Variant report

Variant	nsv886307
Chromosome Location	chr6:80724666-80765111
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:128)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:128 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr6:80739154-80739511	GM12878	blood:	n/a	n/a
2	BCLAF1	chr6:80739065-80739571	GM12878	blood:	n/a	n/a
3	CEBPB	chr6:80748846-80749099	K562	blood:	n/a	chr6:80749021-80749032 chr6:80749019-80749032
4	CEBPB	chr6:80732540-80732829	IMR90	lung:	n/a	n/a
5	CTCF	chr6:80754440-80754590	HEEpiC	esophagus:	n/a	n/a
6	CTCF	chr6:80756600-80756750	HPF	lung:	n/a	n/a
7	CTCF	chr6:80762160-80762276	Kidney_OC	kidney:	n/a	n/a
8	CTCF	chr6:80756756-80756842	ProgFib	skin:	n/a	n/a
9	CTCF	chr6:80758416-80758445	GM13976	blood:	n/a	n/a
10	CUX1	chr6:80745040-80745074	K562	blood:	n/a	n/a
11	E2F4	chr6:80741785-80741959	MCF10A-Er-Src	breast:	n/a	n/a
12	E2F4	chr6:80754785-80754787	MCF10A-Er-Src	breast:	n/a	n/a
13	EP300	chr6:80731355-80731565	SK-N-SH_RA	brain:	n/a	n/a
14	EP300	chr6:80729511-80729680	K562	blood:	n/a	n/a
15	FOS	chr6:80732565-80732909	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr6:80732428-80732916	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr6:80732585-80732889	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr6:80732575-80732929	MCF10A-Er-Src	breast:	n/a	n/a
19	FOXA2	chr6:80730182-80730455	HepG2	liver:	n/a	n/a
20	FOXA2	chr6:80763454-80764075	A549	lung:	n/a	n/a
21	GATA3	chr6:80733495-80734021	MCF-7	breast:	n/a	chr6:80733606-80733622
22	GATA3	chr6:80733287-80733991	SK-N-SH	brain:	n/a	chr6:80733606-80733622
23	GATA3	chr6:80725842-80726413	SK-N-SH	brain:	n/a	n/a
24	GATA3	chr6:80733429-80733936	MCF-7	breast:	n/a	chr6:80733606-80733622
25	GATA3	chr6:80726440-80727066	SK-N-SH	brain:	n/a	n/a
26	GATA3	chr6:80743625-80743847	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr6:80733297-80733993	SK-N-SH	brain:	n/a	chr6:80733606-80733622
28	GATA3	chr6:80733671-80733882	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr6:80732352-80733059	SK-N-SH	brain:	n/a	n/a
30	JUN	chr6:80732530-80732914	HUVEC	blood vessel:	n/a	n/a
31	JUN	chr6:80750626-80750681	K562	blood:	n/a	n/a
32	JUN	chr6:80733547-80733680	K562	blood:	n/a	chr6:80733647-80733655 chr6:80733648-80733655
33	JUND	chr6:80732222-80732947	SK-N-SH	brain:	n/a	n/a
34	JUND	chr6:80732386-80732957	SK-N-SH	brain:	n/a	n/a
35	MAFF	chr6:80738324-80738691	K562	blood:	n/a	chr6:80738494-80738512
36	MAFF	chr6:80732609-80732875	HepG2	liver:	n/a	chr6:80732730-80732748
37	MAFF	chr6:80738328-80738705	HepG2	liver:	n/a	chr6:80738494-80738512
38	MAFF	chr6:80732703-80732866	K562	blood:	n/a	chr6:80732730-80732748
39	MAFK	chr6:80732537-80732908	IMR90	lung:	n/a	chr6:80732731-80732746
40	MAFK	chr6:80738321-80738695	HepG2	liver:	n/a	chr6:80738496-80738511
41	MAFK	chr6:80732735-80732785	HepG2	liver:	n/a	n/a
42	MAFK	chr6:80738326-80738688	HepG2	liver:	n/a	chr6:80738496-80738511
43	MAFK	chr6:80738263-80738742	GM12878	blood:	n/a	chr6:80738496-80738511
44	MAFK	chr6:80738327-80738684	H1-hESC	embryonic stem cell:	n/a	chr6:80738496-80738511
45	MAFK	chr6:80732646-80732902	HepG2	liver:	n/a	chr6:80732731-80732746
46	MAFK	chr6:80738327-80738686	K562	blood:	n/a	chr6:80738496-80738511
47	MAFK	chr6:80738320-80738700	IMR90	lung:	n/a	chr6:80738496-80738511
48	MAFK	chr6:80738327-80738682	Hela-S3	cervix:	n/a	chr6:80738496-80738511
49	MAZ	chr6:80730116-80730259	HepG2	liver:	n/a	n/a
50	MEF2A	chr6:80732384-80733051	SK-N-SH	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:80731107-80731157	SAEC	small airway:	n/a
2	chr6:80731107-80731157	ProgFib	skin:	n/a
3	chr6:80731107-80731157	RPTEC	kidney:	n/a
4	chr6:80731107-80731157	NHDF-neo	bronchial:	n/a
5	chr6:80731107-80731157	HMEC	breast:	n/a
6	chr6:80731107-80731157	GM12892	blood:	n/a
7	chr6:80731107-80731157	HIPEpiC	eye:	n/a
8	chr6:80731107-80731157	MCF10A-Er-Src	breast:	n/a
9	chr6:80731107-80731157	H1-hESC	embryonic stem cell:	embryo
10	chr6:80731107-80731157	Hepatocyte	liver:	n/a
11	chr6:80731107-80731157	SK-N-SH	brain:	n/a
