Variant report

Variant	nsv830807
Chromosome Location	chr6:131390952-131581931
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1740)
CpG islands
(count:916)
Chromatin interactive
region (count:35)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1740 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:131456357-131456657	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:131428241-131428680	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:131437884-131438290	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:131459690-131459766	K562	blood:	n/a	n/a
5	ARID3A	chr6:131401514-131401532	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:131406182-131406382	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:131504139-131504291	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:131437954-131438268	K562	blood:	n/a	n/a
9	ARID3A	chr6:131457111-131457634	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:131481625-131481806	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:131485073-131485283	HepG2	liver:	n/a	n/a
12	ATF1	chr6:131428317-131428583	K562	blood:	n/a	n/a
13	ATF2	chr6:131520738-131521260	GM12878	blood:	n/a	n/a
14	BACH1	chr6:131456427-131456648	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr6:131429151-131429474	GM12878	blood:	n/a	n/a
16	BATF	chr6:131520913-131521168	GM12878	blood:	n/a	n/a
17	BATF	chr6:131451078-131451303	GM12878	blood:	n/a	chr6:131451179-131451189 chr6:131451178-131451189
18	BATF	chr6:131451051-131451309	GM12878	blood:	n/a	chr6:131451179-131451189 chr6:131451178-131451189
19	BATF	chr6:131428351-131428664	GM12878	blood:	n/a	n/a
20	BCL11A	chr6:131429193-131429588	GM12878	blood:	n/a	n/a
21	BCL11A	chr6:131429194-131429583	GM12878	blood:	n/a	n/a
22	BCL3	chr6:131428190-131428608	A549	lung:	n/a	n/a
23	BCLAF1	chr6:131520780-131521237	GM12878	blood:	n/a	n/a
24	BHLHE40	chr6:131437969-131438269	GM12878	blood:	n/a	n/a
25	BHLHE40	chr6:131520903-131521363	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:131457013-131457179	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:131456349-131457263	HepG2	liver:	n/a	chr6:131456953-131456969 chr6:131456961-131456977
28	BHLHE40	chr6:131429278-131429501	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:131457109-131457125	K562	blood:	n/a	n/a
30	BHLHE40	chr6:131430159-131430902	GM12878	blood:	n/a	n/a
31	BRCA1	chr6:131455939-131456362	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr6:131520861-131521007	GM12878	blood:	n/a	n/a
33	BRCA1	chr6:131456609-131456644	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr6:131456401-131456653	HepG2	liver:	n/a	n/a
35	CBX3	chr6:131456323-131456630	K562	blood:	n/a	n/a
36	CBX3	chr6:131414426-131414792	HCT-116	colon:	n/a	n/a
37	CCNT2	chr6:131428226-131428504	K562	blood:	n/a	n/a
38	CCNT2	chr6:131456367-131457090	K562	blood:	n/a	n/a
39	CEBPB	chr6:131486184-131486378	A549	lung:	n/a	chr6:131486322-131486333
40	CEBPB	chr6:131534127-131534395	A549	lung:	n/a	chr6:131534279-131534290 chr6:131534277-131534294
41	CEBPB	chr6:131552295-131552592	IMR90	lung:	n/a	n/a
42	CEBPB	chr6:131437896-131438198	A549	lung:	n/a	n/a
43	CEBPB	chr6:131534108-131534455	IMR90	lung:	n/a	chr6:131534279-131534290 chr6:131534277-131534294
44	CEBPB	chr6:131428333-131428672	K562	blood:	n/a	chr6:131428501-131428512
45	CEBPB	chr6:131437891-131438251	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr6:131451086-131451422	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:131456011-131456610	A549	lung:	n/a	chr6:131456292-131456305 chr6:131456294-131456305 chr6:131456292-131456303 chr6:131456294-131456305
48	CEBPB	chr6:131552287-131552605	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr6:131576884-131577411	H1-hESC	embryonic stem cell:	n/a	chr6:131576977-131576988
50	CEBPB	chr6:131456218-131456450	H1-hESC	embryonic stem cell:	n/a	chr6:131456292-131456305 chr6:131456294-131456305 chr6:131456292-131456303 chr6:131456294-131456305

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:131456780-131456830	ProgFib	skin:	n/a
2	chr6:131456780-131456830	ProgFib	skin:	n/a
3	chr6:131452754-131452804	HCM	heart:	n/a
4	chr6:131456780-131456830	BJ	skin:	n/a
5	chr6:131484138-131484188	SKMC	muscle:	n/a
6	chr6:131571669-131571719	PANC-1	pancreas:	n/a
7	chr6:131504781-131504831	HNPCEpiC	eye:	n/a
8	chr6:131455450-131455500	HRPEpiC	eye:	n/a
9	chr6:131457146-131457196	HepG2	liver:	n/a
