Variant report

Variant	nsv886665
Chromosome Location	chr6:131518894-131611309
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	ATF2	chr6:131520738-131521260	GM12878	blood:	n/a	n/a
2	ATF2	chr6:131602635-131603046	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr6:131520913-131521168	GM12878	blood:	n/a	n/a
4	BCLAF1	chr6:131520780-131521237	GM12878	blood:	n/a	n/a
5	BHLHE40	chr6:131520903-131521363	GM12878	blood:	n/a	n/a
6	BRCA1	chr6:131600918-131600951	GM12878	blood:	n/a	n/a
7	BRCA1	chr6:131520861-131521007	GM12878	blood:	n/a	n/a
8	CEBPB	chr6:131552295-131552592	IMR90	lung:	n/a	n/a
9	CEBPB	chr6:131582109-131582484	IMR90	lung:	n/a	chr6:131582286-131582297
10	CEBPB	chr6:131582113-131582490	K562	blood:	n/a	chr6:131582286-131582297
11	CEBPB	chr6:131582217-131582460	ECC-1	luminal epithelium:	n/a	chr6:131582286-131582297
12	CEBPB	chr6:131534127-131534395	A549	lung:	n/a	chr6:131534279-131534290 chr6:131534277-131534294
13	CEBPB	chr6:131576868-131577048	HepG2	liver:	n/a	chr6:131576977-131576988
14	CEBPB	chr6:131520797-131521134	HepG2	liver:	n/a	n/a
15	CEBPB	chr6:131582186-131582336	HepG2	liver:	n/a	chr6:131582286-131582297
16	CEBPB	chr6:131577143-131577459	MCF-7	breast:	n/a	n/a
17	CEBPB	chr6:131520882-131521121	K562	blood:	n/a	n/a
18	CEBPB	chr6:131582226-131582427	ECC-1	luminal epithelium:	n/a	chr6:131582286-131582297
19	CEBPB	chr6:131552287-131552605	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr6:131534181-131534381	K562	blood:	n/a	chr6:131534279-131534290 chr6:131534277-131534294
21	CEBPB	chr6:131520756-131521212	MCF-7	breast:	n/a	n/a
22	CEBPB	chr6:131520790-131521154	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr6:131582217-131582400	MCF-7	breast:	n/a	chr6:131582286-131582297
24	CEBPB	chr6:131577172-131577461	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr6:131582125-131582475	H1-hESC	embryonic stem cell:	n/a	chr6:131582286-131582297
26	CEBPB	chr6:131577153-131577476	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr6:131552291-131552582	A549	lung:	n/a	n/a
28	CEBPB	chr6:131582116-131582482	HepG2	liver:	n/a	chr6:131582286-131582297
29	CEBPB	chr6:131582120-131582439	A549	lung:	n/a	chr6:131582286-131582297
30	CEBPB	chr6:131582205-131582493	A549	lung:	n/a	chr6:131582286-131582297
31	CEBPB	chr6:131576952-131576993	A549	lung:	n/a	chr6:131576977-131576988
32	CEBPB	chr6:131576884-131577411	H1-hESC	embryonic stem cell:	n/a	chr6:131576977-131576988
33	CEBPB	chr6:131520841-131521141	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr6:131582178-131582378	Hela-S3	cervix:	n/a	chr6:131582286-131582297
35	CEBPB	chr6:131534133-131534453	HepG2	liver:	n/a	chr6:131534279-131534290 chr6:131534277-131534294
36	CEBPB	chr6:131533164-131533549	IMR90	lung:	n/a	chr6:131533354-131533365
37	CEBPB	chr6:131602822-131603171	IMR90	lung:	n/a	chr6:131602966-131602977 chr6:131602983-131602994
38	CEBPB	chr6:131582217-131582449	A549	lung:	n/a	chr6:131582286-131582297
39	CEBPB	chr6:131534108-131534455	IMR90	lung:	n/a	chr6:131534279-131534290 chr6:131534277-131534294
40	CEBPB	chr6:131602692-131603125	H1-hESC	embryonic stem cell:	n/a	chr6:131602966-131602977 chr6:131602983-131602994
41	CEBPB	chr6:131602824-131603155	HepG2	liver:	n/a	chr6:131602966-131602977 chr6:131602983-131602994
42	CEBPB	chr6:131537995-131537998	HepG2	liver:	n/a	n/a
43	CEBPB	chr6:131576865-131577396	IMR90	lung:	n/a	chr6:131576977-131576988
44	CHD1	chr6:131520939-131521123	GM12878	blood:	n/a	n/a
45	CHD2	chr6:131520751-131521277	GM12878	blood:	n/a	n/a
46	CREB1	chr6:131602410-131603057	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr6:131520940-131521090	HCM	heart:	n/a	chr6:131520992-131521013 chr6:131521064-131521082
48	CTCF	chr6:131520818-131521134	GM12891	blood:	n/a	chr6:131520992-131521013 chr6:131521064-131521082
49	CTCF	chr6:131520871-131521109	MCF-7	breast:	n/a	chr6:131520992-131521013 chr6:131521064-131521082
50	CTCF	chr6:131520940-131521090	HCPEpiC	choroid plexus:	n/a	chr6:131520992-131521013 chr6:131521064-131521082