12	chr6:80731107-80731157	Caco-2	colon:	n/a
13	chr6:80731107-80731157	AG04449	skin:	fetal
14	chr6:80731107-80731157	HAEpiC	amniotic membrane:	n/a
15	chr6:80731107-80731157	GM12891	blood:	n/a
16	chr6:80731107-80731157	HUVEC	blood vessel:	n/a
17	chr6:80731107-80731157	Jurkat	blood:	n/a
18	chr6:80731107-80731157	GM06990	blood:	n/a
19	chr6:80731107-80731157	CMK	blood:	n/a
20	chr6:80731107-80731157	AoSMC	blood vessel:	n/a
21	chr6:80731107-80731157	GM12878	blood:	n/a
22	chr6:80731107-80731157	SK-N-MC	brain:	n/a
23	chr6:80731107-80731157	HEEpiC	esophagus:	n/a
24	chr6:80731107-80731157	PFSK-1	brain:	n/a
25	chr6:80731107-80731157	HCM	heart:	n/a
26	chr6:80731107-80731157	NT2-D1	testis:	n/a
27	chr6:80731107-80731157	BE2_C	brain:	n/a
28	chr6:80731107-80731157	SK-N-SH_RA	brain:	n/a
29	chr6:80731107-80731157	PANC-1	pancreas:	n/a
30	chr6:80731107-80731157	HRCEpiC	kidney:	n/a
31	chr6:80731107-80731157	ovcar-3	ovarian:	n/a
32	chr6:80731107-80731157	LNCaP	prostate:	n/a
33	chr6:80731107-80731157	AG10803	skin:	n/a
34	chr6:80731107-80731157	HRE	kidney:	n/a
35	chr6:80731107-80731157	NB4	blood:	n/a
36	chr6:80731107-80731157	SKMC	muscle:	n/a
37	chr6:80731107-80731157	NHBE	bronchial:	n/a
38	chr6:80731107-80731157	ECC-1	luminal epithelium:	n/a
39	chr6:80731107-80731157	MCF-7	breast:	n/a
40	chr6:80731107-80731157	IMR90	lung:	fetal
41	chr6:80731107-80731157	NH-A	brain:	n/a
42	chr6:80731107-80731157	HCT-116	colon:	n/a
43	chr6:80731107-80731157	AG04450	lung:	fetal
44	chr6:80731107-80731157	HepG2	liver:	n/a
45	chr6:80731107-80731157	A549	lung:	n/a
46	chr6:80731107-80731157	U87	brain:	n/a
47	chr6:80731107-80731157	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:80731107-80731157	HCF	heart:	n/a
49	chr6:80731107-80731157	GM19239	blood:	n/a
50	chr6:80731107-80731157	HCPEpiC	choroid plexus:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:80713136..80715748-chr6:80737826..80739442,2	K562	blood:
2	chr6:80744876..80746467-chr6:80815463..80817793,2	K562	blood:
3	chr6:80725148..80727689-chr6:80727866..80729792,3	K562	blood:
4	chr6:80729038..80731808-chr6:80734179..80735842,2	K562	blood:
5	chr6:80731473..80734540-chr6:80736888..80739701,3	K562	blood:
6	chr6:80742236..80743849-chr6:80785962..80787542,2	K562	blood:
7	chr6:80730895..80732973-chr6:80736170..80739701,4	K562	blood:
8	chr6:80743018..80745261-chr6:80747268..80749028,2	MCF-7	breast:
9	chr6:80733040..80735460-chr6:80736846..80739439,3	K562	blood:
10	chr6:80717310..80719454-chr6:80764068..80766246,2	K562	blood:
11	chr6:80733040..80735460-chr6:80736846..80739439,3	K562	blood:
12	chr6:80717535..80719093-chr6:80734932..80736458,2	K562	blood:
13	chr6:80720575..80723438-chr6:80727124..80728822,2	MCF-7	breast:
14	chr6:80731473..80734540-chr6:80736888..80739701,3	K562	blood:
15	chr6:80729038..80731808-chr6:80734179..80735842,2	K562	blood:
16	chr6:80724231..80726532-chr6:80730064..80732881,2	K562	blood:
17	chr6:80725148..80727689-chr6:80727866..80729792,3	K562	blood:
18	chr6:80725547..80727630-chr6:80735210..80737325,2	K562	blood:
19	chr6:80722394..80725312-chr6:80736793..80739743,2	MCF-7	breast:
20	chr6:80717752..80719460-chr6:80749306..80750878,2	K562	blood:
21	chr6:80730895..80732973-chr6:80736170..80739701,4	K562	blood:
22	chr6:80719003..80721359-chr6:80737643..80739358,2	K562	blood:
23	chr6:80715006..80717903-chr6:80744998..80747221,3	K562	blood:
24	chr6:80712691..80715749-chr6:80750056..80753128,3	K562	blood:
25	chr6:80725547..80727630-chr6:80735210..80737325,2	K562	blood:
26	chr6:80724231..80726532-chr6:80730064..80732881,2	K562	blood:
27	chr6:80726819..80729149-chr6:80732452..80734018,2	K562	blood:
28	chr6:80726819..80729149-chr6:80732452..80734018,2	K562	blood:
29	chr6:80745121..80747021-chr6:80747136..80749141,2	MCF-7	breast:

No data

Variant related genes	Relation type
TTK	TF binding region
TTK	CpG island
ENSG00000083123	chromatin interactions
ENSG00000112742	chromatin interactions

Extended variants