10	chr6:131457146-131457196	HEK293	kidney:	embryo
11	chr6:131481003-131481053	GM12878	blood:	n/a
12	chr6:131461133-131461183	ovcar-3	ovarian:	n/a
13	chr6:131455450-131455500	HRCEpiC	kidney:	n/a
14	chr6:131456785-131456835	H1-hESC	embryonic stem cell:	embryo
15	chr6:131461133-131461183	AG09309	skin:	n/a
16	chr6:131455450-131455500	GM12892	blood:	n/a
17	chr6:131457146-131457196	ovcar-3	ovarian:	n/a
18	chr6:131504781-131504831	GM19239	blood:	n/a
19	chr6:131456780-131456830	GM12891	blood:	n/a
20	chr6:131481003-131481053	A549	lung:	n/a
21	chr6:131452754-131452804	IMR90	lung:	fetal
22	chr6:131457506-131457556	NT2-D1	testis:	n/a
23	chr6:131461133-131461183	HepG2	liver:	n/a
24	chr6:131452754-131452804	GM12891	blood:	n/a
25	chr6:131571669-131571719	BE2_C	brain:	n/a
26	chr6:131452754-131452804	AG09319	gingival:	n/a
27	chr6:131461133-131461183	U87	brain:	n/a
28	chr6:131571669-131571719	BJ	skin:	n/a
29	chr6:131457146-131457196	LNCaP	prostate:	n/a
30	chr6:131456780-131456830	HCM	heart:	n/a
31	chr6:131481003-131481053	AG09309	skin:	n/a
32	chr6:131457506-131457556	HEK293	kidney:	embryo
33	chr6:131456785-131456835	AG10803	skin:	n/a
34	chr6:131455450-131455500	K562	blood:	n/a
35	chr6:131457146-131457196	SAEC	small airway:	n/a
36	chr6:131457506-131457556	HRCEpiC	kidney:	n/a
37	chr6:131457146-131457196	HRPEpiC	eye:	n/a
38	chr6:131456785-131456835	AG04450	lung:	fetal
39	chr6:131455450-131455500	NHDF-neo	bronchial:	n/a
40	chr6:131455450-131455500	HIPEpiC	eye:	n/a
41	chr6:131452754-131452804	NHDF-neo	bronchial:	n/a
42	chr6:131571435-131571485	LNCaP	prostate:	n/a
43	chr6:131457506-131457556	AG09309	skin:	n/a
44	chr6:131456780-131456830	HAEpiC	amniotic membrane:	n/a
45	chr6:131571669-131571719	AG04449	skin:	fetal
46	chr6:131548063-131548113	GM06990	blood:	n/a
47	chr6:131456365-131456415	MCF-7	breast:	n/a
48	chr6:131456365-131456415	HRCEpiC	kidney:	n/a
49	chr6:131571669-131571719	AoSMC	blood vessel:	n/a
50	chr6:131456785-131456835	NHDF-neo	bronchial:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:131205861..131206789-chr6:131437584..131438674,3	MCF-7	breast:
2	chr11:62609119..62609619-chr6:131456326..131457092,2	HCT-116	colon:
3	chr6:131452705..131454330-chr6:131455080..131456599,2	K562	blood:
4	chr15:69744952..69745682-chr6:131456347..131457188,2	Hela-S3	cervix:
5	chr6:131562493..131564861-chr6:131566716..131568915,2	MCF-7	breast:
6	chr6:131453607..131455513-chr6:131455602..131457616,2	MCF-7	breast:
7	chr6:131574679..131577194-chr6:131577773..131580608,2	MCF-7	breast:
8	chr6:131503963..131504691-chr6:131855024..131855989,3	MCF-7	breast:
9	chr6:131482888..131484884-chr6:131488327..131490881,2	MCF-7	breast:
10	chr6:131448808..131452691-chr6:131455777..131458768,3	K562	blood:
11	chr6:131456917..131458462-chr6:131459846..131461723,2	MCF-7	breast:
12	chr6:131443799..131447689-chr6:131455563..131459446,5	K562	blood:
13	chr6:131504234..131504890-chr8:67976530..67977471,2	MCF-7	breast:
14	chr6:131574679..131577194-chr6:131577773..131580608,2	MCF-7	breast:
15	chr6:131482888..131484884-chr6:131488327..131490881,2	MCF-7	breast:
16	chr6:131455097..131458948-chr6:131460458..131462191,4	K562	blood:
17	chr6:131465952..131467796-chr6:131470590..131473026,2	MCF-7	breast:
18	chr6:131206202..131207218-chr6:131437649..131438583,4	MCF-7	breast:
19	chr1:1509737..1510642-chr6:131456190..131456991,2	Hela-S3	cervix:
20	chr6:131451653..131454218-chr6:131455902..131457884,2	MCF-7	breast:
21	chr6:131206207..131207173-chr6:131488628..131489910,7	MCF-7	breast:
22	chr6:131526816..131527805-chr6:131855115..131855774,2	MCF-7	breast:
23	chr6:131206831..131209804-chr6:131436324..131438672,3	MCF-7	breast:
24	chr6:131562493..131564861-chr6:131566716..131568915,2	MCF-7	breast:
25	chr6:131449929..131453503-chr6:131455186..131458213,3	MCF-7	breast:
26	chr6:131456092..131458598-chr6:131462926..131464450,2	K562	blood:
27	chr6:131206634..131207291-chr6:131489082..131489592,2	K562	blood:
28	chr6:131455039..131456597-chr6:131460458..131462514,2	K562	blood:
29	chr6:131456917..131458462-chr6:131459846..131461723,2	MCF-7	breast:
30	chr6:131452705..131454330-chr6:131455080..131456599,2	K562	blood:
31	chr4:105398713..105399471-chr6:131472742..131473607,2	MCF-7	breast:
32	chr6:131445229..131447238-chr6:131455740..131457874,2	K562	blood:
33	chr6:131206179..131207660-chr6:131436807..131438665,12	K562	blood:
