Variant report

Variant	nsv886533
Chromosome Location	chr6:110067773-110126393
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	ARID3A	chr6:110114986-110115186	K562	blood:	n/a	n/a
2	ATF1	chr6:110093229-110093466	K562	blood:	n/a	n/a
3	ATF1	chr6:110125383-110125661	K562	blood:	n/a	n/a
4	ATF1	chr6:110114928-110115258	K562	blood:	n/a	n/a
5	ATF2	chr6:110090390-110090870	GM12878	blood:	n/a	n/a
6	ATF2	chr6:110117112-110117588	GM12878	blood:	n/a	n/a
7	ATF2	chr6:110090341-110090948	GM12878	blood:	n/a	n/a
8	BATF	chr6:110093219-110093492	GM12878	blood:	n/a	n/a
9	BATF	chr6:110090504-110090663	GM12878	blood:	n/a	n/a
10	BATF	chr6:110120842-110121143	GM12878	blood:	n/a	chr6:110121105-110121115
11	BCL11A	chr6:110090503-110090669	GM12878	blood:	n/a	n/a
12	BCL3	chr6:110117265-110117585	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:110123161-110123186	K562	blood:	n/a	n/a
14	BHLHE40	chr6:110117334-110117534	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:110094072-110094089	K562	blood:	n/a	n/a
16	BHLHE40	chr6:110112683-110112776	K562	blood:	n/a	n/a
17	BRCA1	chr6:110114897-110115456	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr6:110114820-110115406	HCT-116	colon:	n/a	n/a
19	CEBPB	chr6:110116345-110116468	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr6:110117183-110117751	GM12878	blood:	n/a	n/a
21	CEBPB	chr6:110118994-110119456	Hela-S3	cervix:	n/a	chr6:110119270-110119281 chr6:110119270-110119281
22	CEBPB	chr6:110093176-110093466	K562	blood:	n/a	n/a
23	CEBPB	chr6:110114309-110114649	HepG2	liver:	n/a	chr6:110114490-110114503
24	CEBPB	chr6:110093203-110093753	IMR90	lung:	n/a	n/a
25	CEBPB	chr6:110093199-110093496	K562	blood:	n/a	n/a
26	CEBPB	chr6:110114454-110115928	IMR90	lung:	n/a	chr6:110114490-110114503
27	CEBPB	chr6:110093139-110093553	K562	blood:	n/a	n/a
28	CEBPB	chr6:110097544-110097759	HepG2	liver:	n/a	chr6:110097669-110097680 chr6:110097671-110097680 chr6:110097670-110097681
29	CEBPB	chr6:110093233-110093457	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:110114340-110114560	A549	lung:	n/a	chr6:110114490-110114503
31	CEBPB	chr6:110114308-110115817	Hela-S3	cervix:	n/a	chr6:110114490-110114503
32	CEBPB	chr6:110093223-110093453	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr6:110116221-110116620	ECC-1	luminal epithelium:	n/a	n/a
34	CHD2	chr6:110114930-110115913	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr6:110117296-110117461	GM12878	blood:	n/a	n/a
36	CREB1	chr6:110114970-110115305	GM12878	blood:	n/a	n/a
37	CTCF	chr6:110104660-110104810	HEK293	kidney:	n/a	n/a
38	CTCF	chr6:110104600-110104750	HVMF	connective:	n/a	chr6:110104631-110104647 chr6:110104625-110104646 chr6:110104630-110104648
39	CTCF	chr6:110104523-110104753	HUVEC	blood vessel:	n/a	chr6:110104631-110104647 chr6:110104625-110104646 chr6:110104630-110104648
40	CTCF	chr6:110104513-110104694	SK-N-SH_RA	brain:	n/a	chr6:110104631-110104647 chr6:110104625-110104646 chr6:110104630-110104648
41	CTCF	chr6:110104540-110104690	HUVEC	blood vessel:	n/a	chr6:110104631-110104647 chr6:110104625-110104646 chr6:110104630-110104648
42	CTCF	chr6:110104560-110104710	AG09309	skin:	n/a	chr6:110104631-110104647 chr6:110104625-110104646 chr6:110104630-110104648
43	CTCF	chr6:110112580-110112730	HMF	breast:	n/a	n/a
44	CTCF	chr6:110112620-110112770	HRE	kidney:	n/a	n/a
45	CTCF	chr6:110104615-110104718	GM20000	blood:	n/a	chr6:110104631-110104647 chr6:110104625-110104646 chr6:110104630-110104648
46	CTCF	chr6:110104460-110104808	IMR90	lung:	n/a	chr6:110104631-110104647 chr6:110104625-110104646 chr6:110104630-110104648
47	CTCF	chr6:110104560-110104710	HRPEpiC	eye:	n/a	chr6:110104631-110104647 chr6:110104625-110104646 chr6:110104630-110104648
48	CTCF	chr6:110104460-110104610	HFF	foreskin:	n/a	n/a
49	CTCF	chr6:110104600-110104750	NB4	blood:	n/a	chr6:110104631-110104647 chr6:110104625-110104646 chr6:110104630-110104648
50	CTCF	chr6:110104440-110104590	GM12870	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:110094833-110094883	HepG2	liver:	n/a
2	chr6:110104633-110104683	LNCaP	prostate:	n/a
3	chr6:110094833-110094883	AG04450	lung:	fetal
4	chr6:110115053-110115103	T-47D	breast:	n/a
5	chr6:110104633-110104683	CMK	blood:	n/a
6	chr6:110115053-110115103	HepG2	liver:	n/a
7	chr6:110115053-110115103	HCPEpiC	choroid plexus:	n/a
8	chr6:110115053-110115103	ovcar-3	ovarian:	n/a
9	chr6:110104633-110104683	BE2_C	brain:	n/a
10	chr6:110115053-110115103	SK-N-SH_RA	brain:	n/a
11	chr6:110094833-110094883	HCF	heart:	n/a
12	chr6:110094833-110094883	GM12892	blood:	n/a
13	chr6:110104633-110104683	ECC-1	luminal epithelium:	n/a
14	chr6:110104633-110104683	SAEC	small airway:	n/a
15	chr6:110104633-110104683	AoSMC	blood vessel:	n/a
16	chr6:110094833-110094883	MCF10A-Er-Src	breast:	n/a
17	chr6:110094833-110094883	ovcar-3	ovarian:	n/a
18	chr6:110104633-110104683	HCT-116	colon:	n/a
19	chr6:110094833-110094883	GM12891	blood:	n/a
20	chr6:110094833-110094883	NHDF-neo	bronchial:	n/a
21	chr6:110094833-110094883	SK-N-SH_RA	brain:	n/a
22	chr6:110115053-110115103	BE2_C	brain:	n/a
23	chr6:110104633-110104683	ovcar-3	ovarian:	n/a
24	chr6:110094833-110094883	U87	brain:	n/a
25	chr6:110094833-110094883	HCT-116	colon:	n/a
26	chr6:110115053-110115103	AG04449	skin:	fetal
27	chr6:110115053-110115103	HMEC	breast:	n/a
28	chr6:110104633-110104683	K562	blood:	n/a
29	chr6:110115053-110115103	HEEpiC	esophagus:	n/a
