Variant report

Variant	nsv1054381
Chromosome Location	chr9:79450930-79500447
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:246)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:79497594-79498091	GM12878	blood:	n/a	n/a
2	BCL3	chr9:79497679-79498015	GM12878	blood:	n/a	n/a
3	CEBPB	chr9:79488025-79488333	A549	lung:	n/a	chr9:79488197-79488208
4	CEBPB	chr9:79485635-79485977	A549	lung:	n/a	chr9:79485810-79485821
5	CEBPB	chr9:79488014-79488369	IMR90	lung:	n/a	chr9:79488197-79488208
6	CEBPB	chr9:79481749-79482054	A549	lung:	n/a	n/a
7	CEBPB	chr9:79485749-79485876	H1-hESC	embryonic stem cell:	n/a	chr9:79485810-79485821
8	CEBPB	chr9:79480843-79481043	IMR90	lung:	n/a	n/a
9	CEBPB	chr9:79488071-79488276	HepG2	liver:	n/a	chr9:79488197-79488208
10	CEBPB	chr9:79485641-79485971	HepG2	liver:	n/a	chr9:79485810-79485821
11	CEBPB	chr9:79485642-79485860	IMR90	lung:	n/a	chr9:79485810-79485821
12	CEBPB	chr9:79488053-79488641	H1-hESC	embryonic stem cell:	n/a	chr9:79488197-79488208
13	CEBPB	chr9:79470870-79471076	HepG2	liver:	n/a	n/a
14	CEBPB	chr9:79488161-79488239	K562	blood:	n/a	chr9:79488197-79488208
15	CEBPB	chr9:79477681-79477858	A549	lung:	n/a	n/a
16	CEBPB	chr9:79481694-79482082	IMR90	lung:	n/a	n/a
17	CHD1	chr9:79488354-79488492	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr9:79481729-79481980	A549	lung:	n/a	n/a
19	CTCF	chr9:79492900-79493050	A549	lung:	n/a	n/a
20	CTCF	chr9:79488380-79488530	AG04449	skin:	n/a	n/a
21	CTCF	chr9:79488420-79488570	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr9:79488400-79488550	HCFaa	heart:	n/a	n/a
23	CTCF	chr9:79488420-79488570	AG04449	skin:	n/a	n/a
24	CTCF	chr9:79488400-79488550	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr9:79488360-79488510	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr9:79488346-79488548	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr9:79488440-79488590	AG09319	gingival:	n/a	n/a
28	CTCF	chr9:79492720-79492870	HEK293	kidney:	n/a	n/a
29	CTCF	chr9:79488437-79488509	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr9:79488360-79488510	BJ	skin:	n/a	n/a
31	CTCF	chr9:79488380-79488530	BE2_C	brain:	n/a	n/a
32	CTCF	chr9:79488380-79488530	HMF	breast:	n/a	n/a
33	CTCF	chr9:79488360-79488510	AG10803	skin:	n/a	n/a
34	CTCF	chr9:79488340-79488490	AG09309	skin:	n/a	n/a
35	CTCF	chr9:79488380-79488530	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr9:79488400-79488550	AG09319	gingival:	n/a	n/a
37	CTCF	chr9:79488400-79488550	AG10803	skin:	n/a	n/a
38	CTCF	chr9:79488380-79488530	HAc	cerebellar:	n/a	n/a
39	CTCF	chr9:79488300-79488450	HFF	foreskin:	n/a	n/a
40	CTCF	chr9:79488380-79488530	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr9:79488400-79488550	BJ	skin:	n/a	n/a
42	CTCF	chr9:79488420-79488570	BE2_C	brain:	n/a	n/a
43	CTCF	chr9:79488400-79488550	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr9:79492740-79492890	HRE	kidney:	n/a	n/a
45	CTCF	chr9:79488400-79488550	HMF	breast:	n/a	n/a
46	CTCF	chr9:79492900-79493050	GM12874	blood:	n/a	n/a
47	CTCF	chr9:79488240-79488390	HCM	heart:	n/a	n/a