information (count: 1661 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1661 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12528948	chr6:80724666-80724667	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548404084	chr6:80724681-80724682	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146595473	chr6:80724693-80724694	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533594083	chr6:80724700-80724701	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148775460	chr6:80724745-80724746	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538527909	chr6:80724748-80724749	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs72902781	chr6:80724751-80724752	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs142443463	chr6:80724755-80724756	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568717302	chr6:80724785-80724786	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556578127	chr6:80724794-80724795	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs55956173	chr6:80724858-80724859	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs10673679	chr6:80724906-80724907	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368874813	chr6:80724907-80724908	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs397734149	chr6:80724909-80724910	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542169917	chr6:80724973-80724974	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79996900	chr6:80725000-80725001	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35213475	chr6:80725007-80725008	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs541502267	chr6:80725010-80725011	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs239569	chr6:80725052-80725053	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs151333944	chr6:80725117-80725118	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550244743	chr6:80725182-80725183	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62405969	chr6:80725254-80725255	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs377070248	chr6:80725279-80725280	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140438689	chr6:80725291-80725292	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538008785	chr6:80725299-80725300	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568216122	chr6:80725309-80725310	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563712065	chr6:80725316-80725317	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547071471	chr6:80725353-80725354	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570261511	chr6:80725386-80725387	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539039988	chr6:80725482-80725483	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73476022	chr6:80725497-80725498	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187323371	chr6:80725516-80725517	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191830185	chr6:80725521-80725522	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs151654	chr6:80725609-80725610	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs150413836	chr6:80725611-80725612	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541674099	chr6:80725622-80725623	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs62405970	chr6:80725737-80725738	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs564568119	chr6:80725765-80725766	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372368072	chr6:80725788-80725789	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147692801	chr6:80725800-80725801	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183612377	chr6:80725805-80725806	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561409011	chr6:80725810-80725811	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563651462	chr6:80725862-80725863	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186870241	chr6:80725926-80725927	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs34968483	chr6:80725976-80725977	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs151655	chr6:80725993-80725994	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs527484073	chr6:80725994-80725995	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190125742	chr6:80726032-80726033	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570323739	chr6:80726070-80726071	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532816327	chr6:80726106-80726107	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:80714800-80738800	Weak transcription	Small Intestine	intestine