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:131571669-131571719	AoSMC	blood vessel:	n/a
2	chr6:131602870-131602920	PANC-1	pancreas:	n/a
3	chr6:131571669-131571719	AoSMC	blood vessel:	n/a
4	chr6:131602870-131602920	PANC-1	pancreas:	n/a
5	chr6:131571435-131571485	Caco-2	colon:	n/a
6	chr6:131548063-131548113	AG09309	skin:	n/a
7	chr6:131548063-131548113	AG10803	skin:	n/a
8	chr6:131520996-131521046	T-47D	breast:	n/a
9	chr6:131571435-131571485	GM12891	blood:	n/a
10	chr6:131571669-131571719	BE2_C	brain:	n/a
11	chr6:131520996-131521046	HMEC	breast:	n/a
12	chr6:131520996-131521046	U87	brain:	n/a
13	chr6:131548063-131548113	MCF10A-Er-Src	breast:	n/a
14	chr6:131571435-131571485	HepG2	liver:	n/a
15	chr6:131571669-131571719	AG09309	skin:	n/a
16	chr6:131602870-131602920	ProgFib	skin:	n/a
17	chr6:131571669-131571719	Jurkat	blood:	n/a
18	chr6:131520996-131521046	Caco-2	colon:	n/a
19	chr6:131602870-131602920	HRCEpiC	kidney:	n/a
20	chr6:131571435-131571485	SKMC	muscle:	n/a
21	chr6:131602870-131602920	NHDF-neo	bronchial:	n/a
22	chr6:131520996-131521046	Hela-S3	cervix:	n/a
23	chr6:131571435-131571485	NHBE	bronchial:	n/a
24	chr6:131571669-131571719	GM19239	blood:	n/a
25	chr6:131602870-131602920	AG09319	gingival:	n/a
26	chr6:131548063-131548113	HMEC	breast:	n/a
27	chr6:131571669-131571719	RPTEC	kidney:	n/a
28	chr6:131571435-131571485	AG04450	lung:	fetal
29	chr6:131602870-131602920	HCT-116	colon:	n/a
30	chr6:131571669-131571719	NH-A	brain:	n/a
31	chr6:131571435-131571485	BJ	skin:	n/a
32	chr6:131520996-131521046	PFSK-1	brain:	n/a
33	chr6:131571669-131571719	NHDF-neo	bronchial:	n/a
34	chr6:131602870-131602920	T-47D	breast:	n/a
35	chr6:131571669-131571719	SAEC	small airway:	n/a
36	chr6:131548063-131548113	HPAEpiC	pulmonary alveolar:	n/a
37	chr6:131520996-131521046	PANC-1	pancreas:	n/a
38	chr6:131571435-131571485	GM12892	blood:	n/a
39	chr6:131602870-131602920	AG09309	skin:	n/a
40	chr6:131571669-131571719	HCF	heart:	n/a
41	chr6:131602870-131602920	SK-N-SH_RA	brain:	n/a
42	chr6:131571669-131571719	PFSK-1	brain:	n/a
43	chr6:131571435-131571485	HRPEpiC	eye:	n/a
44	chr6:131548063-131548113	RPTEC	kidney:	n/a
45	chr6:131571669-131571719	HEK293	kidney:	embryo
46	chr6:131548063-131548113	LNCaP	prostate:	n/a
47	chr6:131571435-131571485	Hela-S3	cervix:	n/a
48	chr6:131520996-131521046	HRPEpiC	eye:	n/a
49	chr6:131520996-131521046	HL-60	blood:	n/a
50	chr6:131571435-131571485	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:131526816..131527805-chr6:131855115..131855774,2	MCF-7	breast:
2	chr6:131562493..131564861-chr6:131566716..131568915,2	MCF-7	breast:
3	chr6:131520473..131521448-chr6:131582980..131583832,4	MCF-7	breast:
4	chr6:131591823..131594173-chr6:131613820..131615536,2	K562	blood:
5	chr6:131526933..131527448-chr6:131918295..131918857,2	MCF-7	breast:
6	chr6:131574679..131577194-chr6:131577773..131580608,2	MCF-7	breast:
7	chr6:131562493..131564861-chr6:131566716..131568915,2	MCF-7	breast:
8	chr6:131574679..131577194-chr6:131577773..131580608,2	MCF-7	breast:

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	AKAP7	hsa-miR-375	chr6:131604029-131604050
2	AKAP7	hsa-miR-375	chr6:131604183-131604206

Variant related genes	Relation type
AKAP7	TF binding region
AKAP7	CpG island
ENSG00000118507	chromatin interactions

