Variant report

Variant	nsv591363
Chromosome Location	chr3:119316828-119345950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:516)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:119342802-119343437	GM12878	blood:	n/a	n/a
2	ATF2	chr3:119315942-119318112	GM12878	blood:	n/a	n/a
3	ATF2	chr3:119342686-119343340	GM12878	blood:	n/a	n/a
4	ATF2	chr3:119319437-119320241	GM12878	blood:	n/a	n/a
5	ATF2	chr3:119316171-119318970	GM12878	blood:	n/a	n/a
6	ATF2	chr3:119318262-119320560	GM12878	blood:	n/a	n/a
7	BACH1	chr3:119319593-119319815	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr3:119316751-119317180	GM12878	blood:	n/a	n/a
9	BATF	chr3:119332101-119332332	GM12878	blood:	n/a	n/a
10	BATF	chr3:119317199-119317631	GM12878	blood:	n/a	n/a
11	BATF	chr3:119319513-119319956	GM12878	blood:	n/a	n/a
12	BATF	chr3:119316856-119317125	GM12878	blood:	n/a	n/a
13	BATF	chr3:119323776-119323995	GM12878	blood:	n/a	chr3:119323902-119323913 chr3:119323903-119323913
14	BCL11A	chr3:119316773-119317613	GM12878	blood:	n/a	n/a
15	BCL3	chr3:119316624-119317763	GM12878	blood:	n/a	n/a
16	BCL3	chr3:119318231-119318854	GM12878	blood:	n/a	chr3:119318543-119318552
17	BCL3	chr3:119342739-119343363	GM12878	blood:	n/a	n/a
18	BCLAF1	chr3:119317146-119317826	GM12878	blood:	n/a	n/a
19	BCLAF1	chr3:119319438-119320103	GM12878	blood:	n/a	n/a
20	BCLAF1	chr3:119319433-119320288	GM12878	blood:	n/a	n/a
21	BCLAF1	chr3:119315811-119317043	GM12878	blood:	n/a	n/a
22	BCLAF1	chr3:119342774-119343237	GM12878	blood:	n/a	n/a
23	BCLAF1	chr3:119316211-119318576	GM12878	blood:	n/a	chr3:119318543-119318552
24	BHLHE40	chr3:119319671-119319988	K562	blood:	n/a	n/a
25	BHLHE40	chr3:119318204-119318696	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:119316293-119317958	GM12878	blood:	n/a	n/a
27	BHLHE40	chr3:119323736-119323916	GM12878	blood:	n/a	n/a
28	BHLHE40	chr3:119319425-119320133	GM12878	blood:	n/a	n/a
29	BRCA1	chr3:119318556-119318687	GM12878	blood:	n/a	n/a
30	BRCA1	chr3:119316831-119316913	GM12878	blood:	n/a	n/a
31	BRCA1	chr3:119319291-119319957	GM12878	blood:	n/a	n/a
32	CCNT2	chr3:119344653-119344853	K562	blood:	n/a	n/a
33	CEBPB	chr3:119316601-119318949	GM12878	blood:	n/a	chr3:119317085-119317098
34	CEBPB	chr3:119325269-119325491	A549	lung:	n/a	chr3:119325382-119325393 chr3:119325382-119325395
35	CHD1	chr3:119316263-119320189	GM12878	blood:	n/a	n/a
36	CHD1	chr3:119321628-119322097	GM12878	blood:	n/a	n/a
37	CHD2	chr3:119316648-119319935	GM12878	blood:	n/a	n/a
38	CHD2	chr3:119320141-119320411	GM12878	blood:	n/a	n/a
39	CTCF	chr3:119319498-119320155	GM12878	blood:	n/a	chr3:119319873-119319886 chr3:119319765-119319786 chr3:119319763-119319781
40	CTCF	chr3:119319700-119319850	RPTEC	kidney:	n/a	chr3:119319765-119319786 chr3:119319763-119319781
41	CTCF	chr3:119319680-119319830	GM12872	blood:	n/a	chr3:119319765-119319786 chr3:119319763-119319781
42	CTCF	chr3:119337828-119338012	GM12878	blood:	n/a	chr3:119337921-119337930
43	CTCF	chr3:119319660-119319810	K562	blood:	n/a	chr3:119319765-119319786 chr3:119319763-119319781
44	CTCF	chr3:119319700-119319850	WERI-Rb-1	eye:	n/a	chr3:119319765-119319786 chr3:119319763-119319781
45	CTCF	chr3:119337800-119337950	GM12875	blood:	n/a	chr3:119337921-119337930
46	CTCF	chr3:119319618-119319914	H1-hESC	embryonic stem cell:	n/a	chr3:119319873-119319886 chr3:119319765-119319786 chr3:119319763-119319781
47	CTCF	chr3:119319700-119319850	HBMEC	blood vessel:	n/a	chr3:119319765-119319786 chr3:119319763-119319781
48	CTCF	chr3:119337838-119338020	GM19240	blood:	n/a	chr3:119337921-119337930
49	CTCF	chr3:119319638-119319904	ProgFib	skin:	n/a	chr3:119319873-119319886 chr3:119319765-119319786 chr3:119319763-119319781
50	CTCF	chr3:119319700-119319850	HRE	kidney:	n/a	chr3:119319765-119319786 chr3:119319763-119319781

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:119316820-119316870	NT2-D1	testis:	n/a
2	chr3:119345741-119345791	RPTEC	kidney:	n/a
3	chr3:119316820-119316870	LNCaP	prostate:	n/a