2	chr6:80715000-80730400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:80715000-80748000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr6:80715000-80752200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr6:80715000-80752400	Weak transcription	Placenta	Placenta
6	chr6:80715200-80726000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr6:80715200-80727000	Weak transcription	Fetal Muscle Trunk	muscle
8	chr6:80715200-80730800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:80715200-80734000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr6:80715200-80734400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:80715200-80739200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr6:80715200-80749600	Weak transcription	Fetal Intestine Small	intestine
13	chr6:80715200-80752000	Weak transcription	Primary B cells from cord blood	blood
14	chr6:80715200-80752200	Weak transcription	Primary T cells from cord blood	blood
15	chr6:80715400-80726000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr6:80715400-80727000	Weak transcription	Fetal Muscle Leg	muscle
17	chr6:80715400-80729400	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr6:80715400-80742200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr6:80715400-80743200	Weak transcription	Brain Germinal Matrix	brain
20	chr6:80715400-80745400	Weak transcription	Fetal Lung	lung
21	chr6:80715400-80755000	Weak transcription	Duodenum Mucosa	Duodenum
22	chr6:80715400-80756800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:80715600-80725200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr6:80715600-80739200	Weak transcription	Fetal Stomach	stomach
25	chr6:80715600-80754400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr6:80715600-80763800	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr6:80715800-80733400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:80715800-80753600	Strong transcription	HUES48 Cell Line	embryonic stem cell
29	chr6:80715800-80753800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
30	chr6:80715800-80754400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr6:80716000-80726000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr6:80716000-80728600	Strong transcription	HUES6 Cell Line	embryonic stem cell
33	chr6:80716000-80729400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:80716000-80739200	Weak transcription	NHEK	skin
35	chr6:80716000-80743600	Weak transcription	Fetal Heart	heart
36	chr6:80716200-80725200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr6:80716200-80727800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:80716200-80728000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr6:80716200-80754600	Strong transcription	HUES64 Cell Line	embryonic stem cell
40	chr6:80716400-80727800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr6:80716800-80753600	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr6:80717000-80728000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr6:80717400-80724800	Strong transcription	NH-A	brain
44	chr6:80717400-80727400	Strong transcription	HUVEC	blood vessel
45	chr6:80717400-80728000	Strong transcription	H1 Cell Line	embryonic stem cell
46	chr6:80717400-80739200	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr6:80717600-80726800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr6:80717600-80727800	Strong transcription	HSMM	muscle
49	chr6:80718000-80728000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr6:80718000-80728000	Strong transcription	Fetal Thymus	thymus

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