48	CTCF	chr9:79488400-79488550	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr9:79489120-79489270	BE2_C	brain:	n/a	n/a
50	CTCF	chr9:79492740-79492890	GM12871	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:79493927-79493977	MCF10A-Er-Src	breast:	n/a
2	chr9:79499202-79499252	PFSK-1	brain:	n/a
3	chr9:79499202-79499252	NT2-D1	testis:	n/a
4	chr9:79493927-79493977	IMR90	lung:	fetal
5	chr9:79493927-79493977	HL-60	blood:	n/a
6	chr9:79499202-79499252	Hepatocyte	liver:	n/a
7	chr9:79488657-79488707	NB4	blood:	n/a
8	chr9:79499202-79499252	HEK293	kidney:	embryo
9	chr9:79493927-79493977	Hela-S3	cervix:	n/a
10	chr9:79488657-79488707	HCPEpiC	choroid plexus:	n/a
11	chr9:79493927-79493977	K562	blood:	n/a
12	chr9:79488657-79488707	ECC-1	luminal epithelium:	n/a
13	chr9:79493927-79493977	HCM	heart:	n/a
14	chr9:79499202-79499252	GM12891	blood:	n/a
15	chr9:79493927-79493977	PrEC	prostate:	n/a
16	chr9:79488657-79488707	RPTEC	kidney:	n/a
17	chr9:79493927-79493977	BJ	skin:	n/a
18	chr9:79493927-79493977	Hepatocyte	liver:	n/a
19	chr9:79493927-79493977	HRCEpiC	kidney:	n/a
20	chr9:79499202-79499252	T-47D	breast:	n/a
21	chr9:79488657-79488707	AG04450	lung:	fetal
22	chr9:79488657-79488707	HEK293	kidney:	embryo
23	chr9:79488657-79488707	NT2-D1	testis:	n/a
24	chr9:79499202-79499252	MCF-7	breast:	n/a
25	chr9:79493927-79493977	HepG2	liver:	n/a
26	chr9:79499202-79499252	RPTEC	kidney:	n/a
27	chr9:79499202-79499252	NH-A	brain:	n/a
28	chr9:79499202-79499252	AG09319	gingival:	n/a
29	chr9:79499202-79499252	NHDF-neo	bronchial:	n/a
30	chr9:79488657-79488707	ovcar-3	ovarian:	n/a
31	chr9:79499202-79499252	CMK	blood:	n/a
32	chr9:79499202-79499252	HEEpiC	esophagus:	n/a
33	chr9:79493927-79493977	PFSK-1	brain:	n/a
34	chr9:79499202-79499252	HPAEpiC	pulmonary alveolar:	n/a
35	chr9:79488657-79488707	SK-N-SH_RA	brain:	n/a
36	chr9:79499202-79499252	BJ	skin:	n/a
37	chr9:79499202-79499252	HAEpiC	amniotic membrane:	n/a
38	chr9:79493927-79493977	NT2-D1	testis:	n/a
39	chr9:79488657-79488707	HCF	heart:	n/a
40	chr9:79499202-79499252	K562	blood:	n/a
41	chr9:79493927-79493977	ovcar-3	ovarian:	n/a
42	chr9:79493927-79493977	HIPEpiC	eye:	n/a
43	chr9:79488657-79488707	SAEC	small airway:	n/a
44	chr9:79493927-79493977	ProgFib	skin:	n/a
45	chr9:79499202-79499252	GM12892	blood:	n/a
46	chr9:79493927-79493977	GM12892	blood:	n/a
47	chr9:79499202-79499252	AG04450	lung:	fetal
48	chr9:79488657-79488707	LNCaP	prostate:	n/a
49	chr9:79499202-79499252	GM06990	blood:	n/a
50	chr9:79493927-79493977	T-47D	breast:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:79448266..79451222-chr9:79453871..79455788,2	MCF-7	breast:
2	chr9:79472515..79478078-chr9:79478521..79482952,4	MCF-7	breast:
3	chr9:79463198..79464986-chr9:79466037..79468315,2	MCF-7	breast:
4	chr9:79463198..79464986-chr9:79466037..79468315,2	MCF-7	breast:
5	chr9:79448266..79451222-chr9:79453871..79455788,2	MCF-7	breast:
6	chr9:79472515..79478078-chr9:79478521..79482952,4	MCF-7	breast:
7	chr9:79487218..79489827-chr9:79491730..79493342,2	MCF-7	breast:
8	chr9:79487218..79489827-chr9:79491730..79493342,2	MCF-7	breast:

No data

Variant related genes	Relation type
PRUNE2	TF binding region
PRUNE2	CpG island

Extended variants
information (count: 2068 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2068 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2000289	chr9:79450930-79450931	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189722976	chr9:79451022-79451023	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs564744255	chr9:79451046-79451047	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs2000288	chr9:79451050-79451051	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs149897231	chr9:79451062-79451063	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs192927825	chr9:79451063-79451064	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs541591487	chr9:79451110-79451111	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs542700810	chr9:79451127-79451128	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs562376169	chr9:79451180-79451181	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs35045046	chr9:79451182-79451183	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs116707232	chr9:79451188-79451189	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs114627387	chr9:79451214-79451215	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377315481	chr9:79451230-79451231	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527290337	chr9:79451251-79451252	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547124883	chr9:79451253-79451254	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185459722	chr9:79451296-79451297	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144948479	chr9:79451337-79451338	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556271342	chr9:79451395-79451396	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7855857	chr9:79451397-79451398	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs538405761	chr9:79451462-79451463	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148601100	chr9:79451508-79451509	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189982840	chr9:79451509-79451510	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11145093	chr9:79451522-79451523	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs182505268	chr9:79451524-79451525	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370477744	chr9:79451545-79451546	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542741967	chr9:79451546-79451547	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563184464	chr9:79451645-79451646	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184860158	chr9:79451659-79451660	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531418656	chr9:79451663-79451664	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574875740	chr9:79451675-79451676	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188351623	chr9:79451683-79451684	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565188062	chr9:79451703-79451704	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527629394	chr9:79451717-79451718	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2377810	chr9:79451734-79451735	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555954578	chr9:79451746-79451747	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs180764442	chr9:79451750-79451751	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560297160	chr9:79451762-79451763	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529684652	chr9:79451771-79451772	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10869838	chr9:79451775-79451776	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs372712870	chr9:79451825-79451826	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569725065	chr9:79451842-79451843	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs185715608	chr9:79451848-79451849	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142054846	chr9:79451849-79451850	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191261566	chr9:79451877-79451878	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534261959	chr9:79451929-79451930	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554425993	chr9:79451949-79451950	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573720669	chr9:79452018-79452019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs34876471	chr9:79452060-79452061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs149490939	chr9:79452061-79452062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542579363	chr9:79452076-79452077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intellectual disability	22102821	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	22522925	CNVD
Neurodevelopmental disorder	22521361	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:79418400-79451000	Weak transcription	Fetal Stomach	stomach
2	chr9:79435600-79455800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr9:79441400-79461000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr9:79449000-79452400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr9:79449000-79452600	Enhancers	Rectal Smooth Muscle	rectum
6	chr9:79449200-79451600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr9:79449200-79451600	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr9:79449400-79451600	Enhancers	Brain Hippocampus Middle	brain
9	chr9:79449400-79451600	Enhancers	Brain Substantia Nigra	brain
10	chr9:79449400-79451800	Enhancers	NH-A	brain
11	chr9:79449600-79451200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr9:79449600-79451200	Enhancers	Adipose Nuclei	Adipose
13	chr9:79449600-79451600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr9:79449600-79451600	Enhancers	HSMMtube	muscle
15	chr9:79449600-79451800	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr9:79449800-79451200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:79449800-79451200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr9:79449800-79451200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr9:79449800-79451200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr9:79449800-79451200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr9:79449800-79451400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr9:79449800-79451400	Active TSS	Stomach Smooth Muscle	stomach
23	chr9:79449800-79451600	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr9:79449800-79451600	Enhancers	A549	lung
25	chr9:79450000-79451000	Weak transcription	Aorta	Aorta
26	chr9:79450000-79451000	Weak transcription	Colon Smooth Muscle	Colon
27	chr9:79450000-79451000	Active TSS	Skeletal Muscle Female	skeletal muscle
28	chr9:79450000-79451600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr9:79450000-79454200	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr9:79450000-79478400	Weak transcription	Brain Angular Gyrus	brain
31	chr9:79450200-79451000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr9:79450200-79451000	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr9:79450200-79451200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
34	chr9:79450400-79451000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr9:79450600-79451000	Enhancers	NHEK	skin
36	chr9:79450600-79451000	Enhancers	Osteobl	bone
37	chr9:79450600-79451200	Enhancers	Brain Cingulate Gyrus	brain
38	chr9:79450600-79451400	Enhancers	NHLF	lung
39	chr9:79450800-79451000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr9:79450800-79451000	Flanking Active TSS	HSMM	muscle
41	chr9:79450800-79451200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:79450800-79451200	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr9:79450800-79451200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr9:79450800-79451200	Enhancers	Esophagus	oesophagus
45	chr9:79450800-79451400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr9:79450800-79451400	Enhancers	Brain Anterior Caudate	brain
47	chr9:79450800-79451400	Enhancers	Ovary	ovary
48	chr9:79450800-79451400	Flanking Active TSS	NHDF-Ad	bronchial
49	chr9:79451000-79451200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr9:79451000-79451200	Enhancers	Aorta	Aorta

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