	chr9:3478800-3485800	Weak transcription	Fetal Brain Female	brain
41	chr9:3478800-3485800	Weak transcription	Dnd41	blood
42	chr9:3479000-3480800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr9:3479000-3486200	Weak transcription	HepG2	liver
44	chr9:3479000-3498800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr9:3479200-3480800	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr9:3479200-3483000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr9:3479200-3483000	Weak transcription	Fetal Muscle Leg	muscle
48	chr9:3479200-3483600	Weak transcription	Brain Germinal Matrix	brain
49	chr9:3479200-3484200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr9:3479200-3491200	Weak transcription	Adipose Nuclei	Adipose

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