30	chr6:110104633-110104683	HAEpiC	amniotic membrane:	n/a
31	chr6:110104633-110104683	Hela-S3	cervix:	n/a
32	chr6:110094833-110094883	MCF-7	breast:	n/a
33	chr6:110104633-110104683	HEEpiC	esophagus:	n/a
34	chr6:110115053-110115103	HAEpiC	amniotic membrane:	n/a
35	chr6:110115053-110115103	LNCaP	prostate:	n/a
36	chr6:110115053-110115103	CMK	blood:	n/a
37	chr6:110094833-110094883	LNCaP	prostate:	n/a
38	chr6:110104633-110104683	MCF10A-Er-Src	breast:	n/a
39	chr6:110094833-110094883	T-47D	breast:	n/a
40	chr6:110104633-110104683	NHDF-neo	bronchial:	n/a
41	chr6:110094833-110094883	PFSK-1	brain:	n/a
42	chr6:110104633-110104683	HRCEpiC	kidney:	n/a
43	chr6:110094833-110094883	GM12878	blood:	n/a
44	chr6:110094833-110094883	IMR90	lung:	fetal
45	chr6:110115053-110115103	MCF10A-Er-Src	breast:	n/a
46	chr6:110094833-110094883	HCM	heart:	n/a
47	chr6:110094833-110094883	AG09319	gingival:	n/a
48	chr6:110104633-110104683	Caco-2	colon:	n/a
49	chr6:110115053-110115103	HCF	heart:	n/a
50	chr6:110104633-110104683	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:110119585..110121731-chr6:110123236..110125799,2	K562	blood:
2	chr6:110096444..110098680-chr6:110099797..110102470,2	K562	blood:
3	chr6:110120231..110121949-chr6:110122894..110124736,2	K562	blood:
4	chr6:109847963..109848914-chr6:110104179..110105102,2	K562	blood:
5	chr6:110096444..110098680-chr6:110099797..110102470,2	K562	blood:
6	chr6:110114769..110118657-chr6:110122896..110125381,3	K562	blood:
7	chr6:110120231..110121949-chr6:110122894..110124736,2	K562	blood:
8	chr6:110114769..110118657-chr6:110122896..110125381,3	K562	blood:
9	chr12:52677274..52679079-chr6:110101509..110103009,2	MCF-7	breast:
10	chr6:110119585..110121731-chr6:110123236..110125799,2	K562	blood:
11	chr6:110011565..110014032-chr6:110081170..110083207,2	MCF-7	breast:
12	chr6:110096762..110098535-chr6:110100330..110101952,2	K562	blood:
13	chr6:110096762..110098535-chr6:110100330..110101952,2	K562	blood:
14	chr6:110026116..110027123-chr6:110104149..110105170,4	MCF-7	breast:

Variant related genes	Relation type
FIG4	TF binding region
FIG4	CpG island
ENSG00000112367	chromatin interactions
ENSG00000155085	chromatin interactions

Extended variants
information (count: 2192 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:2192 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12206574	chr6:110067773-110067774	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs112564123	chr6:110067778-110067779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540302173	chr6:110067835-110067836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544567862	chr6:110067859-110067860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116876791	chr6:110067900-110067901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560478359	chr6:110067965-110067966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138199557	chr6:110067979-110067980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149600567	chr6:110067998-110067999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560494211	chr6:110068018-110068019	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144332448	chr6:110068027-110068028	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191495788	chr6:110068084-110068085	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78727540	chr6:110068090-110068091	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140932679	chr6:110068117-110068118	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577128269	chr6:110068135-110068136	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548172885	chr6:110068141-110068142	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143269499	chr6:110068161-110068162	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183736650	chr6:110068205-110068206	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562797347	chr6:110068232-110068233	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527694654	chr6:110068282-110068283	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62437568	chr6:110068292-110068293	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs188797156	chr6:110068294-110068295	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181270123	chr6:110068309-110068310	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs13198852	chr6:110068322-110068323	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs147542047	chr6:110068349-110068350	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116211591	chr6:110068350-110068351	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561341871	chr6:110068372-110068373	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187134487	chr6:110068408-110068409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531448475	chr6:110068468-110068469	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190030494	chr6:110068516-110068517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181616172	chr6:110068517-110068518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563685995	chr6:110068572-110068573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12528392	chr6:110068614-110068615	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs140262784	chr6:110068638-110068639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142054185	chr6:110068648-110068649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563006377	