34	chr6:131455039..131456597-chr6:131460458..131462514,2	K562	blood:
35	chr6:131526933..131527448-chr6:131918295..131918857,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPB41L2-1	chr6:131447707-131447861	l_3256_chr6:131447706-131492675_testes
2	lnc-EPB41L2-1	chr6:131492570-131492675	l_3256_chr6:131447706-131492675_testes
3	lnc-EPB41L2-1	chr6:131465390-131465456	l_3256_chr6:131447706-131492675_testes

No data

Variant related genes	Relation type
AKAP7	TF binding region
ENSG00000218857	TF binding region
AKAP7	CpG island
ENSG00000218857	CpG island
ENSG00000215014	chromatin interactions
ENSG00000104218	chromatin interactions
ENSG00000118507	chromatin interactions
ENSG00000121022	chromatin interactions
ENSG00000160075	chromatin interactions
ENSG00000137818	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 6122 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:6122 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141228890	chr6:131391186-131391187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536737660	chr6:131391187-131391188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182879269	chr6:131391198-131391199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs951251	chr6:131391212-131391213	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs574267462	chr6:131391219-131391220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs73623827	chr6:131391239-131391240	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs558442559	chr6:131391244-131391245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150337448	chr6:131391287-131391288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543920385	chr6:131391292-131391293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556116212	chr6:131391306-131391307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371231770	chr6:131391406-131391407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538479896	chr6:131391411-131391412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187440506	chr6:131391442-131391443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560263942	chr6:131391491-131391492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528714447	chr6:131391492-131391493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138040675	chr6:131391527-131391528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192955995	chr6:131391546-131391547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570342895	chr6:131391557-131391558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73775910	chr6:131391581-131391582	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs569218026	chr6:131391601-131391602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530159946	chr6:131391623-131391624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184605475	chr6:131391653-131391654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566591792	chr6:131391654-131391655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73623828	chr6:131391658-131391659	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs551624324	chr6:131391720-131391721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558283233	chr6:131391741-131391742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149527897	chr6:131391743-131391744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538128345	chr6:131391759-131391760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187486890	chr6:131391768-131391769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574397049	chr6:131391787-131391788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7740558	chr6:131391789-131391790	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs58237210	chr6:131391827-131391828	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs141556740	chr6:131391838-131391839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575865888	chr6:131391847-131391848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs71905904	chr6:131391849-131391850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75713047	chr6:131391851-131391852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77199413	chr6:131391854-131391855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573652044	chr6:131391858-131391859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200826642	chr6:131391860-131391861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377409645	