Extended variants
information (count: 3248 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3248 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3850238	chr6:131518894-131518895	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576525709	chr6:131518920-131518921	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs546953124	chr6:131518921-131518922	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs568439837	chr6:131518939-131518940	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs544126599	chr6:131518941-131518942	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs556071677	chr6:131518952-131518953	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs535867382	chr6:131518953-131518954	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs185642861	chr6:131519000-131519001	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs375640910	chr6:131519057-131519058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190231929	chr6:131519116-131519117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541426422	chr6:131519117-131519118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559744841	chr6:131519167-131519168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs75117348	chr6:131519230-131519231	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs62422459	chr6:131519236-131519237	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs144101069	chr6:131519339-131519340	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs530605546	chr6:131519369-131519370	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs566022595	chr6:131519385-131519386	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs574839238	chr6:131519632-131519633	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs77754500	chr6:131519663-131519664	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs150996989	chr6:131519695-131519696	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs569419045	chr6:131519696-131519697	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs80042486	chr6:131519700-131519701	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs571126163	chr6:131519711-131519712	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs115972620	chr6:131519728-131519729	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs180859999	chr6:131519732-131519733	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs550388012	chr6:131519747-131519748	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs114698986	chr6:131519798-131519799	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs75701714	chr6:131519806-131519807	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs556135092	chr6:131519882-131519883	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs574398019	chr6:131519887-131519888	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs184979478	chr6:131519907-131519908	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs188617967	chr6:131519916-131519917	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs577925431	chr6:131519923-131519924	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs374183019	chr6:131519928-131519929	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs181141210	chr6:131519940-131519941	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs557700517	chr6:131519962-131519963	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs140907752	chr6:131519991-131519992	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs149980823	chr6:131520008-131520009	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs139541278	chr6:131520036-131520037	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs560701698	chr6:131520078-131520079	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs528389829	chr6:131520090-131520091	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs546453439	chr6:131520099-131520100	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs35229166	chr6:131520115-131520116	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs566128485	chr6:131520120-131520121	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs1190791	chr6:131520124-131520125	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs550696639	chr6:131520127-131520128	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs568849174	chr6:131520177-131520178	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs75809603	chr6:131520178-131520179	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs549602955	chr6:131520199-131520200	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs540127193	chr6:131520258-131520259	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1744 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131457600-131520800	Weak transcription	Right Ventricle	heart
2	chr6:131488200-131534800	Weak transcription	Gastric	stomach
3	chr6:131505000-131521000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:131505000-131521800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:131505200-131522600	Weak transcription	HSMMtube	muscle
6	chr6:131505800-131534600	Weak transcription	Brain Substantia Nigra	brain
7	chr6:131505800-131534800	Weak transcription	Pancreas	Pancrea
8	chr6:131506400-131520800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr6:131506600-131520600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr6:131506600-131520600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr6:131506600-131520600	Weak transcription	Spleen	Spleen
12	chr6:131506600-131520800	Weak transcription	Lung	lung
13	chr6:131506600-131523800	Weak transcription	HepG2	liver
14	chr6:131506600-131524000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:131506600-131529800	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr6:131506600-131532000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr6:131506800-131551800	Weak transcription	Ovary	ovary
18	chr6:131507000-131520400	Weak transcription	Liver	Liver
19	chr6:131510400-131534800	Weak transcription	Small Intestine	intestine
20	chr6:131513000-131520800	Weak transcription	Aorta	Aorta
21	chr6:131513000-131520800	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr6:131513000-131522600	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr6:131513000-131523000	Weak transcription	Placenta	Placenta
24	chr6:131513200-131520600	Weak transcription	Left Ventricle	heart
25	chr6:131513200-131526400	Weak transcription	Fetal Intestine Small	intestine
26	chr6:131513200-131536400	Weak transcription	Esophagus	oesophagus
27	chr6:131513400-131520600	Weak transcription	Fetal Stomach	stomach
28	chr6:131513800-131520200	Weak transcription	Adipose Nuclei	Adipose
29	chr6:131514400-131519800	Weak transcription	Stomach Smooth Muscle	stomach
30	chr6:131514400-131529800	Weak transcription	Brain Germinal Matrix	brain
31	chr6:131514400-131541400	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr6:131514600-131520600	Weak transcription	Fetal Lung	lung
33	chr6:131514600-131521200	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr6:131514800-131520600	Weak transcription	Brain Hippocampus Middle	brain
35	chr6:131516000-131519200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr6:131516400-131520600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr6:131516600-131521200	Weak transcription	Rectal Smooth Muscle	rectum
38	chr6:131517000-131520800	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr6:131517800-131519600	Enhancers	Dnd41	blood
40	chr6:131518000-131520000	Weak transcription	Brain Anterior Caudate	brain
41	chr6:131518200-131519200	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr6:131518200-131519800	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr6:131518200-131520800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr6:131518200-131520800	Enhancers	Primary T cells from cord blood	blood
45	chr6:131518200-131520800	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr6:131518200-131520800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr6:131518200-131521000	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr6:131518200-131521000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr6:131518200-131521200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr6:131518200-131525600	Weak transcription	Fetal Brain Male	brain

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