chr6:110068672-110068673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs116958525	chr6:110068719-110068720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6941360	chr6:110068786-110068787	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs186351818	chr6:110068822-110068823	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527543852	chr6:110068854-110068855	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547295205	chr6:110068932-110068933	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369279949	chr6:110068951-110068952	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190752776	chr6:110069025-110069026	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539078487	chr6:110069034-110069035	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555815779	chr6:110069323-110069324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570395229	chr6:110069332-110069333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6922064	chr6:110069350-110069351	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs535210536	chr6:110069453-110069454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6899915	chr6:110069470-110069471	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs574937175	chr6:110069528-110069529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540924498	chr6:110069546-110069547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
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
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	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
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1231 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:110013000-110114400	Weak transcription	Right Ventricle	heart
2	chr6:110028000-110071200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr6:110028200-110080800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr6:110035000-110071400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:110035000-110084000	Weak transcription	GM12878-XiMat	blood
6	chr6:110035200-110094200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr6:110035400-110083000	Weak transcription	Brain Germinal Matrix	brain
8	chr6:110035600-110089000	Weak transcription	Spleen	Spleen
9	chr6:110036800-110115600	Weak transcription	Colonic Mucosa	Colon
10	chr6:110039000-110081000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr6:110041400-110081000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr6:110042200-110088800	Weak transcription	Fetal Intestine Small	intestine
13	chr6:110042400-110089000	Weak transcription	Brain Cingulate Gyrus	brain
14	chr6:110044200-110115400	Weak transcription	Brain Angular Gyrus	brain
15	chr6:110047200-110084000	Weak transcription	Small Intestine	intestine
16	chr6:110047600-110068800	Weak transcription	Dnd41	blood
17	chr6:110048600-110089800	Weak transcription	Fetal Kidney	kidney
18	chr6:110050400-110078400	Weak transcription	Fetal Brain Male	brain
19	chr6:110057200-110089000	Weak transcription	Fetal Brain Female	brain
20	chr6:110057400-110089000	Weak transcription	Esophagus	oesophagus
21	chr6:110057600-110086200	Weak transcription	Brain Anterior Caudate	brain
22	chr6:110058200-110087200	Weak transcription	Rectal Smooth Muscle	rectum
23	chr6:110058200-110089000	Weak transcription	Lung	lung
24	chr6:110058400-110085000	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr6:110058400-110089600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr6:110058800-110112400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr6:110059200-110069400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr6:110059200-110124000	Weak transcription	Colon Smooth Muscle	Colon
29	chr6:110060000-110087800	Weak transcription	Fetal Thymus	thymus
30	chr6:110060400-110068000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:110061200-110089200	Weak transcription	Pancreas	Pancrea
32	chr6:110062600-110089200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr6:110062800-110087400	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr6:110062800-110088000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr6:110063000-110078000	Weak transcription	Primary hematopoietic stem cells	blood
36	chr6:110065200-110084000	Weak transcription	Left Ventricle	heart
37	chr6:110065200-110089000	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr6:110065200-110111200	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr6:110065400-110094200	Weak transcription	Brain Substantia Nigra	brain
40	chr6:110065600-110067800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr6:110065600-110068200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr6:110065600-110069000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr6:110065600-110069200	Weak transcription	Aorta	Aorta
44	chr6:110065600-110069600	Weak transcription	Liver	Liver
45	chr6:110065600-110070000	Weak transcription	Fetal Muscle Trunk	muscle
46	chr6:110065600-110070400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr6:110065600-110073000	Weak transcription	Stomach Smooth Muscle	stomach
48	chr6:110065600-110074200	Weak transcription	Fetal Intestine Large	intestine
49	chr6:110065600-110074400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr6:110065600-110077800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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