chr6:131391938-131391939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192086071	chr6:131391985-131391986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537931861	chr6:131391995-131391996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565464365	chr6:131392016-131392017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146036853	chr6:131392185-131392186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555870709	chr6:131392262-131392263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35827051	chr6:131392345-131392346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544866364	chr6:131392379-131392380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563011962	chr6:131392412-131392413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530050496	chr6:131392413-131392414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35404258	chr6:131392418-131392419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2620 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131387200-131392800	Weak transcription	K562	blood
2	chr6:131401400-131401800	Active TSS	HepG2	liver
3	chr6:131401800-131403800	Enhancers	HepG2	liver
4	chr6:131403600-131404000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:131403600-131404400	Enhancers	Rectal Mucosa Donor 29	rectum
6	chr6:131404400-131405400	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr6:131404800-131405600	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr6:131404800-131405600	Enhancers	Stomach Mucosa	stomach
9	chr6:131404800-131405800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr6:131405000-131405600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr6:131405000-131405800	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr6:131405200-131405600	Enhancers	Small Intestine	intestine
13	chr6:131405200-131405800	Enhancers	Fetal Intestine Small	intestine
14	chr6:131405400-131405800	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr6:131405400-131406000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:131406400-131406600	Enhancers	Gastric	stomach
17	chr6:131407400-131407800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:131411000-131411600	Enhancers	Primary B cells from peripheral blood	blood
19	chr6:131411000-131411800	Enhancers	Primary B cells from cord blood	blood
20	chr6:131422000-131422400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:131422200-131424000	Enhancers	Rectal Mucosa Donor 29	rectum
22	chr6:131422400-131423400	Enhancers	Muscle Satellite Cultured Cells	--
23	chr6:131422400-131428000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:131422600-131423600	Enhancers	NH-A	brain
25	chr6:131422600-131424600	Enhancers	HUVEC	blood vessel
26	chr6:131422800-131423000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:131423000-131423400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr6:131423000-131423600	Enhancers	HMEC	breast
29	chr6:131423000-131423600	Enhancers	NHEK	skin
30	chr6:131423000-131423800	Active TSS	A549	lung
31	chr6:131423000-131423800	Enhancers	HSMM	muscle
32	chr6:131423000-131424000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr6:131423000-131425400	Enhancers	Duodenum Mucosa	Duodenum
34	chr6:131423000-131425400	Enhancers	Osteobl	bone
35	chr6:131423000-131426000	Enhancers	Fetal Intestine Large	intestine
36	chr6:131423200-131423400	Enhancers	Fetal Intestine Small	intestine
37	chr6:131423200-131423600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr6:131423200-131424000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr6:131423400-131423800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
40	chr6:131423400-131424400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr6:131423400-131424400	Weak transcription	Fetal Intestine Small	intestine
42	chr6:131423600-131423800	Flanking Active TSS	NH-A	brain
43	chr6:131423600-131428000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr6:131423600-131428000	Weak transcription	NHEK	skin
45	chr6:131423800-131424000	Enhancers	NH-A	brain
46	chr6:131423800-131424200	Enhancers	Muscle Satellite Cultured Cells	--
47	chr6:131423800-131424400	Flanking Active TSS	A549	lung
48	chr6:131423800-131428000	Weak transcription	HSMM	muscle
49	chr6:131424000-131424200	Flanking Active TSS	NH-A	brain
50	chr6:131424000-131425600	Enhancers	HepG2	liver

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