4	chr3:119345741-119345791	HCF	heart:	n/a
5	chr3:119316820-119316870	HCT-116	colon:	n/a
6	chr3:119316820-119316870	PrEC	prostate:	n/a
7	chr3:119316820-119316870	NHDF-neo	bronchial:	n/a
8	chr3:119316820-119316870	T-47D	breast:	n/a
9	chr3:119345741-119345791	HL-60	blood:	n/a
10	chr3:119316820-119316870	SAEC	small airway:	n/a
11	chr3:119345741-119345791	NH-A	brain:	n/a
12	chr3:119345741-119345791	SK-N-MC	brain:	n/a
13	chr3:119345741-119345791	HRPEpiC	eye:	n/a
14	chr3:119345741-119345791	Jurkat	blood:	n/a
15	chr3:119316820-119316870	HCF	heart:	n/a
16	chr3:119345741-119345791	Caco-2	colon:	n/a
17	chr3:119345741-119345791	SAEC	small airway:	n/a
18	chr3:119345741-119345791	NB4	blood:	n/a
19	chr3:119316820-119316870	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:119345741-119345791	ProgFib	skin:	n/a
21	chr3:119316820-119316870	A549	lung:	n/a
22	chr3:119345741-119345791	AG04450	lung:	fetal
23	chr3:119316820-119316870	AG04450	lung:	fetal
24	chr3:119345741-119345791	NT2-D1	testis:	n/a
25	chr3:119345741-119345791	MCF10A-Er-Src	breast:	n/a
26	chr3:119316820-119316870	MCF-7	breast:	n/a
27	chr3:119316820-119316870	RPTEC	kidney:	n/a
28	chr3:119345741-119345791	GM12891	blood:	n/a
29	chr3:119316820-119316870	HepG2	liver:	n/a
30	chr3:119345741-119345791	HepG2	liver:	n/a
31	chr3:119316820-119316870	Hepatocyte	liver:	n/a
32	chr3:119345741-119345791	ECC-1	luminal epithelium:	n/a
33	chr3:119345741-119345791	IMR90	lung:	fetal
34	chr3:119316820-119316870	GM12892	blood:	n/a
35	chr3:119345741-119345791	MCF-7	breast:	n/a
36	chr3:119316820-119316870	GM12891	blood:	n/a
37	chr3:119316820-119316870	HRPEpiC	eye:	n/a
38	chr3:119316820-119316870	HRE	kidney:	n/a
39	chr3:119345741-119345791	BJ	skin:	n/a
40	chr3:119316820-119316870	Hela-S3	cervix:	n/a
41	chr3:119316820-119316870	SKMC	muscle:	n/a
42	chr3:119345741-119345791	PrEC	prostate:	n/a
43	chr3:119316820-119316870	HMEC	breast:	n/a
44	chr3:119316820-119316870	SK-N-SH_RA	brain:	n/a
45	chr3:119316820-119316870	GM19239	blood:	n/a
46	chr3:119345741-119345791	HIPEpiC	eye:	n/a
47	chr3:119345741-119345791	CMK	blood:	n/a
48	chr3:119316820-119316870	ProgFib	skin:	n/a
49	chr3:119316820-119316870	HUVEC	blood vessel:	n/a
50	chr3:119345741-119345791	PFSK-1	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:119337629..119339642-chr3:119343042..119344832,3	K562	blood:
2	chr3:119328437..119330333-chr3:119390205..119392685,2	K562	blood:
3	chr3:119337629..119339642-chr3:119343042..119344832,3	K562	blood:
4	chr3:119324918..119326771-chr3:119333086..119335282,2	K562	blood:
5	chr3:119324918..119326771-chr3:119333086..119335282,2	K562	blood:
6	chr3:119319313..119321262-chr3:119322045..119324226,2	MCF-7	breast:
7	chr3:119326064..119328703-chr3:119343379..119345422,2	MCF-7	breast:
8	chr3:119297101..119299038-chr3:119322847..119325406,2	MCF-7	breast:
9	chr3:119318615..119321815-chr3:119324739..119327300,3	K562	blood:
10	chr3:119214370..119217266-chr3:119338238..119340202,2	MCF-7	breast:
11	chr3:119344313..119346275-chr3:119356031..119358042,2	K562	blood:
12	chr3:119326194..119327898-chr3:119353631..119355784,2	K562	blood:
13	chr3:119297675..119300178-chr3:119317651..119319596,4	MCF-7	breast:
14	chr3:119319313..119321262-chr3:119322045..119324226,2	MCF-7	breast:
15	chr3:119321566..119324392-chr3:119394487..119396945,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADPRH-2	chr3:119317432-119317473	NONHSAT091396
2	lnc-ADPRH-2	chr3:119325621-119325944	NONHSAT091396

No data

Variant related genes	Relation type
PLA1A	TF binding region
PLA1A	CpG island
ENSG00000272967	chromatin interactions
ENSG00000242052	chromatin interactions
ENSG00000272662	chromatin interactions
ENSG00000144837	chromatin interactions
ENSG00000144843	chromatin interactions
ENSG00000138495	chromatin interactions

Extended variants
information (count: 1313 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1313 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1128293	chr3:119316828-119316829	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs182046280	chr3:119316851-119316852	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs186645237	chr3:119316861-119316862	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs62264534	chr3:119316881-119316882	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs369501392	chr3:119316882-119316883	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs373533804	chr3:119316884-119316885	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs139259153	chr3:119316952-119316953	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs141574051	chr3:119316972-119316973	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs543948270	chr3:119316973-119316974	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs368230946	chr3:119316978-119316979	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs562594370	chr3:119316979-119316980	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs558939339	chr3:119316991-119316992	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs529666653	chr3:119317009-119317010	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs143876428	chr3:119317058-119317059	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs566227461	chr3:119317081-119317082	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs561439650	chr3:119317106-119317107	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs75315923	chr3:119317130-119317131	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs75722870	chr3:119317131-119317132	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs74416330	chr3:119317132-119317133	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs147239376	chr3:119317163-119317164	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs547293768	chr3:119317169-119317170	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs544951859	chr3:119317181-119317182	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs553665453	chr3:119317240-119317241	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs2692623	chr3:119317279-119317280	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs34377856	chr3:119317311-119317312	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs190161555	chr3:119317342-119317343	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs139801572	chr3:119317379-119317380	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs569290255	chr3:119317386-119317387	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs536275829	chr3:119317404-119317405	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs554917407	chr3:119317437-119317438	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs9811104	chr3:119317459-119317460	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs182272680	chr3:119317517-119317518	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs145278108	chr3:119317541-119317542	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs574695017	chr3:119317561-119317562	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs376043175	chr3:119317576-119317577	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs368200684	chr3:119317607-119317608	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs372141511	chr3:119317631-119317632	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs186418529	chr3:119317696-119317697	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs562446864	chr3:119317702-119317703	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs574439984	chr3:119317712-119317713	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs190023201	chr3:119317729-119317730	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs11710365	chr3:119317751-119317752	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs147620590	chr3:119317769-119317770	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs555973924	chr3:119317787-119317788	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs75818941	chr3:119317807-119317808	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs565535862	chr3:119317824-119317825	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs532754127	chr3:119317888-119317889	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs111929342	chr3:119317930-119317931	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs79555895	chr3:119317950-119317951	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs569271276	chr3:119317961-119317962	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Glioblastoma multiforme	22286061	CNVD
Neurodevelopmental disorder	22521361	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:119299800-119318000	Weak transcription	Fetal Heart	heart
2	chr3:119310600-119319800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:119311000-119317600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr3:119314200-119317200	Enhancers	Lung	lung
5	chr3:119314400-119318600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:119314800-119317400	Enhancers	Primary B cells from peripheral blood	blood
7	chr3:119315000-119317800	Enhancers	Adipose Nuclei	Adipose
8	chr3:119315000-119318000	Enhancers	Psoas Muscle	Psoas
9	chr3:119315000-119320200	Enhancers	Left Ventricle	heart
10	chr3:119315200-119317000	Enhancers	A549	lung
11	chr3:119315200-119317000	Enhancers	HepG2	liver
12	chr3:119315200-119317000	Enhancers	HSMMtube	muscle
13	chr3:119315200-119317400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr3:119315400-119317600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:119315400-119319200	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr3:119315600-119317800	Weak transcription	Gastric	stomach
17	chr3:119315600-119319000	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr3:119315600-119319600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr3:119316000-119317200	Enhancers	HUVEC	blood vessel
20	chr3:119316000-119317400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr3:119316000-119319200	Weak transcription	Fetal Muscle Trunk	muscle
22	chr3:119316200-119317000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr3:119316200-119317000	Enhancers	Stomach Mucosa	stomach
24	chr3:119316200-119317200	Weak transcription	Right Atrium	heart
25	chr3:119316200-119318200	Enhancers	Fetal Kidney	kidney
26	chr3:119316200-119319400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr3:119316200-119319400	Weak transcription	Placenta	Placenta
28	chr3:119316200-119319600	Weak transcription	Spleen	Spleen
29	chr3:119316200-119340600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr3:119316400-119317400	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr3:119316400-119318200	Flanking Active TSS	Liver	Liver
32	chr3:119316400-119320600	Flanking Active TSS	GM12878-XiMat	blood
33	chr3:119316600-119317000	Enhancers	Osteobl	bone
34	chr3:119316600-119317800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr3:119316600-119320200	Enhancers	Right Ventricle	heart
36	chr3:119316800-119317000	Flanking Active TSS	Fetal Intestine Large	intestine
37	chr3:119316800-119317000	Flanking Active TSS	Fetal Intestine Small	intestine
38	chr3:119316800-119317000	Enhancers	Fetal Lung	lung
39	chr3:119316800-119317000	Enhancers	Ovary	ovary
40	chr3:119316800-119317000	Enhancers	Pancreas	Pancrea
41	chr3:119316800-119317000	Enhancers	Small Intestine	intestine
42	chr3:119316800-119317200	Weak transcription	Duodenum Mucosa	Duodenum
43	chr3:119316800-119317600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:119317000-119317400	Weak transcription	Ovary	ovary
45	chr3:119317000-119317400	Weak transcription	Pancreas	Pancrea
46	chr3:119317000-119317600	Enhancers	Fetal Intestine Small	intestine
47	chr3:119317000-119319000	Enhancers	Fetal Intestine Large	intestine
48	chr3:119317000-119319800	Weak transcription	Fetal Lung	lung
49	chr3:119317000-119319800	Weak transcription	HepG2	liver
50	chr3:119317000-119323800	Weak transcription	HSMMtube	muscle

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